Post Inaugural Disability Awareness Month

AES Post Inaugural Campus-Wide Disability Awareness Month 2024

"Beyond Awareness: Nurturing an Accessible Educational Community"

We are delighted to announce the successful completion of the Inaugural Disability Awareness Month, organized by the Division of Diversity, Equity, and Inclusion’s Office of Accessible Educational Services (AES). This month-long celebration featured various activities, including a kick-off luncheon, keynote speeches, games, tabling, panel discussions, technology demonstrations, equity stories, and a mini-resource fair. We sincerely thank everyone who contributed to this event's success. Your dedication and support were invaluable. Participant feedback highlighted the sessions' value and the strong sense of community fostered throughout the month. This event marks the beginning of our journey towards creating a more outward-facing and collaborative Accessible Educational Services Community of Practice (AESCoP). This initiative aims to unify existing relationships and services to advocate for disabled students and students with disabilities, fostering a sense of belonging at IU Indianapolis.


Intent: Our goal was to create an inclusive platform to recognize and celebrate the experiences of disabled students and students with disabilities. Throughout the month, we hosted various events in collaboration with students, faculty, staff, and internal and external partners to foster a sense of community and belonging actively.


Impact: This celebration laid the groundwork for moving beyond disability awareness to nurturing a community that humanizes individuals, provides access, amplifies voices through advocacy, and promotes justice through disability rights and a disability justice framework. We are fostering continual relationships by building and growing together within our existing relationships and services. We aim to create an AESCoP that aligns with IU Indianapolis’s 2030 goals and values. We invite all on-campus and off-campus community members—students, faculty, staff, and partners—to join us in this journey, contribute their unique perspectives, and actively build a more inclusive and supportive environment. Your participation is crucial to our IU Indianapolis community's growth and success. Together, we can make a lasting impact.

Indiana University Indianapolis Accessible Educational Services Director, Dr. Mercedes A. Cannon.

“This was a fantastic event and I hope to bring others with me next year! Good work!” -participant

AES in DEI: Inaugural Disability Awareness Month Opening Celebration

 

Games Event

Intent: The intent of the games event was to bring awareness to the campus that accessible games exist and to create an inclusive space for belongingness centered around games and activities.

Impact: This event was informative for the attendees to gain better understanding of what accessibility in activities can look like, physically and virtually. It brought together the AES staff and student groups (centered around disability) to collaborate and grow relationships. It helped spark new ideas for AES and DEI staff for future events and meetups.

Three people play accessible uno and in the background two people play a tactile game
AES director talks to ATAC staff members at tactile game station
student sits at a table to color a disability activism coloring page

Luncheon and Guest Speaker Event

In March 2024, the Division of Diversity, Equity & Inclusion’s Office of Accessible Educational Services (AES) hosted the Inaugural Campus-Wide Disability Awareness Month at IU Indianapolis (IUI). This month-long celebration was designed to honor the experiences of disabled students here at IUI and highlight AES's ongoing commitment to inclusion and advocacy. The event featured various activities, including a kick-off luncheon, keynote addresses, games, information sessions, and a mini-resource fair. Dr. Tiffany Kyser was the Mistress of Ceremony, leading the day eloquently and authentically. At the same time, the director of AES emphasized the importance of collaborative efforts in fostering inclusion with the slogan, "Nothing about us without us." Keynote speaker Dr. Betts challenged attendees with her powerful words that connected with the audience participants with and without disabilities.

AES envisions the future of fostering conversations, hosting panel discussions, and engaging the campus community in justice-oriented dialogues that nurture an inclusive and accessible educational environment.

View of speaker, Dr. Katherine Betts, in her speech, with sign reading Disability Awareness Month in red, and ASL interpreter on the right
Three attendees at their table, all members of ATAC, looking on with eager expressions
View of well dressed attendees engrossed in discussion
Side view of Director of AES, Dr. Mercedes Cannon, giving her introduction smiling with glasses on and ASL interpreter mid sentence
Two well dressed women smile as they select lunch options
View from the back of the luncheon shows attendees finishing up lunch and Dr. Tiffany Kaiser beginning the intro with screen behind her of the recording
View from behind some attendees as they look to the speaker, Katherine Betts, mid sentence in front of a microphone
Three well dressed attendees stand in half circle engrossed in conversation
View from the side of the well attended luncheon shows the speaker standing at the microphone and an ASL interpreter standing next to her

Description of the video:

President George HW. Bush signed into law on July 20 sixth. So who's this person speaking with you today and launch right into it as I do. My name is Dr. Tiffany Kaiser. She her  not at all necessary. I am an iu PY alum.  I serve as the executive Director of Outreach and Engagement for the Indiana University Alumni Association. But it is truly my deep privilege to serve as mistress of ceremonies for today's event.  as we gather, know that I and Miss Kimberly Merritt, managing Director of Alumni relations within the iupy office of alumni relations, Kim, if you would mind rising or just signaling  that we're also here to learn with and from future and current alum.  including, but moving beyond our individual growth  towards systemic changes, and how the Iu Alumni Association recognizes difference in our work, centering disability at the intersections for all, for all iupy campuses and all Iu campuses, regional centers and international chapters. Indeed, we seek to move beyond awareness of disability, to redressing ableist policies and practices.  So again, we want to welcome you and welcome specifically to in terms of my role and Kim's role, that 31 alum who join us today  as we an educational community grapple with the future of attendant care funding in Indiana  and its impact on people with disabilities and their families. As we continue to mourn the loss of Judith, Judy Hume. widely regarded as the mother of the Disability rights movement.  who passed one year ago today, exactly  on the afternoon of March fourth, 2023, at the age of 75, in Washington, DC. Full circle where the crawl took place.  As we continue to deal with the loss of so many of our 4 mothers, such as Bell Hooks.  Gwendolyn, Brooks. Toni Morrison. and the recent harm and loss of black women in the Academy negotiating, unwelcoming, and hostile environments.  It is important to be explicit here, on my understanding of the definition of Ableism that perhaps may serve this collective today. Orbiter, Pratt, and Minoti. in last year's chapter, Disabled Lives. Worthiness and Identity, and enable a society within the text, sustaining disabled youth, considering disability and asset pedagogies. co-edited by Dr. Frederico Weitler. an Iu school of Education's Doctor Kathleen King Torus.  Professor of special education and urban education studies and founding executive director of the Great Lakes. Equity Center notes in this definition  a broad definition of ableism  is a system that places value on people's bodies and minds based on societally constructed ideas of normality. intelligence, excellence, desirability, and productivity. Bogart and Dunn described this as stereotyping prejudice, discrimination and social oppression toward people with disabilities more specific to the education. Space here describes. Ableism as quote the devaluation of disability that results in societal attitudes that uncritically assert  that it is better for a child to walk than roll. Speak, then sign.  read, print, then read Braille. spell independently, then use a spell, check and hang out with non-disabled kids as opposed to other disabled kids. Nario Redman takes this further by characterizing different types of Ableism as hostile. benevolent. and ambivalent.  These ableist notions range from the outwardly hostile. such as hate crimes that are committed because of one's disability to more subtle expressions, such as paternalistic overprotection  or praise for everyday activities  end, quote  additionally as a temporarily abled cisgendered female. We are black woman entering this conversation. This space and the disability, justice, space with privilege.  As I attempt to work in scholarship and practice towards solidarity. I hold my commitment to critical consciousness for myself and the organizations I work within.  near in both my learning and action. I want to say that again, as someone privileged  in the disability space and forging towards disability justice.  I hold near my work to hold my individual critical consciousness and that of critical conscious organizations that I work with them, that I hold near.  So an announce acknowledgement of other intersectional awareness. Months as we push to move beyond awareness gathering today, I hope that we recognize the deliberate effort required to move beyond awareness and foster a sense of belonging within our community. : Adaptive educational services or Aes's aim is to cultivate an accessible educational environment : that embraces both perceivable and non perceivable disabled individuals as well as people with disabilities here on the Iu Indianapolis campus. : Furthermore, we gather today encouraging, moving beyond awareness. For March 20 twenty-four's developmental disabilities. Awareness month. We also acknowledge and integrate April's autism, awareness and Acceptance month. : May's Mental health Awareness, month and July is disability, pride, awareness, Month. including additional awareness months at the intersections  was a lot. : I now want to move to introducing Dr. Karen, base Vice Chancellor for diversity, equity, and inclusion to provide an additional welcome. Please join me in welcoming Dr. Dave. : Good afternoon. It is my honor : to welcome you to the Kickoff luncheon of the inaugural campus. Wide disability, awareness, month activities here at Iui.  the theme beyond awareness. nurturing, accessible, educational and accessible educational community says everything you need to know about accessible educational services. And IUPU. I.  And the team here, led by Dr. Mercedes cannon. Throughout the month you will have an opportunity to hear from undergraduate and graduate student panelists about their academic journeys attend a mini resource, fair engage in assistive technology demonstrations as well as hear from today's keynote speaker, Doctor Katherine Betts.  the professionals making up accessible educational services are dedicated to ensuring that every student they serve the inaugural campus. Fine disability awareness.  today I will share a brief history of Aes  crawling on my experiences.  there we drawing on my experiences as a student professional who has worked with Aes office since 2,009. But first.  I must express  my deep appreciation and admiration for our incredible Aes team. including our office staff. Natalie Albert Lance, Dr. Elena Silverman.  Marcia Stevenson. Alex Nixon.Alicia MacDonald, Jonathan step in in the back  and are wonderful interpreters. Patty Nwahap and Jean Runley.  Yes, thank you. Hmm! In spite of the tight timeline.  Now your dedication and passion have been the foundation of our success.  and bringing the vision of disability awareness month to mind. Thank you.  Now, everyone else. As you enter the luncheon, I hope you noticed that the Ada Crawl Video.  taking us on a journey through the past, as we gather, to celebrate March 2024,  which marks the thirty-seventh  anniversary of national developmental disability. Awareness Month. where President Ronald Reagan officially established this month with Proclamation 56, 13. On February the 20 seventh, 1987, which increased awareness  by urging Americans to support individuals with developmental disabilities as we work to foster understanding.  acceptance  and inclusion in various aspects of community life. So as I turn my gaze to the history of Aes. I share my unique perspective. Working in adaptive educational services as a non-traditional black student turned professional  with a speech and language impairment that emerged from a childhood trauma.  In doing so I do identify with person first language. which means I'm a person with a disability.  In 2,009 I met Pam King, the director of adaptive educational services.  Aes. This was at the onset of my undergraduate education. As I prepared to begin my graduate work and my struggles to navigate, written and spoken centre.  Pam was the third director of Iupui's Disability student services. The Ss. Office. S. Aes. Was called then.  and she assumed her role in October, 1989 as a rehabilitation counselor. This was just a year before the enactment of the Americans with disability at 88 and 1990,  which was the groundbreaking legislation, and showing equal opportunities and access to higher education for individuals with disabilities.  Pam dedicated herself to facilitating reasonable accommodations and fostering at this student participation under her leadership, the renaming of Vss to adaptive educational services. reflecting the importance of students, voices, and input in our name  also emphasize, emphasize  education, central role in our work and essential walls with changes in higher education, landscape mainly influenced by input from black student Union and Vice Chancellor Whitney  Aes was then moved to reside within the newly established diversity, equity, and inclusion division. and after 25 years of leadership, Pam retired in December of 2,017,  I stepped into the role as an interim director. On January first, 2,018, I was a student professional, who continued to value our student centered approach to mentoring and serving students.  In fact, my office had developed into a haven for students to hang out and discuss their education and campus  as interim. I prioritize our office, professional development and advancement. As I work with Hr. To restructure one of our most important positions hire new support staff to fill position gaps  and created an environment within which our staff's confidence could grow.  We welcomed Dr. Kevin Mccracken as our new director. In the fall of 2,018,  Kevin picked up the manual of Leadership and he's finished fill filling in the hiring gaps. Establish the 3 step process for students registration. But yeah, services  and transitioned us to using accommodate software  which increase effective efficiency for office  as associate director. I've provided Kevin with insights into campus networks and orientation to disability services  haven't offered me his guidance on management and leadership.  allowing us to bridge knowledge gaps that remain beneficial to us the day  our relationship evolved into a reciprocal mentor mentee collaboration.  fostering a collegiable and mutual, respectful working, planning.  Our conversations expanded into identity, race, privilege.  equity, and so in society.  enhancing our mutual understanding.  he was dedicated to educating iup us campus on aes processes.  The significance of Ada work  and advocating on behalf of our students receiving our services.  Kevin's Moto, I'm a motto  was gentle pressure relentlessly applied.  Continue this. This model continues to shape our office. Depos in the summer of 2,023, the Aes office name change to accessible educational services Aes.  which retains the familiar acronym, but infuses our work with renew.  In July 2023, Dr. Kevin Mccracken moved on to become a clinical Assistant Professor of Psychology and Mental Health Counseling  and Director of Clinical Training at Iu. Columbus.  and the assistant director, Natalie Albert, became the interim director, 3 for 3 months.  In the summer of 2,022, I departed. A. Yes, to join Syracuse University, as the postdoc in their center on disability and inclusion.  During my time at Syracuse, I learned much about the importance of ensuring our commitment to inclusion, establishing a sense of belonging and equity, and all the work that we do to advocate for students we serve.  Then, on October the fifth, 2023,  I began my appointment as the director of a. Yes.  here at IUPU. I ui.  My live and professional experiences, as well as my scholarship, remain utter, most important in my mind, and as I work to ensure that we honor and value the dignity of disabled students and students with disabilities in higher education.  Additionally, I continue to prioritize our wonderful aes staff, honoring our strong relationships, built on trust.  inclusion, and equity. that moves us beyond simple awareness to nurturing and establishing an accessible educational community of practice.  This community will center building collaborative relationships as we explore and inspire further advocacy with disabled students and students, with disabilities  through respecting and addressing the real world challenges our students face that require inspired creative resistance and inclusive strategies and solutions.  The work is necessary if we truly wish to establish  equitable campus environments that ensure our students can do their best work and achieve their goals.  I'll leave you with this statement.  nothing about us without us echoing the essence of inclusion as it will take building a space of collaboration across constituents. constituencies, as we include everyone's voice  voices and perspectives. Thank you so much.  Good afternoon. Good afternoon. Can everyone hear me? Wonderful? So first of all, I want to say thank you to Dr. Canon and the Aes team for extending this opportunity to me.  I wanna say thank you to aes. And the division of Dei for helping to make sure that I ui has begun in the celebration of this historic event. So first of all, can we just give it up for ourselves? This is a huge event.  This is yes.  this is a demonstrative step of I ui to center the lived experiences of disability, and to do so in a way that honors our lived histories, that connect disability to diversity, and this is a very proud moment. I'm sure, not only for myself, but for all of us in the room. I also want to  acknowledge and say Thank you, because great work does not happen in isolation. But it happens in community. And so we have a phenomenal divisional leader who believed in Dr. Kandin's vision. And the way new initiatives start is that your your senior leader has to be willing to help move it forward. So I want to acknowledge Dr. Dace.  I want to. Yes.  I also want to acknowledge the collaboration. And behind the scenes work of Directors Karina Gardena and Lee, Petrusca and the Multicultural Center and the Lgbtq Center working in collaboration with A. S to make sure that today is a success, and we look forward to many, many more collaborations such as this. So thank you again, Karina and Lee, for your leadership, and making sure that we were here to support.  Thank you. So I was asked to share a little bit about my personal journey and to kind of give us some things to think about as we began to move into celebrating disability awareness month, and moving our institution forward. In a community of practice.  So I always start with this, and I'll leave with this, and it may be very obvious. But  I show up in the world as a black woman with a disability. And this is important to note, because the socially constructed identities are how the world views me, and it has created the lens in which I have had to navigate and view the world. So  I am from Memphis, Tennessee, and and once I get into my store you'll know that I've I've moved lots of pay places. And so people are like, well, where are you? Actually from? I'm from Goodall, Memphis, Tennessee.  where I grew up in the the late eighties, but grew up, having a very positive a very positive and cultural grounding of who I am is a black girl. As a black woman I grew up around black leaders, black teachers.  black religious leaders which you know all of these different experiences help me to walk in and believe in that. My opportunities as a black woman, and at that time as a black girl, were limitless. Despite the history of racism. Right?  However, I have intersecting identity. So I have a disability, and II wanna interject here that my mother who raised me for the most part of my life as a single mother. My mother also has a disability, she is also visually impaired. So in her last year of college she she lost her vision. She had a there was a  epidemic of German measles happening on her campus, and she lost her vision. And so why? This is important. Is because my mother and I were the 2 people in our family at this time who had physical disabilities.  And so this definitely shaped part of my identity. And so one of the things that II ask people to think about when we're talking about how disabilities shaped your identity and and communities in Co communities of color or other marginalized groups. There are some cultural nuances around how we view disability.  And so in my family, while everyone was was well meeting and still believe that you know the world was mine. We didn't always my grandparents and and my mother siblings my cousins. At this time they were really small, like I was, but they didn't really have the knowledge or the education to understand what the resources were to understand what the possibilities were, and so  they were well meaning, but sometimes they were over protective, sometimes they unattentionally, you know, cause harm because we are conditioned from the day we're born we are shaped to think about this ability in certain ways, and until you have an opportunity to reframe your lens. You don't know what you know until you know what you know.  And so at a certain point my mother went through a divorce and she made a decision  that she wanted. She wanted to definitely protect the level of experiences that I was have growing up, and the things that I would be exposed to when she wanted to manage a little bit some of the over protectiveness that was happening from like her parents and her siblings. And so she made the decision that we were going to move to California.  So we moved to California in the late eighties, and California was known to be very liberal, very, you know, very diverse, which it was so I went from kind of like a world view of understanding diversity in terms of black and white around race to really my worldview expanding.  Ii was exposed to lots of diversity at a young age, and I did have  more opportunities. My first time traveling abroad was in high school. My first time going to Washington, DC. Was in Junior High school. However, I will learn that the systems of oppression, such as racism and ableism, don't stop when you get to California.  So I had my first experience with ableism and racism. Going into high school.  So I so people in the room who have experience, special education. This will be familiar. So I went to what was called at that time mainstream classroom classes, but I had a  special education teacher who made sure I had reasonable accommodations. Top braille all of these different things. Iaps which I hate to this day.  Make sure all of those things were in place for me, so I would notice that when I would talk about college, you know, because I was getting ready to. I was doing my schedule for high school, and I grew up. You know, you're gonna go to college. My mother graduated from Tennessee State. So  I grew up thinking I'm going to college. And so when I talk about oh, you know, I need to sign up for these college preparatory classes, she was like, well.  people like you usually go to community college, or you know, maybe you know not. Right now you should go to community college first, and I would be like. Hmm.  you know, like I didn't have the knowledge that I have today to understand what she was saying, and to know that something was wrong, and then she went even further, and she arbitrarily removed me from college preparatory classes that my mother and I had selected, based on my grades and everything else, and she put me in remedial classes.  and nobody in the educational system pushed back. But she was given a lot of power. It was assumed. You work with blind students. You know what's best. This is okay.  So I knew enough to go home and tell my mother what happened. and I won't get into the detail.  but it's nothing like having an advocate, a mama in your corner. She got all of it together, all of it.  So she was a tremendous advocate for me. She addressed the inequities, and I wanna pause here and in address and address what the inequity is because  I noticed that, you know, I'm using word community college. The issue is not that community. College is bad. Community. College is a phenomenal gateway to higher education. However, when someone says to you because you fit these black boxes. You can't because you're black, because you have a disability because you are poor, you don't, or you should not have access  to college. You should go to community college first, or if you wanna think of other types of discrimination, you shouldn't have access to the loan. You shouldn't have access to the job. You all know what I'm saying.  Right? So  what is the inequity that was being addressed? And this, the school system was complicit, and I'll try to hold on to complicity because we're gonna come back to it at the end of this talk  and so fast forward. I did go to college. I went to California State University, Chico, as mentioned in my bio and college, was an amazing place of liberation, and it was also a space of struggle for me.  I'm sorry you got. My glasses are loose.  So it was a place of liberation, because college is where I found my voice as an activist, as a student leader. So Chico was A was considered to be kind of a rural part of California. So there may have been at the time. Was there about 200 black students in a population of 13,000 students.  So we you know we were own community along with other Co. He's historically under represented communities and at Chico State. During this time this was the late nineties going into the early 2 thousands. We didn't have a multi-cultural center. We might have had a room  with no staff and faculty, but we didn't have. We have the Eop office, which is academic wraparound services. We had disability support services. But as far as other types of engagement that reflected our cultural backgrounds, us as student leaders made it happen on that campus.  And so it was wonderful for me, because I had to one learn how to not only speak up for black students and students with disabilities. But I had to learn how to learn about other people's identities through their lens and build coalitions. So this was a great experience. And I wanna also note that there was really nothing to cultivate my experience as a student with disability. We had disability support services, but nothing  to nurture, and the way that we have very intentional ways of nurturing  historically underrepresented students on college, and there was nothing for students with disabilities. So I took these concerns, and we address them in our students spaces when we talked about other inequities. So this is where that passion and that work began for me.  College was a place of struggle. Because so I shared earlier that my mother had a disability. She was legally blind.  and while my mother was a fierce advocate for me. I watched my mother over the majority of my lifetime. A brilliant college, educated black woman, not be able to get a job.  I watch her experience. Discrimination after discrimination, obstacle after obstacle, while she's pushing me.  And so, you know, when I got to college, she got her first job with the Federal Government the year that I went to college, and I was really like, Oh, my God!  Like yes. Finally, because  inside I was kind of terrified of like what is gonna be waiting for me beyond college, and not to say that there were not people who were with disabilities, or people who are blind that had jobs didn't have job because there were. But I'm talking about my own personal experience. So because I didn't know what was waiting for me, and it was kind of rooted in fear that not everyone could relate to decided to. It's name College.  I flunked out.  I had to appeal to get back in. I changed my major 1,000 times, like all of these different themes that were rooted in fear. And so I'll interject this. Here we sometimes come in contact with students who are not  I'm gonna say this in quote the model typical student, high Gpa leadership trajectory that we read about in the textbooks. But we have to. If we're called to support students, we have to figure out what is going on and figure out how to be present with them, cause you really don't know who may be before you.  So all that to say I did come in contact with a mentor in college which actually shifted the trajectory of my of my life. His name is Dr. Pedro Douglas.  He's a member of Alpha Phi Alpha Fraternity Incorporated. So I mentioned, or was mentioned in my resume, that I'm a member, a proud member of already Incorporated.  So why, this is it's important is, Pedro was the director of the Student Health Center. I was gonna go to the doctor. I probably wasn't gonna meet Pedro just in general, because I wouldn't have the need to go to the health Center, but I met Pedro  at a Greek event. He was a new person in town. I met him at a Greek event, and so building connections to students in the room and becoming involved on campus is vitally important. So I met Pedro. He was like, hey? I got a program. I think you it might be good for you. Come through my office and holler at me. I'm like that.  So I go to Pedro's office.  I go to Pedro's office, and so we start to talk about my college journey and career, and you know I have been overly involved as a student. I also like to sing at this time, and I was going different places. We had a gospel choir like he was like, well, you can't see your way through life. What are you gonna do after college? And I was like, II don't know.  And he was like, well, what about graduate school? And I was like Pedro?  I can barely barely get out of voice. Say, University, Chico, II wanna remind you all I was disqualified from the university, and I mean you have to, for people who've never been to that you have to apply and appeal to get back in. So that means you did not do what you're supposed to do on academic probation. Sound like I can barely get through. What do you mean? You want me to go graduate school. He's like, listen, you are not the only person to be on academic probation. Let's create a plan.  And we did. And he invited me to a program that still exists today. It is called the NASA Undergraduate Fellows Program. So any people in the room who know what NASA is. It is a student affairs, higher education organization. It is a wonderful organization. This program, in particular, is a pipeline program  to develop professionals and a professional pipeline of historically under represented professionals within NASA, including disability. So I got an internship. He took a group of us to the NASA Conference, and that really shifted the trajectory of my life. So I went on to go to graduate school. II helped several full time positions. II recently got my doctorate degree.  But this is, you know, II realized that I wanted to provide for students and even staff what Pedro provided for me.  which is why, you know, I kind of feel called to higher education and call to Dei being in these roles, though, as a black woman with a disability has not been easy.  It has been a journey. It has been a 1516 year journey, and many places that I have worked or gone to school. I have been the first person or the only person that was black.  and definitely the first and only person that was a disability that had a disability in these spaces.  So what this meant was that I had to. Whether I wanted to or not, I had to teach people. I had to be relational around what it means to to break down barriers and have people think about disability, because, you know, they had a colleague. And so, you know, human connection is important. You think about things differently. When you humanize people's experience. I had to figure things out in real time, when accommodations were not  appropriate or not existing.  I have faced downright hostility and discrimination, but I've also had a very rewarding career. So you know, these are just a few highlights from my journey. This is kind of how I made my way to Iui  but to make this make even more sense because we're we're very scholarly into place. I wanna put some data before us  for all the scholars in a room to think about.  So. We have approximately one in 4 individuals in the Us. Identified as a person with a disability.  one in 4, that is about 20, maybe a little bit more. That is a large amount of people. So I want you to keep that in mind. According to the Us. Department of Labor, this is 2,023 data.  Roughly, a little bit over 22% of people with disabilities are employed.  Gonna let that sit right there.  22 in the State of Indiana. The latest data I could find was 2,018 in the State of Indiana.  37% of people with disabilities were employed as compared to 80% of non-disabled people.  So just think about the poverty and the educational disparity and all the things that we know happen around high unemployment rates. And we're not even talking about a career pipeline. We're not talking about professional positions versus staff position. So  if if the number for people who are with disabilities, is 22 for people who are employed. Just imagine what that number would be for professional positions or executive positions  in higher education.  in higher education, one in 5 students. Has a disability. When they come to college.  Of this number, there's again a fairly large percentage where you're talking about numbers  37% of these students self disclose having a disability, and for anyone that provides reasonable accommodations in the room, you know that when you switch from secondary to higher education you must self disclose. So you know, we have to ask ourselves why only 37%.  So of the people who do self-disclose and maybe go to Aes or a Disability support Services Office on another camp only between 15 and 45 of those people utilize the accommodations that are offered to them.  That's another question, something else to me feel like, hmm, why is that?  Let's talk about graduation rates. So the graduation rate of students with a disability is 49 versus student without a disability is 68.  So there is a disparity there in how long it's taking people to graduate. Another thing that we study in higher education we talk about belonging  belonging is very important. We know there's there's research out there that says when students feel like they belong, they're they're more successful. Academically, they feel like they, they are a part of campus and they develop leadership skills. They develop all of these wonderful skills to prepare them for work beyond college. So in a study taken in 2021 54,000 college students.  students with disabilities reported billing significantly, had a significant, less sense of belonging than students without disabilities, and these students, with disabilities reported, experiencing a higher level of discrimination on campus.  So why is all of this data, important as we consider ableism and and what how it plays out. So higher education is really the gateway to shifting culture, not only in in college. But you know, we influence so many different fields. So first of all.  the data shows that we don't have enough students with disabilities  graduating and thriving in college. And so we have to ask, like, what is going on to impede their sense of belonging, that is, is, slowing down their graduation rate that is causing them to not self identify like what is happening in the environment. But also we have students who are coming in without disabilities, who are supposed to learn in their college experience how to interrogate stereotypes.  how to interrogate bias.  how to shift their lens to what they maybe have learned prior to college about disability to shifting to a different level of understanding. Because  college graduates are going to be decision makers, social workers, educators, they're gonna decide where funds go. So we need people to learn while they're in college. So this data tells me I don't know what it tells you, but it tells me that in higher education we have serious work to do.  So Dr. Kaiser gave us an amazing definition of ableism, and I think a lot of this is just embedded in the systems of ableism and and the absence of the voices of the disability community in higher education. But just to refresh your memory. So Ableism is steeped in power similar to racism, sexism. All of these different forms of oppression and ableism simply upholds  able-bodiedness as the norm and seeks to fix people with disabilities rather than acknowledging  that having a disability is okay, and that we don't have to just subscribe to these norms. And so this is where some of the microaggressions and cold climate and just absence of the literature about disability comes is steeped in Ableism. And we know that in higher education we're built on exclusion  exclusionary practices which are still influencing. How people experience the institution. And I talked about this in an event last week around black women, and we know that for many many of us.  higher education has not been created to fit our identities as people with disabilities, let alone other identities.  So as we consider a community of practice that will kind of guide our philosophy here at Iui. And my hope is that not only will it guide our philosophy here, but it will reach the system. It will reach other places. Dr. Cannon will be leading that work. But I want to offer us a couple of things to think about.  So number one is we first have to own  it's not anybody's spot on the room. But we have to own and acknowledge that we have structures of Ableism on our campus.  We do, we have to own and acknowledge, and we have to speak to  really like kind of think through where this is and how to dismantle it.  Number 2 is we have to develop a disability community.  And we we have people with a disability. We have people who identify with disabilities on campus and around campus, but in higher education. Many of us in the room know this. We develop communities in very unique ways. And we do that because we know that people need support. And sometimes there's in group support. And then there's being able to work across  and so we have to create a space where we can create a community to elevate the voices of the of us who are in the disability community and create a space to speak to truth, to power about our experiences, create a space to learn from one another and to create a space to offer feedback and be a part of the university process. So we have to intentionally create a disability. Community  number 3 is we have to explicitly begin to articulate  disability justice. And talk about Ableism through a Dei lens. And I talk about a Dei lens a lot. But we. We have to think about privilege, power, and oppression, and how it? How it works. When we talk about Ableism. We have to create be specific in plans and in climate surveys and in trainings one, so that the disability community sees themselves  exclusively name so that we see ourselves in these initiatives, but also so that we can begin to do the work to understand how we can educate our campus and how we can shift the culture of our campus when it comes to disability. Justice  number 5, I think this is Number 5 is coalition building. So coalition building is vitally important that we have to, as a disability community, be able to work  interconnectedly with other underrepresented communities on this campus. I tell people all that all the time that to end one form of oppression we must work to end them all.  and injustice anywhere is injustice everywhere.  So this is the work that we have to engage in.  So, as I prepare to close, I do want to say a couple of words to our students with disabilities in the room. It's something that all students can can be gleam from. But we're centering disability today. So first of all, I want to encourage you students, if you are here on Zoom or in the room, that you have a voice  that you have a voice, and your voice will carry further than ours as administrators ever will.  And being able to articulate what you need, being able to talk about what a holistic student experience looks like for you, because it is important. Research says that's important.  Go back going back to that belonging piece again, being able to cultivate relationships and learn how to lead organization and being able to articulate what you need as a student leader. Those things are very critical, and they transfer to work beyond college. Ask me how I know.  so I want to encourage you to use your voice and  help the institution to move beyond just the work of the Ada. The Ada is a wonderful piece of legislation, but one of the things that we know from the work that we do in Dei is that legislation alone, just saying that you can be here, or that you can have the accommodations to be here. That is not enough. That is the floor, not the ceiling of the work. We want people to feel included, and to be able to show up authentically as our full sales. That is what we want for every person at Iui.  Finally.  this is a call in to all of us that are part of the Iui community. So I want to commend this again for the wonderful work that we are doing and the legacy we're building on. But now I want to ask us what will we do next? So all of us have heard of my story. So if you know, you at least have one personal story to connect to. And we have people at different levels.  In the room and on zoom, who have different levels of influence. So what will you do the next time? There is a policy, or the next time there is a place where you need to be an advocate, because you now have heard you learn more. So when we learn more, we're responsible to do more with what we learn. And I wanna take us back to that data  that I shared earlier. And if we would, most of us would think of that. Data is kind of abysmal. And we have the ability to impact that data and to change the narrative of higher education and disability. One person at a time here at Iui. Thank you  another round of applause for Dr. Betts.  my favorite, my favorite line was that  that  Dr. Best? Thank you so much for your remarks and for sharing your story, and for being vulnerable, to lift up your story, and lived experience as a platform for change and for learning. Thank you.  Dr. Bash, you are a recent contributor  to the second volume of Disabled Faculty and staff, intersecting Identities and higher Education, co-edited by Dr. Mary Lee Vance  and Dr. Elizabeth G. Harrison.  The book covers. Excuse me. The book cover makes a profound statement.  and demonstrating that members of the disability community do not perceive themselves reflected within the faculty. And for those that may not have received this book cover.  it's it's an image. It's an illustrative image  of a a figure looking into a sort of a reflective surface and having some dissonant.  So it's an illustrative portrait of someone I perceive to more be more feminine presenting  looking into a reflective surface. And there's some there's some it's in it. There's an abstraction  based on current research. It can also be argued that students with disabilities  do not perceive themselves reflected within higher education, and you spoke a little bit to that.  and that, furthermore, faculty and staff do not perceive themselves within higher education. The editor of the book makes a statement that all the authors have shared perspectives of their experiences as perceived by their own lenses.  But readers who read these stories through their own lenses for us in this physical space, or in the virtual space we are taking in your story through our own lenses.  rather through the lenses of the author rather than of you telling your story?  Why is it important that people move beyond their own socially constructed lenses, ie. Us, and the physical space in the virtual space where we're either taking in text or either taking in lived experiences  from persons with disabilities, and begin to understand disability and ableism through the lens of people with disabilities rather than our own if we're temporarily able.  Why is this crucially important? I just want to kick us off with that question  cool. This is a great question. So I think that it's important for us to understand disability or any identity. But we're talking about disability today from the perspective of the person  in the community. So if I did not have the identity of a person with a disability, and I saw, you know, chose to look through my lens. My lens might be aplist.  It may, you know, I may not have yet deconstructed my work. It's always  good when you're hearing people's stories to really try to imagine from their point of view. And I think I'm gonna say sometimes when talking about disability, because there's so much stigma around it, it is easy for people to kind of fall into that place of dissonance that that book cover described, and  and so  to not put themselves in the situation, be like, oh, they're just. They're they're being too much. They're being too dramatic, or, you know, it really can't be that bad.  But I think that if we have to do the work of  dismantling. How we have been programmed to think about disability. And this can be for people in a disability community, too, just because we have disabilities does not mean that we can't be able list at the same time, because we still have access to the same socially constructed norms that society has taught us about disabilities. So I think in order to really understand  a situation from the perspective of someone outside of the identity that we don't hold. We have to really be intentional about trying to view the situation through their cultural lens.  Thank you, Dr. Vets, I appreciate it. I've got one more question just to warm up the room, and then we'll open up to the physical and the virtual space. My next question is some of your remarks, well, most of your marks were really underpinned, and how you were reared, and that that rearing, I infer Doctor Bets was from a posture of abundance  of joy, particularly black joy. And I wonder if you can speak to how that is crucial in sustaining and fortifying oneself  as you're negotiating multiple and intersecting forms of oppression. Yes, thank you. Well, first of all, I'm glad that that carried over, because that that is definitely I was raised to value.  to be joyful to value, to be resilient, and that has carried me through some very challenging times as an adult.  I think when I think about my career and some of the hurdles that I've had to overcome.  I had to really remind myself of who I was and go back to my childhood of you know what was instilled in me. What what strategies I was taught like when you feel like your back is against the wall, of how to get yourself back to that place of experiencing black joy and experiencing your faith, because life style here  and at times it desires to not just knock you down, but to lay you out. And when you are navigating spaces.  that where you have multiple identities and you like well, I don't know if this hostility is because I'm black. Is it because I'm a woman, or is it because I'm a dis? I have a disability, or is it all 3 like when you don't know where it is coming from and how to get your grounding. You have to pull from something, or the situation will take you out. People, you know, we talk about oppression cause that's really what I'm getting at. We talk about oppression and how it shows up.  But people don't understand until something sometimes tragic happens to someone, and we referenced this earlier about some of the tragic events happening to black women  and higher education. Oppression can really cause you to have some dark thoughts  and to feel a sense of hopelessness, and I remember being in a in an employment situation where the the oppression was so great. I was experiencing discrimination because I had a disability, and I dared to address it.  The oppression would be so great. I remember going into my office  several days, and I would just cry. I would feel like I was never gonna get out of that place.  and I had to really reach back, and I wasn't always successful. But I tell people, you know, I've learned that things happen for you, not to you. And while that those events did not feel good. It helped me to prepare really, in some ways from where I am right now. It helped me to learn how to forgive when I didn't feel like it.  It helped me to learn how to be creative and navigating the next steps of my trajectory, and these are all things that I learned from my childhood, and how to be resilient and how to have joy while doing it. So yeah.  so at this point we'll take questions from the audience or from our guest on Zoom. If you want to just signal to me, I'll come to you with the microphone.  Thank you, Dr. Kaiser. Dr. Betts is Christina Downey. Hi, friend, you're wonderful. So II have a kind of a practical question, and it I'll share 2 examples to illustrate it. So I'm thinking about languaging. And I have one faculty colleague who  insists on creating Powerpoints for their class that only have images on them, and then they will speak, and they, their kind of position is well. If the students are really paying attention, there shouldn't be any words on the slide, because that will just distract them. And you know they they need to be following what I say and take their notes from that, and just thinking about how to approach that as not being inclusive.  Another example, though that was more hope. Producing I was on a zoom with a number of colleagues who run a particular resource center, and they kept talking about the walk in hours that they wanted to plan, and as I'm listening to this conversation. Eventually, I said, you know, I think that the term drop in hours is the more inclusive one, and they immediately all just switched like instantly switched in terms of their language. And  you know oh, we need to go look at our documents, etc., like they. They took it just fine. So 2 very different examples about how to kind of manage practices and languaging. And I wonder if you can speak to like. Is there a general way. That we can raise these kinds of languaging or practice concerns with our colleagues and open these conversations in a safe way.  Sure. So. I'll start with the the language part first, and then I'll answer the question about the colleague, and this is just from my perspective. And there's other  experts in the room that provide accommodations they may also have something to share. But I'm going to start with language first.  So going back to my comments around, how we have been socially ingrained to think about certain things, or you know, maybe not even connecting that  language has history, that words have history just like in other identities, but because we have not always censored disability, not just, you know, at our school, but at other schools like it's very common for people to not think about language. And so, as we roll out a community of practice that will probably one of the things that we will provide like that. We could upload to our website. It's  some training and some, you know, resources around language in the history, particularly for the disability community. And I think you know just what you did like having a conversation like, Hey.  you know, maybe we should move away from using walk in hours. To drop an hour, you know, having that conversation. And and then people think about it. There's other times, you know, where people use language.  And they're not intending or not thinking, but it can. It can be a microaggression. And so, I think, being willing to have some of those brave conversations a person at a time. And I think, as we are working to frame a culture around a community of practice and having people begin to think about this. After a while we will have to do less educating because people will have the tools.  People will begin to think a little bit differently, but it will take time.  As far as the question around the faculty member. That is wanting to use pictures, I think one, you know, telling the faculty member that you know there are different mo modalities of learning. Not everyone learns in the same way, and not everyone is a visual learner. And then I think the other piece is.  you know, we want to be inclusive, and a part of that is accessibility. And so how can we work together to come up with some other. You know, ways, other modalities of, you know, getting the information on these slides. What could that look like? And I think  in addition to that, and I'm not sure exactly what we do, but I don't wanna misspeak. But I think if there is a way I know sometimes when faculty. New faculty. Come, there is like training that happens over a few weeks of time. And then, you know, if we have some training around inclusive practices. Not just talking about accommodations, but really helping faculty to understand what inclusive  practices are around accessibility. I think some of these things again over time will begin to shift  I, just, I wanted to add, if I, could just with the identities that I hold is to build on Dr. Beth's comments from a scholarly, pro sort of practice and a practice of love  moving from a pedagogy of love is on your first point, I think. When you're in a position  of power as you are when you're teaching a classroom, and you're making pedagogical decisions. When a colleague or a student or someone is trying to provide loving critique  about different perspectives or different ways, different modalities to Dr. Best points, different pedagogical moves, where you're considering the variety of how people learn, but also the modal, the modalities in which they can access information. The first thing I would offer that we do when our colleagues. Our communities take that risk of love and give us critical feedback is to believe them.  I think, to your to your second point, this notion of folks being more reflexive, taking in feedback and quickly translating that  I think, is a sign of deeper excavation of the self  and getting to that point of belief, and then moving into practices that change and shift, and I think, leaning into celebrating those spaces and guarding the spirit as you enter other spaces that are able to set the intersections of other forms of oppression is also necessary. So I just wanted to add that from my perspective, both in scholarship, teaching classes, making pedagogical decisions, and also with the identities that I disclosed earlier. I wanted to lift that up and build on Dr. Betts comments.  So my name is Michael Mace. I'm the manager of the assistive technology and accessibility centers so to weigh in a little bit on the Powerpoint. Powerpoint.  So. not knowing the context of the conversation, the Powerpoints in general. There's a lot that could be dissected there.  Everybody processes information differently. There could be a perspective from that, Professor. If you put too much language, if you put too much information on the screen, then you're confusing 2 channels  of consuming information. If I'm reading, or if I'm saying one thing and the slides are saying another, then you have a channel conflict. That's gonna  really hinder the ability for you to understand the information.  So what we normally do when you have a slide that only has information or only has graphical information on it.  First off we work that instructor. We say. let's say it's a ski. It's a skin cell. That's the one I usually use.  You need to describe that skin cell as if  the person  cannot see the skin cell. So you want to describe that the top layers. I am not a biology person.  the top. So this this top layer is the epidermis underneath. This is the fat layer again, not a biology person. And then underneath that you have these squiggly things, and you know, go on, and you want to describe it any. Sometimes, you know you want to use positional language. So I already screwed up right? I said. The top in the middle and the bottom. You just kinda wanna describe it  as you would how you would feel it, or how you would interpret it.  As if you were dissecting it right, try to do it, and and also try to do it in the best way you can, understanding that you may make mistakes cause  you're human.  We also also have something called all text right? So if you're going to hand that Powerpoint out.  then the instructor needs to describe what's in there, and they need to put it in the alt text. Or, better yet, what we would ask is, make that a word document, because Powerpoints.  horrible to navigate with a screen, reader. cause you navigate it most of the time  in creation, mode not in consumption mode. So you get to hear lots of positional information  like the images at  this point. Pla, at this point, point, this point, I mean, Mary could talk a little bit more about it than I can.  and she's laughing. So you know, there's lots of nuances there. We're always happy to talk to a faculty member about the nuances of creating accessible materials.  But yeah, it's all. It all depends on what they're trying to do.  But they should have, you know, they definitely need to describe it in class. That's the whole point. And honestly, they need to describe it for everyone, because how hard is it for you to write notes, look up, look down, listen, mean it's beneficial for everybody. If you're describing what's on the screen.  right? If you're describing the skin cell as 3 layers.  and in that 3 layers there is a there's a layer on top. There's a layer in the middle and the layer on the bottom.  Well, I hope I'm doing this. Okay, Mary. Yell me later. but II just wanted to chime in in there, because sometimes we can. we can. and trying to accommodate, we can almost  do the wrong thing. So we want to just be cognizant of of how we're trying it. And if you get, if you have questions, you can always reach out to us, Atac at Iu. Edu.  I just have a question. Hi, I'm a Q. I  was wondering. Since we're talking about the different ways that faculty, can, you know, reach the broader audience? What is there some sort of ongoing training, or is there some sort of  check in that? They have to do just to ensure? Or is there some something going out to them to ensure that they are being inclusive?  I'm gonna refer to my Aes colleague in the morning.  Yeah. So there's no required training.  And the person I would refer to left the room.  but we do have a voluntary. We have 3 training classes. They're out on expand  expand. Iu Edu, that is the university's noncredit education portal. And so there are 3 courses. You can take. The first one is Ada awareness for faculty.  but highly engaged, that you have your faculty. Members. Take that one.  Right? So that's the first one. The second one is, help me out, Sarah. 7 simple steps.  So the 7 simple steps are the basics of accessibility. This is all text. It's headings. It's close caption, your videos. It's all that fun stuff. It's easy stuff. It's the low hanging fruit. It's the stuff you should do before you call my office to help you out  and then the third one is increasing the accessibility of your canvas course. So those 3 are, gonna get you in pretty good shape for proactive accessibility.  And then at a certain point, you're never gonna be. You're never gonna have the perfect accessible course.  But you can get close, and then you can call us, and then we can work with the accommodation  integration for us on the twenty-fifth and one of our sessions so that we can begin to learn right? So it's not about what do we want to do in response to what we're learning? And how much of  how much are we willing to change and to grow? We're one in university. And it's all about education, right? So community of practice is all about education, but the individual person has to want to be educated and also share what they know with others. So that's how we become a community of practice. Very informed. Thank you.  Don't miss that session.  II just I just want to. As I set up a as we pepper the I want to honor the zoom space, too, and I'll be queued if there's any zoom questions. And as we get more conversations in the room I want to pepper back and forth with this fireside chat, and I want to push us.  I want to push the conversation and then then I'm gonna put it all on, Dr. Betts to answer. yes. so  for me as I'm as I'm making a commitment to arrive at solidarity, at the intersections of things that impact me.  and I've experienced oppression at the intersections of things that don't impact me.  So my experiences with Ableism are as a perpetrator of harm.  My experiences in the Academy teaching and learning is as a per a perpetrator of harm. And so I know, then, that I have to move. I have to include things like alt text and screen readers and technical ways that I make a learning environment more accessible.  But I also have to understand that I have to interrogate my own value, set my own ideologies the way I consume who and how I show up for what causes, what other causes are not on my  radar and so how am I thinking about as I, you alum? Alice Wong encourages us to make disability a visibility to make it more perceivable to acknowledge that people matter with disabilities, that how they learn matter.  So, as I'm crafting a lesson, as I am receiving feedback from colleagues, I have to understand what Dr. Betts that she was gonna circle back to. And I want to circle back to now. It's this word of complicit  in harm. Dr. Betts.  Okay, complicit and harm. I think that.  you know a lot of us in the room. We know these words. We talk about these and social justice work  and I think you know, when I when I kinda called us into the work, part of it, is pushing back against complicity and and either doing something or speaking up  when you see harm, and that may come at a cross  and you know II talk about in my office all the time. I talk about Betina love being a co-conspirator  and you know, we talk about being an ally in a disability community. But we need co-conspirators. Recognizing that, you know, we sit in certain seats.  And we have a certain level of power. And so we have the ability to not only, you know, bring the concerns to the table, but bring these groups to the table. But sometimes things are not gonna be popular. We may only have a certain amount of money for certain mean certain priorities, and we have to make hard decisions, or we may only, you know, there there may be things that are not popular. So I'm gonna give an example about  kind of being a co-conspirator and and pushing the work for that. III took at an institution as a person who had a disability, but was not necessarily in some of these rooms. So  we were working on a diversity action plan. And there have been much conversation between the disability community on this campus  and the the diversity leaders around, like we don't see ourselves reflected.  And this work, you know what is going to happen. How can we be included in this next plan? And the the leaders of this plan were being very intentional. They were working with constituent groups. They were getting well respected leaders from these groups  to give voice to different outcomes on this plan, but there was no one in the room to represent people with disabilities, so I was low on the totem pole as far as Staff, so I wasn't in the room at all. But they were talking to some of my student leaders, and so  I happened to run into one of the students. I was like, hey? How's the meeting going? You know. How is like, what's you know? Like, are they talking about this? Oh, no, they're not talking about disability at all Miss met.  I was like, Okay, so I connected with our Ada Coordinator.  And I said, Hey, you know, like there's some serious conversations happening about the design of our next student, our next diversity plan. And we've been talking to administration about our voices not being included in the space.  And he's like, I tell you what, let's let's get members of the disability community together, because I can't write the letter, but you all can.  So we wrote a letter to the president of the University. I did this as a staff member, which meant I could have maybe probably have been fired, but I knew that the need to have disability and the climate issues that we're facing addressed  on our campus at that time. It was worth it to me.  It was worth it to me and many others. So we wrote a letter to the President, you know, around the it was the 20 fifth anniversary of the Ada, and we lifted up. You know, this is a a historic year. We want to use this year to elevate disability. We wanna talk about. You know, we wanna address some climate and culture issues. He was very supportive. It never made it to him before, because, you know, in politics, higher education, there's gatekeepers.  And so we were able to bypass the gatekeepers, and he supported a year long initiative that would have never happened if I had just, you know, acted like. I didn't have the knowledge that I had and not said anything.  And so the call, you know, the cost was, I probably made some people in my division mad? Did I care? No  because at the time it kinda was what it was, but it it paid a foundation for improving the climate of people to come behind me, and people during the time that I was there who are part of the disability community. And so sometimes, when it comes to pushing back on institutions and systems. And I understand that we, we have families, we have things that we have to weigh and we have to consider. But sometimes doing this work  doing this work comes at a cost, and then the oppression that people experience when people are unwilling to, when when people are continuing to be complicit or not stopping the harm it also costs.  So that's that's what I have to say about that.  Any other questions from the audience. virtual or in person.  Hello! My name is Emily Munson, and I'm adjunct faculty at the law school.  I was wondering what your help?  II would say, what are the  top priorities? Top tab 2 priorities  for improving students ability to  get accommodations.  on campus. I know that  from the agent faculty side. Students have told me, like  note takers are not being paid anymore  for taking notes. And so  students  but they also have to arrange  your accommodations individually with each professor.  are there any efforts or priorities underway to  streamline the process, to take  some of the burden of getting the accommodations arranged off of the individual student.  So I'm going to refer to Doctor Cannon.  So I'm I'm going to speak between  what I know as an associate director, and then what I know as the director, as an associate director. I remember that we did have note takers. That  partner we partner with  the law school to make sure that the students had notetakers.  And it was a a  a system that we had in place for quite some time that was not working out  as smoothly as it was, will stop working out as smoothly as it initially was working out.  And so we ended up working with Atac and Assistive technology accessibility center and implementing a software where students could use a notetaker. Electronically.  it's called gleam Philip  And therefore, under  Dr. Mccracken's administration, I believe the shift took place to students being able to just  use that right.  But it wasn't a decision that Aes made. It was a decision made between  the law school and a yes, about in person. Note takers that had a lot of nuance to that.  We can always revisit that conversation to find out exactly What you're asking, Emily. And if there's a preference to have the in person they'll take taking system again. What would that look like? And how would that not violate? Some of the  technical standards that the law school may have in place, which might have been a big  reason for making this shift  so we will have to dig into into finding that out, and I'm open to do to Dornet, so could we like talk later, set up an appointment and have that conversation.  Emily, did you hear me?  Thank you, doctor. But Amy Warner first of all welcome to. Are you Indianapolis? Thank you. Dr. Cannon. Thank you for coming back.  And, Dr. Kaiser, we are thrilled that you're in your new position  and very proud of you as an alum of our campus. So thank you all. What powerful women  with today's discussion!  One of the questions that I had sort of struck me, Dr. Betts, as you were sharing about your mother's journey.  and the responsibility that we have as an employer  to also bring undergraduates and graduate students into the work world as part of their experience here. And I'm just curious if you've seen models like that work. If you have some suggestions, or if there's a way that we can begin from the beginning creating a great work environment so that students are leaving with their degree.  but are also leaving with experience that permits them to be employed  after graduation.  Sure, this is a wonderful question, and thank you for asking, because this is an important part of the student. Experience is to to work as an undergraduate and to learn all of these transformable skills.  And so I have a couple of thoughts. So first of all, there, there is a program.  at a Columbus, Ohio, under a nonprofit called right choice. And it is an internship program for people with disabilities.  The program focuses actually on students of color with disabilities. And the program  works with companies all over the city to place students, and then they provide kind of like a cohort, model mentorship and address different things that may come up in the workplace.  and it is. It has been in operation for about at least 12 to 13 years. It has great success.  I think that there is an opportunity to create  a program similar, you know, because you know, one of the things that we do well in universities is we create pipeline. We we create these mentoring pathways, cohorts where we can, you know, kind of talk about what people experiencing on their job site work with different work through different scenarios and questions, with not with the student employers, but also it gives us the opportunity to do some coaching  around culture and climate issues for our different departments who may not have had a person with a disability work there. So I think there's lots of different opportunities that we could  think through  and I think there, that we have a lot of lot of to to create something unique that would work for our institution, and that would benefit lots of people, and II think that it is a worthwhile endeavor to to consider. So thank you for bringing that up.  I think we have time for one more question before we, before I turn it over. Before Dr. Beth and I excuse ourselves, and I turn it over to Dr. Cannon. You have some thank yous, and then I'll close out as a mistress of ceremonies  our opening celebrations. So we have time for one more question. Wanna honor again. The zoom space  as well as the physical space.  Give some more thing time. If not, I've got one for you, doctor, that close us out.  So I'm thinking a lot, Dr. Betts, about this idea of moving beyond awareness to circle back to our theme and moving into full inclusion  of disability, and I should offer advancing disability justice on campus  before I ask this question, I just wanted to phrase where I am at my journey is understanding, as I've learned from Dr. Kathleen, King Dorius. This notion of paradigm, shifting from deficit views of persons with disabilities to asset views, but also shifting from placing the onus and labor on people experiencing harm. And this in this case versus with disabilities on to the systems that are re-fying that harm.  and one move that's been helpful for me. Doctor Bets is that it's in the frame of disability justice for me. This isn't to take away the claim, and the name of disability, but a shift in a paradigm, and hopefully a shift in practice is that it's not persons that are navigating educational spaces that are disabled. Rather, it's educational environments that are disabling. That's right.  And so my question is, can you give us some examples  of realizing full inclusion of persons with disabilities on campus.  Wow! This is a great question. So  so yes. So II want to. First of all, I want to give an example of my own experience of times that I have had to navigate  educational systems as a student, that we're disabling.  So when I was in graduate student graduate school, my first time going into graduate school. I showed up to graduate school. And because I had had access to the adaptive technology that I was used to which is called Job Job access for windows.  This was years ago. In the early 2,000.  I assume that it was going to be there at the graduate school. So I get there. I'm excited  and I go to get my laptop. And I'm like, Hey, you know  they're like, Oh, we don't. We don't use jaws we use. I forget what they were using at the time, but it did not  work well, and I was just like, Oh, my goodness! And you're like, well, you know, we we don't really, you know, we're not gonna really get that. There's not too many more people who use it. And so I was like, Oh, my, gosh, what am I gonna do like? I just moved here. I really need to be able to have jobs like, how am I gonna do my assignment?  And so this is in the early days of where they had compliance offices, and I happened to meet the compliance officer when I worked at Vincent's University I brought her to do a title 9 training. This is way back in the day before they were coming place.  And so, you know, when I came to the school she was like, whatever you need let me know. And I was like, hey? You know, I need jaws.  I need. I need to be able to have access to jaws in my office as well as  for school, because you know the the system that they're talking about, it doesn't really work well with a lot of other things just like, Oh, you want jobs. No problem. We're gonna make sure you get jobs. And she had that she purchased it for the office and for my assistant ship.  And so there's a very, you know, short amount of time, or waiting for it to be purchased, and all that kind of stuff. But just that moment was terrifying. Cause I you know, I was like, well, what am I gonna do? This is before we had lots of different models of adaptive technology that you know, kind of. Come on computers, we can kind of make it by. This was, you know, like, if you don't have this, or I think maybe one of the ones back. Then was window eyes.  This was back in 2,006, but just that moment was terrifying, like I definitely felt  handicapped. And I don't like to use that word, but I did not have what I needed, for you know a couple to to make it in, and after I had, you know, made a major move to go to graduate school. And so, having people understand  in that moment, like why, it's important to have a couple of different types of technology. And this particular technology that I'm talking about is very common. And it worked well with lots of different  systems like the Internet and outlook and things like that. Instead of having to prove a case.  having to prove that I needed what I needed. You know, while time was kind of going by with classes and my graduate assistant ship. So the ideal situation would have been to, you know, not only have jobs on the computer that was checking out, but at that time be able to download it from anywhere and to use it. And we have some systems set up like that here. But that is the adaptive technology, but also the culture and the climate. So sometimes we focus on  the accessibility piece, the Ada compliance piece around the accommodation. But you can have the wheelchair ramp. You can have the technology. But if you have a cold climate towards disability, you still have major problems. And so that is sometimes where  some of our work needs to be. So in order to kind of show up authentically and feel included. I think we have to. You know, we're coming up with these culture climate surveys. We have to assess what the institution needs to learn, and we have to assess from the community what their experiences are. So I think, you know, working to improve campus climate explicitly  seeing representations of disability throughout the institution. So when I think about, you know being able to critical mass. So we talk about a pipeline in in research around communities of color and the importance of having a pipeline because they create mentorship for undergraduate students. You know so many benefits. But we don't have enough people in higher education that have faculty or professional jobs  in that have disabilities to sometimes create a critical pipeline. But you know, seeing language that you know explicitly affirms disability, or that acknowledges it in university plans. These are all things that speak to wanting to create a climate that is inclusive and create spaces where people can show up authentically in all of their identities. And so I've named a few things. But you know the climate, the the actual accommodation piece  and then I think a philosophy kind of like what we're introducing as a community of practice here at Iui.  Dr. Betts, on behalf of the virtual space and the physical space. I want to thank you for warming us with your passion and encouraging us, and I know for me, soothing us and and giving us encouragement by the light of your moon. I am indebted and grateful for you to share space with us today. I'm honored to be able to engage in this fireside chat with you today I look forward.  Engaging and more learning with all of you in this space, in the virtual space on this campus broadly, and of course, in the university system, with the positions that I hold both professionally and personally. Please join me in thanking Dr. Bats for this terrific fireside chat. Thank you, Dr. Bats, thank you. Thank you. Everybody.  I now want to move us to a close, and, Dr. Canon, I want to turn it over to you with some. Thank yous, unless you want me to handle those before.  Okay.  okay, thank you. Okay.  alright, thank you? So I want to recognize The student organization leadership advocacy group  Mckinney disability wanna recognize those folks. Thank you to our external tabling guests. This is also in the middle panel of the brochure.  If you wanted to perceive that as I'm going through the thank yous  want to thank all the students, faculty and staff and alumni on and off campus  that will that are here and present virtually or physically, but also that will participate throughout the myriad of really intentional, thoughtful, and what I think will be powerful experiences through the through the month of march  and to acknowledge the community of partners that are here different government. And you municipal sort of presence that are here. If you're here from the community or representing governmental entities or government offices, if you wouldn't mind showing that you're here by either rising or in in whatever way you want to to signal to us if you're here.  Well, thank you. II see some folks thank you for being here.  Thank you so much  in closing and I would offer if we wanted to. For those that are interested. I think, just as mia mingas encourages us to leave evidence  that we were here today. For a group photo. If anyone's inclined to stay around for that, I would offer leaving evidence of today is important but in closing a short survey there's a QR code again in the middle of your brochure. For those in the zoom space. My assumption is you'll get some sort of follow up with those in person  email as well the accessible education services is a is a organization of continuous improvement. They want to understand what went well for today, what can be improved. And so I'm sure taking 5 to 7 min to complete that survey.  That would be something they would be really grateful for. The QR code is now on the screen, too. If you have an electronic device and would like to capture the QR code as well. So with that. Thank you all for a wonderful lunch.  Please enjoy the events for the remainder of the month, and should you be so inclined for a quick group photo feel free to navigate to the front of the room, and again, please join me in thanking Dr. Dace Dr. Betts and Dr. Cannon and the Aes staff. Thank you so much.

Zoom Recording of Luncheon Event (transcripted audio only)

Mistress of Cermonies:
Dr. Tiffany KyserDirector of Outreach and Engagement for the Indiana University Alumni Association

Presenters:
Dr. Karen Dace, Vice Chancellor for Diversity Equity and Inclusion
Dr. Mercedes Cannon, Director of Accessible Educational Services
Speaker:
Dr. Katherine Betts, Assistant Vice Chancellor for Diversity, Equity, and Inclusion

Just saying that you can be here, or that you can have the accommodations to be here, that is not enough. That is the floor, not the ceiling of the work. We want people to feel included, and to be able to show up authentically as our full selves. That is what we want for every person at IUI. – Dr. Katherine Betts.

IU Indianapolis Nina Scholar's Program Panel

Intent: The intent of the Nina Scholar’s Panel was to allow for current Nina students and alumni from the program, to share their lived experiences as a disabled student at IU Indianapolis and to learn about their experience as a Nina Scholar.

Impact: This panel shared their experiences as a disabled student on the IU Indianapolis campus, feedback for IU instructors regarding supporting disabled students, and how the Nina Scholar’s program has supported their academic journey and helped establish a sense of community.

Description of the video:

 Another scholars program started in in 2,001 funded by the ninety-minute employee and charitable trust.  So we've had just at Iu pui. We've had 206 scholars in that time, and I've been here for almost all of it. So I know all these students say maybe one, since since 2,001 this is so 20 years for me doing this work, and 29 years in higher education the previous time was mostly on the graduate level.  so now I already mentioned sort of so who are who our students are? But I can add that so we we were just the Nina Scholars program for quite some time, and then in 2,014, I started talking to the Bowen family foundation about the power of programming connected to scholarships and support connected to scholarships and curriculum connected to scholarships. And so they started the  own scholars program at Ib tech like, oh, 9, 2010, something like that. And then here at Iui in 2,014. And then I was talking to the Vice President that 9 Mason, fully internal for us about people would tell me that 9 of scholars couldn't be scaled. It's too expensive per student.  And I said, Well, let's focus on  the elements that are scalable, like the community, like the culture, like the curriculum, like the engagement  and that thrive was born from that conversation, and so thrive now is is in its seventh year, and it's just been funded for 5 more years.  In 2018 29 scholars was in doubt.  so we trust, gave us a significant amount of money that the University Foundation could invest.  so that none of scholars can exist in perpetuity. So as long as there's a now iui. There will be a 9 scholars.  Oh.  now we're trying to figure we've got more that we need to spend. That's a good problem to have. Right?  So I said, $206 since 2,001, our graduation rate. During that time is 78, which is higher than we're talking about. Students from lower income backgrounds, from meeting the significant challenges in life. And you know, students  like, I said, you know, experience a lot of not just challenge. But trauma  complex. Really thinking about it. And these in our graduation rate is higher than universities average over that period.  Our students take our significant graduate school. Our funds are very community involved folks often leaders in the community.  And our students take 2 semester courses which you kind of. As you sort of alluded to, our students take a course in  basically self discovery and empowerment in the first semester and the second semester of my face. Emotional intelligence.  and that's really what I wanted to tell you about kind of our programs. Now, what I want to do is have our panelists introduce themselves, and what start? Let's should be with us virtually, and then move on to Lance Matt. And really, what I'm  like for you to do is just who are you number one, and you can include you know, Lance as a current student, and next to Dr. Alums, but some, some, maybe some academic information. Whatever you want to include about career, perhaps.  and then maybe maybe just a sentence because we'll have lots of questions that will dig into other elements here. But why this? Why? Why disability? Awareness? Month is important to you, or why this topic? Why, this work is important. Okay, does sound good. shadiyah jones: Aye, stop, please. shadiyah jones: Okay. So my name is Judy Jones. I am a scholars. Alumni and currently I am live coaching. That's what I do. I really enjoy that. It's very fulfilling and meaningful for me. And I feel like the disability awareness month is very important, due to the fact that we can bring awareness to disabilities, and also allowing people to see as regular people. Although we have a disability, we still want to do regular things and live our life like regular people. So I think that's what is very important about this ability. Not for me. And in my opinion. shadiyah jones: anything else, Charlie, did I cover it got it. Thank you, Judea. Lance.  My name is Lance Barnell. I'm a scholar. My junior year. Also, was part of the program at Ivch, which was a great experience. I am  in the O'neal school, public environmental affairs, pursuing degree in sustainable practice and policy. I'm very  passionate about environmental issues and and issues that concern sustainability.  And  you know, this this month is is important to me. Because, yeah, I lost my sight 8 years ago, and it kind of thrust me into a community.  And with all the interesting and and positive things that go along with that, and and so.  instead of of being resistant to things like that, I'm embracing that and it. It makes me feel good to to represent.  You know, the blindest community today.  Yeah.  I'm Matt Griffin. I am a nice scholar. Alumni from 2,009 to 2,012  so it's been a it's it's always nice to come back on the campus and see everyone that I recognize and even basis. But really being here on the panel today for disability awareness month  to me, what's really the most important is just normalizing disabilities. There's a lot of people that think that your life ends. You get a disability, or you're born with a disability. And I could say, from personal experience, I've lended insanely fulfilling life more fulfilling than honestly a lot of people probably feel that like this will, I exposed early to adapt  playing in a our wheelchair. I fortunately lost a lot of weight and tons of physical therapy management there now, and can't even walk a little bit here. But really just normalizing disabilities. There's things as simple as ramps in home, so we're in wheelchairs. Can't come visit you  I just recently purchased a new home, and the first thing I did was put a ramp in, even though I couldn't manage to get up step or 2 to get into the house. I have many friends who cannot. So that was the most important thing to me. So I have friends who, you know, visit me and  see the house that I've been fortunate enough purchasing.  really, just making sure everyone understands, even though you have disability, your life can be perfectly normal and exceptional. Whatever you really put your mind to.  One thing I did forget to mention. I did go to technology.  Thank you, Matt, and then I'll I'll let me say real quick before we start jumping to our questions. That. You know, this work for me is a calling and that's partly because I've experienced any of these things that I come from an independent youth background. Personally low income personary to college.  lots of trauma, and included in that is, I had a traffic brain injury as a kid from a near drowning accident.  And  the thing that I'll echo that I'm sort of hearing is is the journey that we go on?  I mean, I'm still on it, of course, but it's it's a heck of a journey. It's it's a healing journey. It's an acceptance journey. It's a post traumatic growth journey. I think in some way I don't know if everybody feel feel that or see it the same way. But but I could say, that's certainly  through in my experience.  Alright. So let's dive into some questions, and I think, at least for this first question, release to go in the same order. We just ended. Well, we may mix it up later, but so should he will start with you. But the question is  personally reflecting on your journey as an undergraduate. What advice would you offer to your high school self? Okay to your high school self regarding navigating college and academic life with the disability? shadiyah jones: Hmm, advice. Yeah. shadiyah jones: I think the advice I want to tell myself is that you're not gonna be alone on the journey. Because when I was in high school. I was the only one that necessarily well, that I saw with a disability. So I did not see many people who looked like me, or was in a situation like myself, or really even had a disability at all. So I think I would've just told myself that you will not be on this journey alone, and you can go on the journey and feel confident to know that other people around you shadiyah jones: can understand what you're going through shadiyah jones: fun. Thank you, Shadia.  My high school self was that was a long time ago, but you know, and and I had 2020 vision.  But you know I would tell my high school self.  You know there's gonna be some things in your life that  no, we're not gonna make some changes for you. And I think  I was probably pre resistant over the course of most of my life to  You know more of, the idea of community and and interdependence. And you know,  leaning on others, and  you know, but like-mindedness and you know, if I had embraced that thought  long, long ago, I, you know it would have better prepared me for for my life today, and you know, as person attendee, you know  But  some of these things you. You just can't. You can't learn them until until they they are in front of you, and you're walking through it. Yeah. So I would have told my high school self these things so my high school self probably wouldn't listen. Good point!  There's a ton of advice. I wish you could give my high school self the fact that my high school self would not do it. That is spot on 100. I never even thought about that. Every 100.  I think.  reflecting again, it's it's been a bit for me since my high school self, but  having the confidence, believe in your abilities is really what it comes down to.  Ow!  All the way through elementary school I struggled with confidence, always thought I was stupid. I always thought I couldn't do things  very detrimental thoughts to myself.  and as I've grown older and matured, I've realized that there are struggles that everyone has. Mine are going to be different than yours. Words are going to be different than the person next to you.  but really just having that confidence to say. I know I can do this if I don't know how to do this, I can figure this out. and you know  I don't know right now. False confidence is not a good thing. Having confidence is a good thing.  There's tons of other things I would love to  make sure my younger self. Do I luckily have been involved in the adaptive sports community college, but really kind of driving home. That point to my high school self community is one of the most critical things community is going to set you up for success the rest of your life.  and I'm sure they still beat this into everyone's brain as a student. But networking is critical. That is where community comes into play, and being involved with some kind of community is a type of networking getting to know people, having conversations that's going to help you have the most success you can post graduation.  III have to add that that was a natural champion.  Alright for this round. Let's whoever wants to answer first, go for it. As a Nina scholar.  How at this scholarship program contributing to your academic journey supported any barriers, to how many barriers you face the higher education, and how have utilized the knowledge gained as a Nina scholar in your work for the loans outside of Iui, and and latest, you know  presently. How is it going? Who wants to go first?  I can go ahead and start if everyone wants to think on that one  the thing that stuck with me the most of the time. Scholars. I really came into it, not knowing what to expect. It was actually my second year and Ipoi when I joined the Mountain Scholars program  and I was really amazed in the  well, I'm gonna say, retrospect force community inside out program we actually had a class with inside out and getting exposed to  all of these different backgrounds. Like, II already been exposed to a lot of people's backgrounds just from the adaptive sports community. A lot of it was all physical disabilities. It wasn't really any involvement with people with visual appearance. Intellectual impairments, things like that. And really a lot of the  a lot of the programs at 90. So as we do is just more cultures understanding and reflecting on people's differences.  What makes them have stronger abilities in some areas where I was weaker and really driving that community. And that's something that, even after graduating, I still heavily reflect on that.  and recently married. And I have to remind my wife frequently about like we are very fortunate like we're living.  and she's a nurse. So she works around doctors who very well be, and it's like we're not doing as bad as it might feel like, based on the people you're currently exposed to  get yourself involved with. People who are less fortunate understand really what life is like outside of the bubbling area. Because when you're around surgeons all day making half 1 million dollars a year, it's like, Oh, our Bros could be, you know you're not. You're nowhere near broch and it it's just fascinating. And having been exposed to that, and continually reminding myself about how fortunate I am about where I've got myself.  because I also came from a very impoverished background. Single mother who raised before I was in college. So it it's it really is a journey, and it might at times feel like you're never going to get out of it.  But if you stay persistent and gain.  so  I mean, there's a lot of things I could say about the specifics of what I gained from the program, you know, because there were a lot of uncertainties. Starting. I  had been to high school since 1985, you know. Starting an Ivf, I just I didn't know what it was going to take.  And during my second semester, you know contact, and I'd be texting. You know, there's this program upstairs. But really.  okay, that sounds interesting. Let's go up there right now.  you know. And oh, they've got a tutor. And there's this thing called blind finite math coming up that you have to take. Let me tell you something about blind, finite math. So you know this, there was a tutor who has become a great friend.  and we work through that together. There's a way. But and and you know so the the specifics of the program  and the tutoring and and all that stuff is significant. But what I found is is  the days I'm just at home doing this work on my own.  knowing that I'm a part of this.  and and knowing that I'm a part of this community of this group of scholars.  There's something about that that helps to keep keep one going. and to to know that  it's not that I have to ask Charlie  Format or anybody. And it's not that I'm I'm looking to add some for everything specific on any given day. If I need to do up good  and just having that in mind, and knowing that it it has meant a lot to me.  It's  we can put a price plan.  That's that's what the program's meant to be. shadiyah jones: Do you want to add anything? shadiyah jones: So yeah, of course. So academically, I feel like the 9 scholarships help to my academic journey. Just do shadiyah jones: to the support that I had, and but I feel like I still have, as far as with being able to talk to Charlie and call on him, if you need any help. And just the people that I've met, that a lot of the friends, and like the family I feel like has been created, has been so supportive because going into college when I was around like 21 shadiyah jones: didn't really feel like I wanted to go to college. I was just bored with life because I got paralyzed at 16 and ended up graduating with advice. But I was like, Well, what am I gonna do in my life? And I was like, well. shadiyah jones: I just go to college. So I was like, I went. I got accepted, and I was like, well, now, what am I gonna do so. I was just kinda rolling around, not really knowing what I wanted to do. But then I met somebody who introduced me to the Niners college program. And I was like, Okay, well, join this. And I joined. And it was nice cause again. It was just that support and feeling like you could achieve the goals you wanted to reach as far as academically. So shadiyah jones: so that's how I feel like it's been supported in that area as far as the barriers that I face with higher education. The one barrier I will said that I did face was just not believing in me, and I had Charlie, and he was able to talk me through. It was like should be because I started off taking part time classes. He was like. Would you like to move to full time. and I'm like, no, I don't think I can do that now. I'm okay. He was like, I think you can. shadiyah jones: So that's what really kind of gave me that push to go full time, and shadiyah jones: crazily I was able to do full time, and II did it and graduated. So it's been very helpful for me in that aspect and just in life today, because of the skills and the things we're able to learn with Charlie just about mindfulness all of that stuff. I still utilize that to this day, and it has really helped me excel in my adulthood, and just in my the challenges that I face with my disability and life every day.  Yeah. So you know, some of the one of the things we're hearing is this internalizing these negative messages about our work. Capability and general is sort of unpack that, and go on this little learning and growing journey of really understanding ourselves. And part of that is really you know, figuring out what to do with that those inner critic kinds of voices that say we can't  understanding how that all works, even from a, you know, from a neuroscience perspective. How does it all work? And then what are the practices that we can use and develop to to navigate all that with compassion, with self compassion, especially and then Matt mentioned inside out. So I'll say just a teeny bit more about that. It's been a while. But we used to. I'm certified to teach in in incarcerated environment environments where people are incarcerated  and re-entry  situations. And so we would. We used to take half of our students, or we, our students, made up half of the class, and then folks from an incarcerated background would make up the other half of the class. So we would learn about live transitions like, how do you make but our live transition? And how do you make successful transitions like  that was part of that? That. We haven't done so.  Alright. Third question start with, whoever wants to wants to be in with your identity in my.  how was being an undergraduate, disabled student shaped your experience within our university?  So again, with your identity in line, how was your undergraduate, disabled students. Your identity as an undergraduate, disabled student shaped your experience in the university community.  Let's start off. shadiyah jones: I can go. shadiyah jones: I feel like my experience. IUPU. I. shadiyah jones: It should I mean for who I am today? Honestly, II can say that when I at first came to IP. Why, I was probably fresh into about 5 years of being paralyzed, which is still very early, so I was still at a place of trying to accept my situation, and probably still a bitter about my situation, because it was very difficult to deal with, and I just didn't feel like I could fit in with everybody else. So coming to Iupy again, and just having that support. shadiyah jones: and being in the Nina scholars having the support of the people that are in the group and having the support of Charlie and just the friends and people that you meet. It's just shaped me simply because I feel like I am who I am today, literally because of Nino scholars, and literally because of going to Iupi and being able to encounter the people that have I have encountered.  Thank you. Dia never lens.  I  you know, coming here and starting school  this part of my life.  I mean  the 48 year decided person, and then  you're kind of thrust in it. It does make you question.  You're all out.  you know, even though deep down, I knew  so the  parts of me that really meant something. Were there always going to be there and believe  didn't touch those.  even knowing that I had to go and make sure that that was true. And coming to school was that process  being accepted into the night  scholars program was that process. And there's there's a lot of things  coming to Charlie's class, those  I look forward to that  because it was  a time of day  to take a breath, but he told us something that stuck with. He told me a lot of things that stuck with me. But the thing one of the things I'm thinking about right now was  that many of us believe in this is whether you have a disability or not, that there's something you're missing, and there's a reason why we can't do anything, something that people do.  or why we can't get to a certain level. so  told us over and over again. You're not missing anything. person, and you have everything you need.  and sometimes  you just have to have you just. I needed to hear that somebody would call voice because it worked.  you know, I mean, do I still doubt myself from time to time.  Sure. it's daunting. It's tough.  but there's always a way. When you hear something like that you've got everything you need.  And this is an experience.  I believe  that's  if if that answers the question. I mean, I hope it does. But it's  you know my my identity hasn't changed. Just looks different.  Thanks, ladies.  so I think the  and that sticks out to me. The new house  is when I went. When I came to Ipi. I really, I said, I previously been involved in adaptive community for adoption sports.  I really in my mind, have myself in a box. I was an individual with a physical disability. My friends all have physical disabilities. Oh, do you know so and so?  No, I don't know. I don't know everyone in wheelchairs now, odds are I might know them. But  oh.  I made friends with people, with many, many backgrounds.  people who have disabilities other than mine. Some intellectual people from different cultures, different religions.  and I made great lifelong friends with them.  and I am still friends with them to this day. What is it? 1213 years after graduating.  And I think that's really biggest part of the journey. There was a lot that came with being a college student over those 4 year 4 and a half issues  but really what it it all really does, being involved in the program, it helps you  take yourself out of that mental box.  Make sure you're not confining yourself  to what you think you are. So I  I guess that's really the biggest lesson I learned throughout my time.  Wonderful! Alright. So one more kind of set question, and I've got some more in case depending on how things go. Then we want to kind of open it up to. You. See what your questions are for the for the panel as well. Looking back at your collegiate experiences, what would you share  faculty and staff here about engaging with the disability community to implement accommodations that help foster a sense of a lot. So what would you? What would you? You know, what would you share with faculty and staff about engaging with disability?  Especially as it relates to accommodations. As well  have a lot to say about that I can dive in and start rambling while everyone else go for it. Man  so this was actually interesting, because before the school. So I actually dated by some real staff of the school  when it came to physical disability. It's interacted with all of those items.  But really.  the thing that sticks my mind immediately. Everyone loves icebreakers.  Do you have any idea how many icebreakers are not inclusive like? If you want to have an icebreaker, you better make sure that that thing can be included for people who are blind people who are dead, people who are mute people who have physical disabilities. Otherwise all you've done is stereotype me and exclude me.  I would rather just sit and introduce myself and say, Hey, this is my name. Don't make me do an icebreaker that is physically demanding or impossible.  That's a big one. But amusement plan should be in. Yeah, sure, if I fully understand the question, it's fun to me a little bit more, Charlie.  Yeah. So what what would you share with faculty or staff about accommodation, or just belonging for students with disabilities? shadiyah jones: Man, I probably would have had a lot of ideas when I was at Iup. Why, but now that I'm no longer there, I had to think, but I would honestly shadiyah jones: love to see. shadiyah jones: And maybe this they're not just wasn't included, but maybe more groups, just like support groups around people surrounding my particular disability, because, being paralyzed from the neck down and actually being a paraplegic. shadiyah jones: they're very different. The independent levels are very different, and the struggles on a day to day basis are very different. So I would love to see more people who are dealing with injuries from the neck down that way we can shadiyah jones: to have them feel more included, and not alone, because, honestly, when you deal with the internal like mine, it's easy to feel very isolated and alone, because you don't see many people like you like, as far as I think it's Matt is his name, please, paralyzed from the neck down. Not that I'm saying the situation is easy, but it's just like he has a lot more independence than I do. And so it could just become difficult when you don't feel like you have people around you who are very similar to you, and just being paralyzed from the neck down. So it will be nice if we can just see more people and possibly groups that can include us. And we can have conversations to just know that we are around. And we are trying to be active in the world and bring more awareness to our situation. So we can be considered people with disability. But people are also capable as well.  Yeah, because it doesn't mean our disability holds us back. shadiyah jones: Does that make sense? shadiyah jones: Yeah, absolutely. It does. Yeah, okay, yeah.  yeah.  I would say, if there were  just one or 2 things I would say to the faculty and staff, I  you know, don't ever forget to ask us what we need.  you know.  you know, and and meaning, you know because what Matt, what Matt needs, what Matt needs? Is it going to be on most days? Probably what I need to do.  you know, and II  you know it can be. A conversation doesn't always have to be a solution. Let's just talk about it.  Let's start.  you know, and if if we're not there yet.  we can just say that. you know, that's okay.  But what I would say, you know, whoever's listening to a larger audience does include students or anybody on this campus at all. because I have a just just because I have a disability doesn't mean I don't know how to communicate.  But the thing is, I'm blind. I don't know you're there taking a course. I have taken courses where most of the semester  nobody said anything to me in the classroom. Maybe they didn't say anything to anybody else, either. I don't know, but there's been times, you know, where I stand in front of the class, and you know, like  is so and so here in this room, you know, whatever it takes.  But you know, don't make a song. Yeah, I can talk.  you know. Just let me know you're there  and tell me who you are. Yeah.  stop.  Yeah, appreciate it. Just a couple of additional notes that I'll add maybe I remember when we were working on things. One thing that felt excluded by was you wanted to do a study of broad threat. That's something that wasn't figure out how to do that shadiyah jones: right. Right? shadiyah jones: No, I do agree with that. I do agree with that that's also another thing that could possibly be talked about by staff. How can you allow students to feel more inclusive when it comes to signing a problem, because that does make you feel very left out when that's something you want to experience. But think you have your disability that interferes with that, and I would love to speak to what's what's his name? Sitting next to you, Charlie? I wanted to speak to his point. shadiyah jones: What'd you say. shadiyah jones: Lance? Okay, yes, lance. Okay, I agree exactly. When I first came to Iup, why, it was very hard, because I came. I had took a class at Ib tech, and when I went to Iv tech, one thing I noticed is, it was so communal, it was so much community, and people would just talk to you, and they wouldn't care if you had a disability or not. They would talk shadiyah jones: when I came, Ipy. Well, now, when I came because I was already there. But when I came back to Ipy I just thought it was like, dang people! Aren't that friendly here? They just walk past you. Nobody stops to have a conversation. I noticed that. So I can definitely speak to that point of just like shadiyah jones: talk to me, hey? Ask me. You know what I need if you want to. Or if you wanna engage in a conversation, let's engage, because doesn't hinder me from doing that. So I can definitely speak to that point. I can understand what it says that for sure. shadiyah jones: And that's why I have. The 9 of scholars was really a big help, because it helps built that confidence, booster, to make more friends and to just have the friends you already have within that community.  Alright. So we're 14 min out from being finished here, and I want to give you all a chance to ask questions.  What question do you have for our panel, or for me, for that matter?  Who has a question.  Anything come to mind?  I think that last part really is.  I know from my colleagues, perspective.  rules. Yeah. And then I want to open that up a little bit sometimes say, Well, what? Sometimes? Wait?  should we? And especially when it comes to maybe not the content and maybe that prompts some questions, but that's something I feel pretty strongly about. We've been teaching universities. Education general's been kind of the same for a couple of 100 years.  It's probably time for some upgrades. And and I think this is one of those areas where we could, we could use some significant upgrades. But we keep doing the same thing. And maybe that's a topic for us all to talk about.  Great Charlie, and  going back to one team  and all kinds of ways to try Charlie. I'll turn again  ways of making that happen right, wishing.  pushing the programs that are the designing study abroad  opportunities to be in. So  people with mobility? Who watch your wheelchair users, inclusive of people who are blind, and people also who have visible are not apparent  disability, but we've been in compensation for quite some time  about that even back when Pant King was still here. However, we may quite  about the strides, how, and yet we still are very much able as universities where we're considering things from ability, wise instead of differences.  But there is compensation about that. And  and push towards how our university can change the technology in certain kind of ways to make sure that students can be involved, but also how, wherever this is maybe going to have a  something speaking to you, Matt, what you shared about building a home that is accessible with the ramp in it. Iii absolutely love that right. So thinking about well, do you have a board? Do you have something that you can put down for this going to be able to ramp up onto that train and ramp up so the will have to ask  the people that they're partnering with for the study of broad program. These, let's make it accessible on parking. But we're working on that.  And we have ways to go. But we are. Yeah. One of the buzz words that you hear at higher ed is high impact practices. Kind of one of the things that I want to say right after I hear that is, you know how and how inclusive are those in my background  they are. Let's figure out how we can, you know.  Does that generate any questions?  I see what bubbling up right here accommodation cannot fundamentally alter  the objective of the force. For example, if you need to do a certain thing to be able to say that she the objective of the force.  If you want to be a Ld. Surgeon.  and you have a disability, add will prevent that from happening. And that's fundamentally all planned a curriculum, if you say still vote for that right. However, in the midst of that type of a conversation. We have this thing called interactive processes.  So you just can't say  you cannot become the Ld because you are fundamentally altering the curriculum. You have to prove it. You have to have technical standards. You have to have things certification, certain things that is contingent upon reaching that we would be able to complete and satisfy a degree. Okay, fundamentally altering curriculum happens all the time. Meaning this  is that you modify right? You don't change you modify. So how can we get a student there? How can we make this happen? Test? This happened before, in United States or otherwise, anywhere else?  If that's the modification you do the work, the rigorous work between our office and other offices and other programs to get there. So we're not being exclusive. But we're being, we're finding other ways that people to be involved. And it takes processes that you literally cannot fundamentally say, let's change this.  Okay, when there's something that happens. Yeah, got it? Yeah.  Yeah. And we've lots of students navigating these with the help of Aes and others. When it comes to say, for example, low vision visually impaired students who's got to take statistics where it's gonna take economics, especially where there's lots of graphs and charts and kinds of things involved. You know, curves and such. You know, we've  we're always trying to find new and innovative ways to for students to be able to get what they need, the faculty. They want to find a way. But we don't have the creativity yet to figure out like I've been doing it for this way for 20 years.  I don't know. I don't know how to make this access.  hey?  A community of practice beyond just this university that's gonna impact so many other places where we really will become  university country, or whatever that  don't just play Kate, that we care  and and make sure that happens.  So you said some some interesting things there, and one the one that's sticking in my mind and pivot from this. But you mentioned like you're got a physical disability. You want to be a surgeon  there. There's aspects of education. Why, it may not be. You cannot have any wheelchair, and it be sterile in an operating room? That is a safety aspect.  People who are in wheelchairs who have not become surgeons and maybe do not know people in the medical field just simply do not know that  educating where limitations may exist is important. Telling them no is where the issue, because what you want to do is you don't want to just say no and kill the conversation you want to say, here is the situation.  Help me with your creative thinking on how you would overcome these items, because a lot of the times what happens is, anyone with any kind of disabilities will know cannot happen. That is not the right approach, because that shuts the conversation down. It needs to be. Well, that's an interesting idea.  Here are the limitations that we are up against right. Now let's work together as a team, and let's solve these problems. And let's make this happen. Let's do something that has never been done.  cause it's my heartbeat. I've been in this work for 1516 years  and my heart beats strong.  Yeah.  I've told many people this just recently. just because something is not possible doesn't mean you can't ask why.  And you're gonna piss a lot of people off that way. You told me. No, I can't ever say why. And you're gonna say, well, you can't let me say, why? Why? Why can I not be a search? Give me an answer that I cannot solve a problem for why? Because that's I don't care if it takes me 5 h of asking you the same question. If you cannot give me an answer that I'm like.  you stop me. Got it okay? Time to move on. I'll find something else. Now help me find something else that matches my desire. Maybe it's research. Maybe I don't have to be in as sterile of an environment. But you have to. In this goes to students. This goes to faculty. This is staff.  Be that that PIN that you're just jabbing it, twisting it, whistling your job as an advocate for yourself.  No one is going to update for you the 9 scale program tries really, really hard. But they're also updating many other people.  It is your job as an individual to advocate. I don't care how many people you miss all because I miss a lot of people, but you have to do that.  I think we have time a couple more questions when I see, Danielle. What's that question? Oh, so as a program that there's a lot of icebreakers. And thank you for that  highlight, just that you can think about like.  what are we doing? And how is this? Because sometimes you don't even know who's gonna roll? So you just assume that everybody can do it. So thank you for that feedback. But then, also, when you were talking about being a surgeon  like my mind went to  why, we have to like.  you know, Mds, just sit in a room and pull up somebody on a computer screen and pad usually, and touch here and touch here, which I'm like I don't know, but I feel like there are so many options where individuals could still  be in that medical field without being in that surgical, you know role where it has to, because now we got bench, they're literally robots and the surgeons in another room.  Why do I need to be sterile if I'm in a completely opposite room. You've got support staff that are in the or room. We've got our technicians in our our end who are changing out the tools on the robot. Why do me as a surgeon have to be sterile if I'm in the other room.  like I understand, if I'm not doing a da Vinci surgery. Yeah, I have to be sterile.  Is there a way? Is there a technology to sterilize all of my equipment? The answer might be enough. But you really have to ask those questions you have to challenge. You have to keep asking the why? Why? Why, some people scared AI. But I feel like there are some ways that AI can make that you know possible. Let's use them for good.  Alright! Well, we're we're coming pretty close to to time here. So I wanna I wanna thank everybody for showing up and being here and and being part of this conversation. And I love that the theme is a community of practice. Does that mean the conversation?  So so so thanks everybody. And I really wanna take an opportunity to thank our panelists.  and I and I might get some of the accolades for sure, Dia and Matt, and remind me if I if I'm forgetting something. But I do want to acknowledge that that Lance here has been named top 120.  Alright, humble fellow probably doesn't want all the intention. We will be reaching back out to to Youtube as well as we continue to move along with our community to get practice. shadiyah jones: Well, thank you, Charlie, thank you. Everyone. I appreciate it. See you later  regarding you know session today.  and they're still.

Zoom Recording of Nina Scholar's Panel Event

Moderator: Charlie Johnson, Director of Scholar Support Programs at IU Indianapolis, Director of Nina Mason Pulliam Legacy Scholars Program

Panelists: Shadiyah Jones, Matt Griffin, and Lance Varnell

IU Indianapolis Undergraduate Student Panel

Intent: The intent of Undergraduate Student Panel was to provide a space for IU Indianapolis students an opportunity to share their academic, social, and personal experiences as disabled students and students with disabilities.

Impact: This panel shared how their identify has shaped their experiences at IU Indianapolis, the challenges they have faced in higher education, how to be more inclusive in the classroom, as well as advice on how to best support disabled students and students with disabilities on campus, and what you can do to spread awareness about disability community.

AES staff member, Dr. Elena Silverman stands at the podium to introduce the moderator
Moderator, Dr. Corey Clark, clasps his hands mid sentence as audience looks on
Student panel and moderator surrounded by audience of staff and students
Student panelist, Chris Avila, talking
Student Panelist, Akaiya Bryant, talking
Student panelist, Selma Adie, talking
View of all four student panelists and moderator, mid discussion

Description of the video:

 Aye, next.  Thank you for joining us today.  The aesthetic awareness month is beginning of our efforts for creating a more outward facing and collective, successful educational service and community of practice  relationships and services into collaboration.  My name is lately I want to be yes, and my pleasure to introduce our moderator.  Dr. Corey, Clark.  higher education.  transition and university initially people, the doctorate adult education, leadership, advocate for diversity and equity and higher education committed to impacting lives education. He needs to make a difference, one graduation invitation at a time.  And now I will fashion  kind of  which moment which I learned  personally with disabilities person, which is something that I've learned.  Monday.  It's important for me to be here today. But also it's important to be an advocate for all students and as a person who's parents are there my identity is child of a deaf adult influence is my.  particularly as we move towards the community of practice. Simply  major Home town and something. There's a fun trap when we'll start. Folks are the closest to  Hi. I'm Selma. I'm a Biology major from Fisher. and I have to keep bugs.  Thank you.  Hi, my name is Christopher Popula. I'm a Biblical engineering student.  I'm originally from up North America, and it's fun factors. I like that.  Anything to do with numbers. I'm sorry, did you? You said you had what?  Hi! my name is Akaiya. I am a sophomore at Ipy. My major is is social work and a minor, and so I want to be a therapist, and a fun fact  about me is, I love giraffes.  Hi, I'm Sarah. I'm a biology, major.  I'm from Scienceville, and  this is other. It's a fun fact to be. He's actually my second. I can dog  couple of questions dialog. So  so my first question and feel free to answer it. And I'll just pose this first question. Every student can answer it as personally reflected on your journey as an undergraduate.  What advice would you offer to your high school sales regarding  navigating the college and academic life with a disability.  I can go first to say that I was not disabled as a high school student.  I do being disabled between my freshman and sophomore year of college. So if I, if I would get to myself, is video boarding myself that this was gonna happen  and encouraging my own results to seek friends, to have gone through some of their experiences  numbers.  I guess I'll go second for me. I entered college already blind and remain blind. So for my younger cell phone I could go back and tell him not tell him to get more involved with campus events, as it were, just to learn the campus better, just to be  more aware of the different resources available to campus  for me, I would tell my younger self that it's okay to not be okay. I struggle severely with mental health. I've been in another inpatient.  Not. Okay. Okay.  Sorry disorder. Just not to find me as a person  I would find myself it  good. When you think about  getting involved because I didn't figure a reason why we maybe wanted, you know, maybe didn't get as involved with it. Make sure  for that one. There was a like a  I don't know. For, like a example physics group just to get together, hey, we're gonna be some women common just because brows a lot of material, and they'll have to go forward to test to do the same. They don't really care, that's all problem. So they wouldn't have made that much difference  stuff like that. And then how much  campus activities are actually worth I was only aware of.  I guess, and then everything else is just there. Don't happen  any any other panelists want to speak to that?  I should go ahead and  say, if I struggle to find a place where  disabled people for centered apart from Aes, which isn't really a social  so I went ahead and start my own, which has been and that has just it's increased my involvement with single community, and it's increasing involvement of a lot of other people.  I  I'm really happy with that check.  And so  really quick, sir.  which are going to be in mind.  How was it? How has it been an undergraduate, disabled student? Of course student ability shaped your experience within the Indiana University, and that was community.  Hello!  I guess I could say something if I understand the question correctly.  are. I've had a more or less really good experience around the city, and then also on campus  fellow students, and then staff members and their professors overall. august  being  people are more willing to come up and start a dialogue versus, I guess in my head site they would otherwise  more long. I guess  they're more willing to come up started this session, just because, since I think it's a lot visible, they could see that some time I need help, or whatever it doesn't come up and just call either ask by any help or just introduce themselves, and then from there again I don't know. It would be different. But up there some of this experience is an opportunity. People just coming up with 30 conversations probably would have been otherwise.  Anybody else want to add to that, or speak, answer that question. I'll say it again.  How would you identify in mind? How is it? How, being an undergraduate with disabled students, with disabilities, shape, or experience within the ie. Indianapolis community.  I think for me because I like, I said, in and out of inpatient facilities. I would take a bit of absence in the fall. But what I found out was that like I feel like is really on your side, and I will work with you. That was a big concern about me being off for a semester and meeting in and out of hospitals  throughout my whole experience through iapy  that they are on my side.  and that they will. Will work with you  right else.  Sorry.  very willing, to come up and ask questions about him, and I've been able to make. I should feel people through that  I had an opposite experience where I was just very afraid  being in public with an invisible disability. And I isolated myself because of that  up until the point where I was like. Oh, I can make a social club. I can make a place for that place where I'm safe to be there. But in terms of just other students. Oh, your email looks so good. It's like  or just complement my hair. People have been very, very kind to me. I just thought my own head about things  this while we're here. Just as a moment. I want to  just elaborate more on that.  if you can.  Are you referring to me? Sorry I messed up  any barrier that I face, that it's more in Indiana law  is that when I came up to a professor and was like, I have just gone through something like, I don't have a diagnosis. I don't have paperwork. I have just suddenly developed an end of the disorder.  I don't know what to do about it. Can I get accommodation?  The answer was, I can't legally answer that question. You need to go through aes  Which was odd to me at the time. I didn't look into that, so I don't know if that was true or not. But that was an instance where I wasn't sure how to access aes or how to get documentation, because I didn't have  the time, energy, or resources to go to a doctor at that point in time.  And therefore could not get access to patients.  Hi, I'm so small sorry, Sarah. She does some work with Dr. Wars, and I I thought it was a wonderful opportunity for her, and she might want to talk about what she did with  check.  Sarah, did you want to talk a little bit about that?  So with Dr. Mars may  first semester like, if you I noticed a few issues and updated terms on the information on disability initiate added. So I've reached out her and the next search, able to do an internship and rewrite that  page 4, the K. 101. But that'll be opportunity. And to do a lot of research and work.  Thank you for sharing that with  while we're gonna do any other questions you want to feel, Ryan.  I did have one question for you. So we talked about it.  Yeah, it's called the visual advocacy organization at Wi. Our Instagram is PAO. Under. That is where we are.  Our information, like educational information, and also our events.  very next event is going to be March 20 sixth at 6 Pm.  Locations to be determined. But we will take. Excuse me.  we'll be doing a sticker designing competition and a mobility, a decading night. So if you have mobility for this different things like that, if you don't have one, or even if you do, you can participate in designing a sticker, the winner of the contest. Get it out.  So really, what our organization focuses on is one bridging with that between  students and their experiences and aes and other institutions at Ipw. Up to a certain point, we did not know where to.  Another thing is.  what's the question that's going to be awesome homelessness.  Okay?  So connect to that. If you want to start with  cool.  how do I explain the difference.  I have.  Thank you. In my coffee. I just  it's the most, and that's impacting it right now. And when I get through a  alright  people, when color was applied.  And lectures like yellow. We're having red text, followed by  just certain like color coding and certain. Thankfully, everyone that I've I've had  requested that, and no realize that they hadn't been considering that  but that's something that I just think everyone should be  be cautious of when my  for me  with for both of my classes, for every single my classes, since it's all that, there's a lot of diagrams that can't really be explained in a digital screen reader computer. So most of my  for my classes, which are basically when the professor is pointing at a graph.  they will show me where the professor is pointing out on the graph I have in front of me, instead of me, needing to ask the Professor to stop every single time to clarify, since professors most of the time say over this over here, or  they point somewhere to the other side of boards like at that point you have this reaction, sorry, and so forth. And so they would just show me on my lecture notes, or they would draw the graph on paper to show me where exactly the professor  project.  Alright, so we should kind of miss it a little bit, and I maybe we can get something, make a little bit about talk about some accommodation, but discussing accommodation  when you say department  most of the time  when issues come up, they're either on it that day, or they spotted, which they spotted a week or 2 with it.  So we have a solution ready to go when it does come again. But again. Still, the first person to go through this degree path is, there's still issues that pop up that we haven't talked  but most of the time what they do, for everyone is motivated to  where I had just received disability accommodations  30 min before finding  we're able to work with me on picking up  assignments that I missed the last that I missed and  helpful because they'll be there with a  gonna get up.  sure. anybody else  right? I'll take a quick moment. Do you have any questions from the audience? Do you have any other questions?  Oh, so go ahead and so I we wonder if there are any  Oh, I'm really  solve problems in my regular life. So I'm really good at that, and coming up with solutions. So now it's  again. When it comes to the  Academia itself, let's say, be involved in any way with the possibility. Maybe in some degrees. Do not have my children.  I'll take it.  But I would say in general,  people just being curious how I can craft.  allow me to interact with interesting people, some good, some bad, but  that's possible.  Question here.  I 2 ads  beautiful city.  let me see.  and  tithing all throughout the schools. I make  choirs. I posted it all around the campus.  I reached out to old organizations like the Lgbtq enter and after the event ended it was actually really good turnout  that came. But even with that small amount of people like, I feel like you may like a big impact in a spread awareness, because I feel like. Not a lot of people know that having a stutter.  if disability, because it affects me every day throughout my life, especially like communicating with each other, and everyone that I need across with it does affect me, but I get positive one that  for now.  But I was a freshman, and you know what I was doing, but I knew, like it was really important to like  spread awareness on it.  I have to answer that question.  I was just going to agree with you with.  that'd be more resourceful and adaptable. But, secondly, be being able to problem-solve thing.  slide that.  And just now, out of  those, the importance of everything increasing awareness, right and spread into word. And so when you think about including in the classroom for students and students disabilities having students in the classroom, you find the  the benefits.  Does this benefit everybody? When we think about the diversity of like our education? Right having diversity is what makes it our education. It shouldn't right, we think about having students with disabilities in the classroom then, and  the inclusion and and and having students, and get included in the class meeting that benefits every student. When you think about that, we think about inclusion in the classroom.  can you repeat that again. So this is so we think about include, do you think inclusion in the classroom for students with and without disabilities, benefits? Every? Yeah. It's important. It's like everybody, should be  included. I'm all about being inclusive, and in any way I can. For example, the bathrooms. I make sure.  A little chair of flexible ones, because I know that there are people that actually  needed. And I try to be to everyone that I come across.  and being on campus now in the classroom.  I haven't really had a good experience, just because I feel like people think like I'm I mean making a joke like sometimes, and and  did I? That's better. And I feel like that's  I feel like they like make it as a joke, because people do have a setter. And actually, 1% of our population has a setter and so it's a really  commenting and so  be a  inclusive to me and be respectful.  I just wanna answer that question. Do you think inclusion in the classroom for students and without disabilities benefit?  Absolutely and  a big reason for that. Is that a lot of people don't know they're disabled.  A lot of people like if you have  things back.  don't show up the way that people think they show up. You could go 20 years or more without knowing  that you have something that's setting you back. So when a classroom includes everyone, even if they don't know there are. There are hourly disabled people in the classroom that is making the path easier for those who have hidden disabilities, or don't know that they have.  I've also feel like, while was on campus like, especially on the and the the campus center. Like, while I was ordering food. We had people like and just kind of being like removed. So I haven't really like had a lot of good experiences. Wow, like  food on campus. That's something that I feel like should be spread more awareness on  other than that. That's something I can can really think of. A lot of my classes. I do take office online just because I have a lot going on all throughout the week with these appointments. That I have going on because of last year. It's really hard for me and my mom is actually paying  my funeral because she knew I was not gonna be here for long.  Yeah.  And it is I've been. I struggle a lot with mine as well. but really bad. So  I've been definitely in a lot of  probably been hospitalized, maybe not 5 times within the past 2 years.  So  appreciate you sharing with us.  And so  yes, if anybody else wanna answer that question and  and yes.  I would say to a point, it does definitely it does to a point just to know.  not understanding, or what  on the board visually. That's why, or everyone else that would take.  This is important.  Bye, bye. that were activated.  you can read it.  I never! I wouldn't even understand some of the words. And so, in being able to, I had to advocate for myself.  and I would never forget an undergrad going into a professor like, hey? I don't understand that English is my second language. Can you tell me? And literally every day after that met with me after 5 every Thursday, and so being able to, you know, to say, Hey, just growing up, it was  that was different, and I never wanted to be associated with it right? And so it took me going to college to really find myself, and I'm my identity and say, Hey, you know I am a child, and I have my experience in that, and that this simple interaction  educated her way to be able to to be. Maybe I don't have. You know it's my identity, right? And that's something. In terms of experience of the child education and being able to learn from student stories. This is, that's the essence of what this hired  do should be with hope. So right? So that's why today is here. Because I learned something every day just simply in power. I write my emails, just learn something different today. And so hopefully, we can all take away from something up from today. But I'll pause for a second question. Do you have any questions?  Think about inclusion and sharing a lot of times. It's up to the disabled students advice on how to make you take it off to the students. You guys are going to.  Oh, yeah, I think it's  no answer first. And I would disagree with just  over the years when other people have decided that I needed help. It was based off of what they thought. I needed help with versus what I actually need help. So I completely, Professor, to be like, Hey, I need this, or I need that, or I can. Actually, I have this disability, or I need these accommodations. I don't think it should be on the professor or anyone else other than to basically click, just because too often I've seen  that when you plan someone else's  understanding of how to best help most of the time. It doesn't do anything, and other times actually move detriment.  I also agree because with having a center like people will like  pause for me or finish lies.  and I tell them, like I am capable of speaking. I just need extra time like. I don't need you to speak for me. I'm able to speak for myself, but I just need you to be patient with me, and that's something that I constantly have to advocate every person I come across with, because I feel like it is a natural response, like, when you see somebody talking, you just wanna you finish your.  But like as a person who setters, I'm also involved in a a national organization for people who setters called friends. I've been a part of that for organization for years. I spoke on panels. I mentioned people all around the world. And so I can speak for the whole people who started that we are capable of speaking. We just need extra time.  I think it's an issue where  there needs to be more education on what isn't isn't okay.  because I I've also had like experiences where I've had to  like carefully explain like, no.  I can't use the stairs.  That seems like it would be obvious. That like you shouldn't expect that.  But I  disabled students through.  and how it should be. That sometimes it just doesn't help. Sometimes it  is more of a detriment. But  clearly, I do think the problem is just not having to install it to diverse groups and not being educated on what you think is located?  I just wanna answer that question.  So I also have multiple visible disabilities on my disabilities very day to day or some days. I can't even get out of bed. Other days I'm using one team some days I'm using 2 canc. And my question, how did you all learn about aes? Because I was an undergrad student here, and I never knew, maybe yet for the thing when I was a student here, so I wish I already know, when I was a student, that those services were available  cause. I also struggled up with stairs. I struggled with learning disabilities. So how did y'all first find out about aes  when I first started? I think it was my first degree  the I learned today. Yes, because my advisor at the time.  I think it was through something called the Bridge program.  and the first week I was sitting next to name Sarah, and she looks, helping me with a whole bunch of things.  and then the  advisor for us, Professor, I don't quite remember what they were.  pulled us aside Monday, and said, Hey, we should go to this office there. Here's the number. We set up an appointments go, and so aes office. We had a meeting, and well, that was that  it took me a while personally. I prefer if I went through my advisor with an issue that would send you back in class.  and I'm not gonna say names. But I was given a list  that does not help me in my classes. So it didn't take me until the middle of my end of my sophomore year, until someone told me. Oh, you can get accommodations where to get how to get them. And that's a big reason why it started the organization that I did, because I don't want people to have to wait as long as I did.  We get accommodation.  I think.  Research. I found a zoom. The  reading I did, for it's the the documentary is called my beautiful post.  Other and I kind of did my own quick research. And at the time the the director was  Dr. And  Mr. Crackin first name was Kevin. I reached out to Kevin, and then after that it went. It was like history. But I found out there. Yes, by doing my own research, but I really like how my  professors they definitely advertise aes and I feel like, if I did not.  If I did not do my own research, I would have found it through my professors, because all that I pretty much every time. A new class to start, I get all the the resources available for Iup Y is always a yes, it's always there  research. Actually. when I was a senior in high school and applying to colleges, that was one of  I decided factors with talking to disability services at each college before  second.  So  so on the opposite side of that, what do you think may prevent about students from being able to to utilize services, or maybe  I see and change the last of students knowing about it as as much as aes tries to push the fact that they accomplish. They are here  it. Freshman coming in just don't know and they don't know sometimes that what they have qualifies as a disability what they have qualified for accommodation, and there are things to help them through their classes.  I would say  opposed. I'm not sure about them.  I have to start dealing with the  equivalents from Purdue. People  think about the impact of that split  students and  not maybe, answers on us.  I feel like, kind of what?  Second.  okay, kind of what? Almost said that they are a lot of invisible disabilities. And I feel like there's a lot of  shit  there, real times about what is a disability and what is not a a disability like. Obviously, someone that's in a wheelchair, someone that is blind. But there's also like it's kind of like an an umbrella of the fact that there are. There are other things that qualify as a a a disability which kind of what I think that kind of hesitant people like to reach out  to get power  panelists. Wanna add to that.  And so the disabled community within the university.  couple of things here and there, so things that you all want one more time in your current role as an undergraduate. How can you contribute to belonging for the disability community within university?  I feel like just spread awareness, because that's what people know. Kind of like what  Thomas said about like it's not working, you know, definitely takes a lot of advocating, because as somebody that that is not didn't  disabled like if they see the elevator not working that. Then they'll just go a different way, or they just take the stairs. You know that type of thing. So I would say, I definitely take a lot of a a a vacation.  anybody else.  So  so hear me. So I wanna make sure  questions.  What do you wish your classmates. Just folks on campus  knew about what it's like to be a college student.  I think. Kind of like asking us like, how can they support you, because I feel like some people like like, Oh, like I feel like  next week for anybody, because I don't know whether speak for what speak for myself, but like kind of like what II mentioned earlier about people.  finishing my so  sentences for me. I feel like, maybe them kind of like asking, How can they support me saying like, Oh, do you prefer just for me, or when we are at a restaurant? Did you want me to order for you kind of like them asking me like, How how can I support you?  Yeah, what would you want? Either your classmates or anyone on campus to know what about what it's like to be called student navigating with the disability.  I would certainly want professors to know that.  It's not easy, and it's really difficult when you're experiencing in your life to prioritize like an exam or a class.  I feel like a lot of professors. feel like it's it's do or die in terms of their assignments. When  for us it's way less serious because we're just dealing with a lot more.  I don't answer very much  renewed.  Okay.  I would say.  I guess in general just that they don't have to constantly keep apologizing when they use the word look for what  other than that? It's it's from my experience it's everyone's been  pretty good and pretty mean, the same as everyone else.  I haven't really been able to tell the difference one way or the other, but except for the  when, some, when they're saying, Look your watch or see this, they would always they would always be the awkward pause, and they would start apologizing. It's funny the first few times  everybody else want to have. You know, the Panelists want to add to that  what you said, people asking how support that I would talk to like that. But  and  instability, even if the labels is different, and even if the labels the same and understanding difference from person to person and not assuming because I've seen this before, it's  the same as it was, and treating each individual  based on that  purchase.  Alright. And so  and so that was the wow. That was the question that I'd like to add.  You, you know, like, what can you help us to understand about apologizing?  We're using word such as look. Rc, so what I mean by that is that it's  for myself and any other black person I've met throughout my life. I've never met someone who was overly offended, or even couldn't notice of when someone said, Look at this or watch this video. And what I mean by it's undoing is that it? First, I feel that  as they're trying to understand.  and the professor or the student, or whoever.  Well, if you watch this video, they do a good job of explaining. But like. Oh, I'm so sorry  apologizing, and it just takes time. That's unnecessary. I didn't really notice it. And even when I'm talking about videos, I'll be like, Oh, I watch this video or I'll look over here for this or whatever. And so what I mean by word choices just being annoyed.  It's just  it's just those simple things. If it's something they use day to day with anyone else. It's special exception when using it. And then  you're the one who's calling it out. If someone else calls you out. Okay, I guess I personally don't see why they would, but maybe someone would for it. But unless they  person taking issue or the side person, I don't see a reason why you need to.  especially if I told you the first time it was fine, didn't really react to it. I don't think we need to apologize 10 times  relatively usage. Believe that I know what  I say. It's fine.  final question will be wrap up.  How do you mention a little bit about  I think to be patient with me and with us.  because I feel like we are. We are trying our best.  And then  justice and awareness movement.  Yeah, like, I said earlier, like just asking me, or as like, what's the best way for us to support you. I feel like that's the main thing that's like people make us assumptions. And then then, like  everything goes wrong.  I would also add to that and say that a lot of allies feel like they're doing something  or decide  so that's not like being educated and letting the person be independent of us.  They are asking for help.  and just so just to say that we all ou our normal people kind of like what Chris said. You know, like we we are, we all are normal people.  I would say, for the Allies supporting  I would say they don't really have to do anything just  just like whoever is.  Whatever event.  campus activities such as like the  there's probably a road seating or school riding or school wrestling huge frame  to certain themes such as they'd want to play, that  I've found that most people who have disability, the more visible, the more visible it seems.  the worse it is, but seems like a lot of people just do.  unless they invited  folks and faces  anybody else.  Alright. So as we approach time. I want to first take an opportunity to say, but it's please give us  provided for sharing stories. Hopefully.  folks in the space of learning something the way I have today. And so before we wrap up today, I wanna make sure that we take time. Our surveys available. And I think those surveys, I think on the around the tables. And so please, we wanna get to to user feedback on today's event. But again, I wanna make sure. Thank you all for being here today. Yeah.  yeah. feel free to. Yeah, I did the work.

Zoom Recording of Undergraduate Student Panel

Moderator: Dr. Cory Clark, Director of Diversity Enrichment and Achievement 

Student Panelists: Akaiya Bryant, Selma Adie, Sarah Zetzl, and Chris Avila

The Gregory S. Fehribach Center Student Panel

Intent: The intent of the Gregory S. Fehribach Center Student Panel was to highlight the work that the Fehribach center does to provide extra-curricular experiences for students with physical disabilities by providing access to field specific internships for students at IU Indianapolis, and many other schools.

Impact: This panel highlighted the many ways in which the Fehribach Center’s internship program provides access and support to students with physical disabilities as they begin to consider what post-graduate employment might look like. The panel conversation provided insight into the depth and breadth of the program and the positive effect it had on the student’s experience both in college and transitioning to the workforce.

View of the panelist taking the microphone to answer a question from the host with ASL interpreter on the right

Description of the video:

 Promoter skills for me as well, but those aren't nearly as prominent. So throughout  my schooling, when I was a lot younger I had leg braces for a good period of time.  Just to help stabilize my walking, and the way that I moved throughout the world. And then.  as I got older. I didn't need those anymore. Going through college, you know. That wasn't something I really had to focus on as much  because over time they had learned. You know, what worked best for me.  And so  throughout college, I didn't actually need really any accommodations.  I basically created my schedules to the best of my ability, of course.  to make them  more cp-friendly for myself, so to speak.  and  so I didn't necessarily take super early classes. If I knew I had to drive to campus.  That wasn't always avoidable definitely, you know, had its moments, but that was fine.  And  there were times where I would space out when I had classes throughout the week. So when I lived on campus my first year of school.  for example.  I would have 2 or 3 classes on Tuesdays and Thursdays, let's say.  and  I would space them out enough to the point where, if they were in 2 separate buildings. I would have enough time after one class  to go, and either  go back to my dorm building for a little bit to prepare for my next class, or.  you know, go to the campus center, do something there, work on homework. What have you?  And then still have plenty of time to walk to wherever my other building was, if I needed to. Thankfully, as I got through  undergrad a bit further and got into more major specific courses.  I primarily stayed in the It Building, so I was able to get a disabled parking pass  to park right next to the building.  for whenever I had classes, and then I could just show up, go to class, do what I needed to do, and go home.  And that ended up working really well for me. especially because a lot of those courses ended up being  a mixture of hybrid. So half of the time I would be in person  one or 2 days out of the week  to go to a 2 or 3 h lecture, and then the rest of my classes would be asynchronous online.  So that's kind of where  that differs for me, I think, compared to  other disabled students or students with disabilities, is  I haven't been a student so far. That's needed a lot of accommodations that others might  want to have. And the same is really true for my professional life.  I work from home. and so there's not really anything that I need in that regard.  But if it were to come up, I know that I could ask for those things and my supervisors, and I would find a way to make them happen as necessary.  2 things stand out to me, Cameron, from from what you've said  one. I'm sure the Aes Office can tell you how many students have disclose their disability or register to disability with the office.  but they can't tell you how many students with disabilities there are on campus. because not every student with a disability chooses to or needs to disclose the the disability. And it sounds like that was the case in your situation.  The other thing  that I think is kind of a cool thing for this campus. I know that that you all that work here will say, Well, no, it's not perfect. It's not, you know. There are physical accessibility issues, etc.  But this concept of universal design creating  built environment with accessibility in mind. So you don't need to have to go back later and retro fit things to to create accommodations for people with disabilities. Sounds like there's some good universal design going on on this campus to where you, as somebody with a physical disability with Cp. Was able to navigate campus successfully  without having.  apart from disability, parking without having to request any specific accommodations.  I might ask.  what was your situation like  in K. 12, and let me maybe preface my question with a little bit  from over the years, working with college students, with disabilities, I would hear horror stories  from students with disabilities, both physical and and non-physical  about what happened to them in K. 12. That  well-meaning people in K. 12 didn't know how to accommodate them. Didn't have the resources in place often segregated  students with disabilities. Who would  be college material would be planning on going to college with with students who would not be going to college. What was your K. 12 experience like as as a young person with a disability?  I think that's a really good question. And I'm so glad that you've asked that. I think that's a great  thing to kind of understand alongside all of my undergraduate experiences.  admittedly, I don't remember a lot of my K 12 experiences as far as earlier years in school. I don't remember exactly how those played out  in terms of my disability, but I know. I believe, throughout elementary school. and  at least part of high school, so really elementary through early high school. I had an Iep  at 1 point. And then, when I was in high school.  I had what was called a 504 plan.  and that because I remember that more. The 504 plan allowed me to  actually have 2 separate lockers in my building at the time, because the building that I was in  in my school district.  I am. So I'll preface this a little bit I'll backtrack  I am also a graduate of Hamilton, Southeastern  and when I was a freshman and freshman in high school. They were still building onto the main high school building.  So I was actually in a previous junior high building. My first year of high school.  and that's where I had 2 different lockers, because one of my classes throughout the day was  on the second floor of the building. And I think if I'm remembering right, I'm pretty sure that was  A biology class, or some sort of a science class that I had. That was on the second floor. and I think before that I was all the way on the other side of the building  for a completely different class. and I knew if I were to go to my  regular walker, so to speak.  to get  things out before different classes, or put things away before different classes, that I wasn't going to make it  in time, because I think there were maybe 5 or 7 min passing periods.  So for me to go from one end of the building to the complete opposite end of the building and upstairs, and get things out of my locker to get to class on time.  That was a bit of a struggle.  But thankfully, you know, all of my teachers were super accommodating with that, and I never had an issue. If I was  slightly late getting to that one class.  because they all knew my situation, and it wasn't a big deal.  so  that would be my most recent  memory in terms of having a physical accommodation for something like that.  Even before that, though I would say throughout my  gym classes in school, I would say that I had accommodations because my gym teachers knew my situation. and they were like, Okay.  you know. Please still do everything else or everything that everyone else rather is doing.  but they didn't make me do it the exact same way. So  I don't know how familiar all of you are with the pacer test.  Do you? Do you know about the piece or dust? Okay, so  if you don't know about the pacer test, that is basically a running exercise where you go from one end of the gym.  or wherever you have your gym class to the complete opposite end of the gym  before  a tone goes off like you have to get there before a certain tone  goes over the loudspeaker, and that's fine.  except I don't run at least not very well. Running is not my forte. And so  that was one area where I knew this was going to be a struggle for me. And so my gem teachers were like, Okay.  you go to the middle of the gem while everyone else goes to the complete opposite side.  And then you go back. And I was like, say less. That's a great plan. And it worked really, really well.  so that is one example of a different sort of accommodation. That wasn't  a real accommodation, if you will like. It wasn't something, I think was documented at the time. I think they just knew.  That's one example of another accommodation I had had  throughout my school years.  And it did. It worked really well as long as I gave my best efforts. That's all that anybody else was concerned with.  I think fully never had any issues with other students in that regard. They all kind of knew my situation. and they were all super, you know, affirming and helpful where need be. So I got very lucky in that department.  I would say. Those are probably 2 of the more prominent examples that I could give for that  solely because I just don't remember enough about the earlier years of school to really give background from that perspective.  Okay, one more question along those lines.  One more unscripted question, sorry, Cameron.  one of the research  studies that I was fortunate to be involved with years ago was a study. It focused specifically on college students who are wheelchair users, but the the broader principle applies on what factors  led them to realize that they were going to go to college. What was involved in their transition to college. And then parents were also included in this study.  and one of the things that that from that study that really still stands out to me.  was parents saying, despite the presence of the disability, it's like no people in our family go to college. All of this students, siblings, went to college. The expectation from day one  was that he was going to go to college.  We're  to the best of your recollection.  Was  that always the expectation for you, Cameron, that that you were going to be? I mean, even though you were receiving an Iep and a 504, that those were always focused on preparing you  for the college track to to go on and get your college degree at some point. It's a long, poorly worded question. I hope you understand where I was getting it.  I think that's a great question, and I'm you know I'm glad that you followed up with that.  I do feel like that, was the expectation that I kind of had with  family, especially with my parents.  Growing up. There wasn't.  I say there wasn't a focus on my disability by my parents, but  I feel like that's not quite the right wording, though I also feel like.  unless you've experienced disability yourself, or have worked closely with disabled people. it may not make as much sense to you.  so I'll try to elaborate. With that I feel like my parents, and really  all of my family.  you know, saw my disability, accepted my disability for what it was, and did  what they needed to do to help me, you know.  be the best version of myself that I could.  But they also didn't  PIN that to me. so they didn't  want to raise me with limits  in my head, so to speak. So in that regard I would say that I wasn't really raised any differently than an able-bodied child. I mean, there were things that definitely  were different about my upbringing than  a typical, able-bodied child's would be  You know I went through all kinds of different physical therapies as a kid I went through Botox treatments as a kid to help my leg muscles.  I wore lake braces up until I was about 12 or 13 years old.  so there were lots of things that they definitely did to help. you know.  aid me in living with a disability, but they definitely didn't put limits on me, and I think  college was a sort of expectation.  Though I think if I hadn't of gone to college, I think they still would have been supportive of that as long as I knew that it was what was right for me.  so I'm really. I'm really glad that you asked that. That was a good question.  Thank you, Cameron. And then. thinking again about your experiences here. and as you look back. what what would you share with faculty and staff  at Iu? Aye. about your experience?  and about more broadly engaging with students, with disabilities, and then the more broad disability community.  So  out of my own experience, I never had any issues personally on campus again, because I didn't really need specific  written accommodations that were through the Aes office.  but I do think that it's really important for faculty and staff to keep in mind that not every  disabled person or person with a disability  as a visible one. not every disabled person that you look at is going to be noticeably  disabled.  and to that effect as well. Not every student is going to need the same accommodations, even if they've got the same disability as another student that you either have.  you know, currently working with you, or one that you've had previously.  It doesn't all work the same for every single person. And I think that that's something that a lot of people are aware of. I think when you say that to people they're like, yeah, that makes sense.  But I feel like it's also something that is really easily forgotten about. At the same time, I think it's really easy for people to  look at disabled people and disabled students.  and just expect that they'll need the same things that everyone else has needed. And that's not always the case. So I think that being willing to foster environments where your students or colleagues  are comfortable enough to disclose their disabilities if they want to and being willing to  really listen to them and hear them out about what they need versus what you think they might need is so critical. because ultimately disabled. People know themselves best.  You can be, as you know.  good, spirited, and is helpful of a person  as you would be in any other situation.  but as able-bodied folks. You won't know a disabled person  like they know themselves. And I think another thing that ties into that a little bit is the fact that accommodation needs can change. Even if you have a student  or a colleague  working alongside you. That's previously had one set of accommodations that comes back  the following year, and is like, Hey, I actually need  these other 3 things on top of my previous accommodations. And you're like, Whoa!  Those weren't there before.  Maybe things have changed. Maybe they've realized in the span of time, you know, between academic years that they need something different.  and sometimes it really takes trial and error with that sort of a thing. Sometimes you don't know whether or not you need an accommodation  until you've sat with and experienced it, you know. You might think.  Oh, maybe I want to have an accommodation where I can get more time added on to my  testing windows to take an exam.  Maybe you think that's something you need. But then you go and you start taking exams throughout the year. And you're fine. And you're like, Oh, actually, I don't need that as much as I thought I did. Things can change.  So I think, being able to be open and be fluid with  your colleagues and students, and just being willing to hear about what they need without  assuming first is so critical. And I think the more that people are willing to be  open about that with their students, whether they've personally experienced disability or not. Will ultimately  helped foster areas where everybody's comfortable to bring things up as need be  because much like you, said Larry. There hasn't been a time in my personal college experience where I felt like I had to disclose  having CPU, but  that also made it a really nice thing, because if there was a point where I wanted to disclose my having Cp. Even if it was just for the purposes of bringing up something relatable  in a class. I knew that I could. So I think, being able to have an open mind about those things, and just be willing to hear how what a student or a colleague has to say to you about their disability  is so critical to making them feel welcomed and heard and really seek.  I think that's something that does a lot for people.  and  I know as well that asking for those things can be really challenging. It might take a student or a colleague a lot to go to you and be like, Hey, I would like to have this accommodation.  Even if they are relatively open about their disability, it can be a challenge to  except the help for that.  Sometimes.  because I know a lot of disabled folks, myself included.  sort of have. or can have.  a sense of hyper independence  where  you know, if you're raised by people and around people that  acknowledge your disability. But don't  you know, keep it as a pinned label, a defining factor of who you are?  then it can be really easy to just think, oh, I can do this.  but with everything.  And that's not necessarily untrue. But it's also not entirely true, either, because sometimes you do need help doing different things.  and much like I said a couple of moments ago.  your ability to do things can change as you age with a disability, and I think  being open to being receptive of that as well, and trying to keep an open mind with professors, colleagues, you name it  with that in mind is also helpful. I think there has to be openness on both sides.  Or at least a willingness to be open on both sides to really make  that sort of a situation work  is that is that sort of the answer that you were looking for. Do you think  that's a much more thoughtful answer than anything I could have envisioned. Thank you, Cameron, that that really was  fantastic, and as you were describing that and the  level of trust  that it takes for a student to have that kind of conversation with a faculty or staff member.  I just think, and how discouraging it is when you've mustered up that courage to have the conversation to go and then be shut down.  which we know unfortunately happens, and and that may.  Students may not be receiving accommodations they need, because they they reached out at 1 point and and brushed aside by someone and fortunately, that wasn't the case for you. Ii really appreciate that answer, and a quick follow up.  you're describing very much  your disability, and I've heard you use language person with a disability disabled person. And and and we hear person first language, some we hear identity. First language, some  sorry to kind of put you on the spot here. This is off script as well. But as you've used those terms interchangeably, I guess I would just be curious as to your thoughts on language  with disability, your perspective as a person with a disability disabled person as well.  So I think that's a wonderful offshoot.  and I was going to touch on that, anyway. So I'm glad that you asked.  the difference in choosing  person first versus  I'll say diagnosis first language, because not everybody holds their disability as an identity. Some do. For some people.  A disability is very much a big part of who they are.  And that's wonderful. I'm very much that same way.  Because Cp is not leaving. It is here to say  so you know, from that perspective I choose to embrace it. And I think  you know again, that's something that just varies from person to person. And  ultimately it's best to just ask  if somebody is  willing to disclose a disability to you.  it's better to ask, do you prefer person first, or diagnosis? First, identity, first, language  versus making the assumption that they prefer one or the other based on how they might talk about their disability. And  and that's why I've sort of used both interchangeably is because I know people listening probably have heard or seen both in regards to disabled people.  And it can really go either way. But it's just personal preference.  For myself.  I feel like I've  experienced a lot of time, especially  in  childhood. K. 12, sort of.  you know, time frame where  my identity as a disabled person wasn't focused on  in my general day-to-day life so much that I sort of framed being disabled as a bad thing.  and that's not quite the right wording I feel like, but I know that there's a lot of  negativity  surrounding the word disabled like people here. You're disabled, and they're like, Oh, my gosh!  Like, what do you mean? You know, people are like, Wow! That's such a strong word. And it's like.  no, not really, at least not for me. It's not. And I think  that's something where  I wasn't super pressed either way about the language used for me growing up. But then.  you know, going into college, and really sort of figuring  more of myself as a person out.  that made me realize that it was okay to call my myself disabled  whereas previously I hadn't really felt that way, because of all of the stigma and sort of negativities that come  with that ultimately. Still, today, I don't really mind.  You know what somebody uses for me in passing, but I don't want people  to be afraid of calling me disabled and of acknowledging my Cpa because ultimately, even though it is mild and doesn't currently affect  as many of my day-to-day things as somebody else's Cp. Or other disability might  like. I'm stuck with it. It's gonna be with me forever. I might as well. you know, lean into that where I wasn't doing so, or wasn't maybe  quote unquote, able to do so  as a younger person.  ultimately, though, for everybody else, just ask  if somebody is open enough and willing enough to tell you about their disability experiences.  The best thing you can do is just to be open and just see what they want.  It's not about what you want, and that's I know that sounds harsh.  But it's really not something that you can take personally. It's ultimately down to what the person with a disability.  once for themselves.  and that should just be what you proceed with.  I mean, if you're you would want to make somebody comfortable.  you know whether they're disabled or not.  and that's one way that you can do that is by asking what they prefer.  And going from there.  Well, said my friend, well, said  little bit about the ferry box center. So I'm I'm the director of this thing called the Gregory S. Ferry Box Center. We're headquartered just down the street from here at Eskanasi. Health  named for a guy named Greg Ferrybach. Obviously, Greg is a pretty prominent attorney person with a disability here in Indianapolis.  Very well connected fellow. He's currently the chair of the United States Access Board, which is a Presidential appointment. The top governing body for Ada regulations. Years ago Greg's Ball State alarm was on ball States Board of Trustees, which is a appointment by the Governor, is also on the board for that oversees Eskinazi mayoral appointment, so they've been appointed by lots of public figures.  maybe 15 years ago, in my time at ball state as director of the Disability program there.  Greg asked me a pretty profound question. said, How come? I never see other people with disabilities in leadership positions, boards, etc.  Then the follow-up question, what are we gonna do about it.  Okay, we did. A lot of ball state has a lot of students with physical disabilities which we somewhat broadly define as mobility related orthopedic, visual and hearing  ball state, long history, lots of students with physical disabilities, lots of alums. We talked to several alums after Greg's questions and current students.  and found out. Unfortunately, too many of our alums with physical disabilities  were not equitably employed after graduation.  and so in talking to them, we're trying to find out why there's a lot of reasons why  one of the reasons was too often our ball state students weren't doing internships.  Internships are great. You're critical for everybody.  Let's the student gain that real world work, experience. Give him her them the confidence that they can do the work after graduate. All that good stuff that comes from an internship  internship is also for the person with a disability. It shows that perspective employer  that the student can do the job. They've done the job in an internship that that employer might be thinking stereotypes biases about the person with a disability, but they see that work experience through an internship that may offset some of those things.  So we start this little internship program using fairybox connections with one ball state student 1012 years ago  at Escon health full time paid internship  it. It took. Escanazi asked us to send a few students the next year, a few more the next year, etc., etc., grew to the point where Eskanazi asked me and my colleague, Carlos Taylor, if we had leave ball State. Come.  you know, expand this thing. Start recruiting students from other colleges and universities, and bring on other employers to host students. So we now recruit students with physical disabilities from across the Midwest.  bring them here to Indianapolis for internships and positions related to their academic majors their career goals  for people that come from outside the Indianapolis area. We house them. I'm pointing behind me down the street at at the river walk apartments. Here. We do a bunch of professional development for interns, lots of networking, etc. The goal behind everything that we do at the ferry box center is to make sure, really talented students with physical disabilities  get the experiences they need, so that they become great candidates for equitable employment after graduation. We've had now  200 students intern through our program. Those 200 students have done over 400 internships students can intern with us multiple times. We've had 40, some different colleges in the program. Send us students. We've had over 40 employers, host interns from the program. So  most on site, some hybrid, some remote. We'll do whatever we can to get the student a good paid work experience through an internship. So that's a not a little bit. That's more than a little bit about who we are and what we do.  But that sets up my next question to you, Cameron.  So would you mind talking to us a little bit about one, how you got connected with us. and and 2 the types of internship, the the internships that you did through the ferrybox center.  Absolutely. So. I found the farebox center in my  junior year of undergrad. And it was basically like a stroke of luck, almost  I had been looking around for all kinds of internship opportunities.  throughout my sophomore year, going into my junior year.  and I edible hide to one or 2 here and there. But I got rejected, and I was like, I really wonder if there's something specific for  disabled people to enter through, because I know that there's scholarships. I know that there's different.  you know, avenues for all kinds of college related  experiences.  That are specifically tailored for  disabled folks. And so I was roaming around the Internet and just happen to assemble up on the Fairbox center. And I was like, Oh, that looks really interesting. And then I saw that it was specifically for  students with disabilities. And I was like. Sign me up  and so I  you know, I went ahead. I looked at all of their criteria and things that they needed.  and I decided to give it a shot, and I sent in an application.  and then, I think. not long after that I think I met with Ewan Carlos. To sort of do a vetting interview to see if the program would be a good fit for me.  And sure enough, you both took me on  and then I,  you know, proceeded to start with you all that June. So that would have been June of 2021.  I want to say that we did our initial interview. Get to know. You see, if I was a good fit  conversation, I think that was probably in the February  and then I want to say it was probably end of the month early March that you guys were like, yeah, we'll take you on  And so that's that's how I got started with the center  and since then.  after that initial internship in summer of 21,  I then had a follow-up internship in my current department at work.  That fall. That was.  I believe it was September through just after Thanksgiving.  and then I took about a month break, and then I interned with them again.  In the following January until Maine. Or no. that would have been January until  August. Actually, it was So I guess it's 3 internships in total that I've done just one really extended internship.  and  so that's that's all of my experience with the Fairbox center. I think it's a wonderful program. I think you and Carlos do  incredible work. I know all of the interns do incredible work because I see them.  And I'm still connected with a lot of my fellow interns from my first internship. I'm still really good friends with a lot of people. and it's just. It's been a great great opportunity. I'm glad that something like that  exists, and I'm glad that  you know you and Carlos and Greg, and everyone else that you work alongside has chosen and dedicated yourselves to  taking chances on disabled people.  because a lot of people  and organizations still, today, no matter how open-minded and friendly they may be. aren't necessarily like that. So I think it's so  incredible and so wonderful that you all have sort of fostered this environment where  you know, as you've said, students can go and gain that meaningful experience to then gain  even more meaningful experience in their professional lives after graduation. I truly think that's.  you know, this program is something that's been the first of its kind that I've ever seen.  Whether or not that's true I don't know, but I'd like to think it is. it exactly. I know, at least for the Midwest. That's likely true. And I think that's something  that is truly just so  wonderful and impactful and  necessary.  because I think outside of that program, for you know.  regular internship experiences. I feel like it's really easy for disabled students to feel like  they can't go for those things, whereas  through this program  you're showing them, you can go for these things, and you can be successful at them. And while we're at it, we'll connect you to all of these other people that can help you get to different areas.  Should you want those opportunities. And I think that's huge.  So I mean props to all of you. It's it's really  amazing work that you do. And I know you're all very busy people.  and I'm I'm ultimately just very grateful for all of the work that you all put in. It definitely  does not go unnoticed by myself or really any of the other interns I would like to say.  you know, you all do very impactful and wonderful work, and I think it's really necessary. And I think you do a great job of it.  Thank you, Cameron. That's very kind of you to say, and I would  just added privilege for us to have you affiliated with our program, and I think you all can can see and hear why. Natalie, I think we are probably at our time limit.  Maybe if I could  ask you to take it and see if you need more questions for us.  we are. We started a little bit late, so I do want to give us just a few minutes for some questions, and I'm happy to pass the microphone to anyone in the room.  And those of you on chat, too. Please feel free to type in a question, and I'll pass the mic. Do you have a question in the back.  Cameron? I wrote down. I wrote down a question  earlier.  but you mentioned you mentioned that you had a positive experience during K through 12, and  when you.  When the excerpts, the the teacher made the modification for the pacers test.  I had a question if you had any positive exercise interventions while attending the university, and if so.  Were they challenging enough for you  to  improve your your physical abilities or your goals?  Thank you for that. I think that's a really great question.  Ultimately, I am not an athlete. I never have been an athlete.  so admittedly, I didn't really get involved with anything like that while I was in college.  that just wasn't something that I needed.  you know, degree requirement-wise.  and it just wasn't something that I had really thought about.  But I do think  with how the campus is set up. Being able to walk pretty much everywhere  was really beneficial.  I think that's something  that can be really easily taken for granted  in an area like this. Being able to walk, you know, to wherever you need to be, and not necessarily have to  rely on driving yourself around campus.  I think that's you know, huge  and I think especially because this is a bit of a smaller university campus. That makes it a bit easier to have that  But ultimately, outside of that, I didn't really have anything in college specifically  I wish I could give you a different answer. But that just wasn't something that I got into.  We have a question on Zoom from Bailey. How do we get in touch with the program to apply. Are there any certain deadlines? And is the program open to graduate students?  I guess this one's for me. So students apply for the program by the end of January every year, and as Cameron mentioned, the the staff of the Center then do interviews over zoom  with each applicant. We had 97 applicants this this year for for summer internships, which is awesome. And this university sent us the most applicants this year. So thank you. We recruit.  I mean word of mouth. But  the primary means for us in recruiting is working with each campus's Aes office.  Because those are the staff members who, for the most part, I guess Cameron, as an exception, know who the students with disabilities are who would qualify for our program.  So yeah, that's the application process. So we focus on summer internships.  because, you know, students are more available in the summer, we've got access to the housing in the summer. We do all the professional development in the summer, but having said that we do offer some fall and or spring internships, it's usually a much lower number. We had 63 in our summer program last year. We'll have 5 to 10 students intern with us in the fall and spring.  So  we do accept grad students. We've had several grad students in the program. So if you would be interested  in a fall internship with us, I would say, touch base with us  at some point.  You know, by the end of June, if you'd be interested in an internship next summer in in the larger cohort again, that application would come to us by the end of January.  Natalie, I might ask if you wouldn't mind sending out our contact information afterwards. Just so can follow up with any individual direct questions you might have for us.  Absolutely.  So, Larry, do you have a certain number of students that you accept yearly into the program.  No, we'll  so we'll try to find  an internship for as many students as we can. I mean, not. Everybody is ready for a professional internship. So of the 97 that applied, you know, after having a conversation with them.  you know, maybe 15 or so aren't quite ready. But, gosh! For the other 80  or so we're in the process. Now we're gonna try to try to make it work for as many different students as we can. And it's gonna be a good mix of on site internships, some remote. We'll even have a few students who are Ferrybach interns who are doing their internship  outside of Indianapolis. So Commons is one of our employer partners. Commons is headquartered in Columbus, Indiana. We'll have a ferry box center intern down in Columbus.  My old office in in Munsey, at ball State, the disability office. There is gonna host an intern from the program this summer. So  we're gonna try to bring as many people to Indianapolis as we can. But we only have a certain number of spots available in in housing and such. So there's a lot of logistics involved. But long answer Mercedes, to say that we're gonna try to  try to get as many as we can. I'm guessing. We'll have 70 or so in the program this summer. They're great great book. It's  the industry that knew those relationships, are they?  Yeah, that's such a great question. How do we connect with various industries and other partners? A lot of it's word of mouth. So Eli Lilly is is one of our strongest partners.  Lilly looks at us  to be their recruiter  for students with disabilities. Lily Yay sees disability as a critical piece of their Dei efforts, and  when when Lily came to us the said, How come? We don't see students with disabilities when we come to campus to recruit?  Well, oftentimes there's lots of barriers for students with disabilities, with typical recruiting efforts on campus career. Fairs are awful for lots of people.  especially for students with a variety of different types of disabilities. So a lot of its word of mouth. Lily has been such a great promoter of our program. Lily hosted a conference for other employers in the area. To introduce our program to them. And so that's how we got commons on board, and and some others as well. So word of mouth. And then some of it is  okay. We got an intern. This is what they want to do for an internship. We don't have somebody in that an employer who does that kind of thing? We'll go out and ask, we'll say, Hey, here's who we are. Here's what we do.  Would you mind hosting an intern. So a variety of different ways for us to get at at. The employers  want to be mindful and respectful of everyone's time. It's 11. 8. So let's end at 1110, and I think we have time for about one more question.  Anyone in the room or on Zoom.  Now there is a question in the chat about, do you have any fall internship opportunities?  Certainly, if if interested in fall, I would say, just touch base with us, maybe by the end of June. You know, for fall internships we don't provide housing. We don't do all the professional development, but our fall and spring internships are are the work, experience. The paid work experience. So we'll have 5 or so interns in the fall. So if you're interested.  Natalie will tell you how to get in touch with us. We'd love to have a conversation with you.  Well, let's have a round of applause for Cameron and Larry today.  We will be sending out a survey to all of those of you who've signed up on our sign-in sheet in our participating via Zoom. So please take the time to fill out the the survey. Additionally and we'll be sending a email with some information on how you can get in touch with Larry, if you have any further questions about interning with him and his team in the in the summer, fall or spring.  so thank you all and enjoy the rest of your day. We have another  event this afternoon. With our graduate students and professional students. Right here in this room at 10'clock, so please feel free to come back. Get some coffee and join us for discussion. Thank you.  Making yourself available  panels and conversation. That's better than the voices with disabilities program.

Zoom Recording of Fehribach Student Panel

Moderator: Larry Markel, Director of the Gregory S. Fehribach Center at Eskenazi Health

Panelist: Cameron Miller

IU Indianapolis Graduate & Professional School Panel

Intent: The intent of the Graduate and Professional Student Panel was to create a space for students to voice their experiences within the contexts of their graduate and professional programs, providing the campus community with an opportunity to consider how the academic experiences of disabled graduate and professional students are similar in some ways and necessarily different in other significant ways.

Impact: This panel highlighted the many ways in which accommodations may function differently for graduate and professional students, what these students see as the biggest challenges for disabled students navigating graduate and professional programs, and what they would like their instructors and the campus community to know about their experiences.

Description of the video:

See, okay, yep, and I'm gonna make my little unmute announcement anyway. Yeah, yep. Thank you. Alrighty. Okay, guys, try to get going. Alright, before we begin for those of you who are joining us on Zoom, please keep your microphones muted for the duration of this panel presentation, but feel free to type any questions you may have into the chat for the Q&A portion. Thank you for joining us today. The AES inaugural Disability Awareness Month is the beginning of our efforts toward creating a more outward facing and collective accessible educational community services. Educational services community of practice. The strategically brings existing relationships and services into collaboration to advocate for disabled students and students with disabilities to foster sense of belonging at IU, Indianapolis. I'm Elena Silverman. One of the accessibility specialists at AES and it is my pleasure to introduce your moderator for today's panel. Dr. Sanders Kouten is an accomplished professional serving as the director of operations for the Great Lakes Equity Center. They have for research, technical assistance, and educational resource development located within Indiana University's School of Education in Indianapolis. In addition to this pivotal role, Dr. Skeleton is also the director for the Region 3 Midwest and Plains Equity Assistant Center. One of 4 regional equity assistance centers funded by the United States Department of Education. Under title. My Roman numerals. For the 1964 civil rights act. Task of providing equity focus technical assistance to public pre K. Free through K 12 education systems across its expansive 13 state region. With a rich professional background spanning 28 years, Dr. Skeleton has cultivated experience in inclusive education, school improvement, and educational equity. She earned her PhD and Masters of Education in School Psychology from the University of Cincinnati. And holds a BS in psychology from Central Michigan University. In our current leadership capacity, Dr. Skeleton strategically plans, directs, and manages projects and services. Offered to state and local education agencies contributing significantly to the advancement of educational equity. Beyond her role at the Great Lakes Equity Center, Dr. Skeldon is actively involved in various boards and committees. Dedicated to improving education and life outcomes for minorized individuals. Dr. Skeleton's commitment to advancing equity and inclusivity is reflected in her numerous publications with representative works such as cultivating a positive ethnic racial disability identity and situating my positionality as a black woman with a disability. Dr. Skeleton's influence extends globally as she is regularly presents at state, regional, national and international conferences. Contributing to the ongoing dialogue and improving outcomes for marginalized youth. Dr. Skeleton, take it away. Thank you. Thank you, Elena. Thank you, AES. Program. Thank you for this wonderful opportunity. I wish I had this opportunity to listen to graduate students when I myself was going through my graduate program who share identities as I. And so I'm very honored to facilitate this esteemed panel. I'm going to actually pass the mic and have each panelist introduced themselves and when you do so to the extent that you feel comfortable, if you can also identify or share your identities. So in terms of your disability identity, I didn't need any other intersectional identities that you would like to share as well as well as the program that you're in. Anything that you would like to share that you would like this group to know a little bit more about you. So I'm gonna pass it over. Thank you so much. I am Mackanna Gilkerson. I am a 3 L. I'm in my last year at the law school. Hopefully graduating. I am actually the president of the newly founded Accessibility and Equity Student Union that was formed over at the law school. I'm very proud to say we have some pretty great membership and just being able like a doctor said we to see other people and relate to different individuals who identify the same as you and to communicate the different resources you all know. It's been so helpful and I won't go on. I know I'm just supposed to be introducing myself, but. That was just so wonderful to be able to experience I have Kind of 2 visible disabilities, one that, impairs motor movement, one that impairs mobility, and then my invisible is another one that I'm pairs mobility. And then I also have a mental anxiety disorder. So. Well, hello, my name is Katie Lipsius. I am a first year in the MDP HD program. I have multiple identities and I've spent a lot of time on this campus making a lot of friends. But, obviously the most visible of my disabilities is my functional and motor skills. Most people see it in my feet, but it actually affects my entire body, hands, mouth, speech, all of that. It's just less visible. And then I have other, you know, non visible disabilities, you know, learning. No, and then, you know, mental health changes, depression, stress. I'm a med student. Hello, my name is Claire Kobar. Stumps. I use them and she her, is pronounced. I, I actually also work for AES my third year and I'm a master of the school of social work. I'm in master of the school of social work. I'm in that program and my last year also hopefully graduating in May. And my disabilities are generalized anxiety disorder and ADHD. I am a queer non-binary person. I'm white, upper middle class. I'm white, upper middle class. Yeah, I don't know. Those were all the identities that came to my mind. So. Hello, my name is Ashley Woka Negative, but I go by Chachi. I use she her pronouns. I'm a first year in the clinical psychology PhD program, so I'm far from graduating. I am an immigrant. So I am a was born in Colombia came here when I was young so my educational experience is a little bit different. I have, well, I have a physical disability that I use a lot of mobility aids for. So in that in that way it's more visible because I use more AIDS. I use AFO, I use Walker, I use a cane, I use a wheelchair, I have various different. Mobility. AIDS that I use. On any given day. My I have a hyper mobility syndrome so every day looks a little bit different to me. So I might appear to not have a disability and then some days you see a lot more visible with me. I also have like various forms of like genetic disorders, bone issues, so various things going on, but from the appearance, mostly invisible if you didn't see my AIDS. Thank you. Thank you. While we're going to be doing that, pass the mic thing back and forth. So if you want to bear with us. I'm gonna kick us off with the questions not actually on my little list of questions. And the first question I would like for you all to respond to. And you all don't have to, but the extent that you would like is to what extent. Do you feel like you can show up as your full selves? And all of your identities in the spaces on campus and beyond. Who would like to take that one? That's a very poignant. I need a second to say. I I am also part of a protected class of white and upper middle class as was mentioned. I didn't mention that before so I do think I have a lot of protections going out but at the same time I definitely have found myself trying to. Mitigate my anxiety to order because people assume, oh, you're a woman. Oh, it's hormones. You can't be trusted long term with these kind of things. So when I when I was in college and completely undiagnosed that was definitely a big issue of trying to keep suppressing it until the point it actually boiled over. But that's another story. And then As far as. My mobility kind of. Disabilities that obviously one that's more, visible and one that most people don't know I have. I think we're kind of moving in a direction. I should have mentioned I've had my disabilities since I was born it's their congenital so just in the time I've grown up in 24 years, I've seen a lot of progress of people being more accustomed to seeing. Oh, that person's in a wheelchair. I don't need to stare at them. Oh, that person's using a prosthesis. I don't need to ask them what happened, you know, things like that. So I do definitely think progress is being made, but I definitely think there's some understanding that still needs to develop. And as for specifically on this campus, I've never really had any problematic encounters I can think of, so. So as far as me being a Hispanic woman on campus, I've never felt. On campus that I ever felt targeted or like persecuted in any ways. Originally when I did come to IUP, why I did have a lot of struggle with the buildings. I had issues with the elevators issues with being in the basement issues with my office. And I had to really fight individuals to try to get some works worked on, in my specific LD building. To get everything situated. And unfortunately, I had my wheelchair in my office and my wheelchair got damaged by maintenance staff and then I had to get it replaced. So I had a very unique experience here at IPY with my disability. However, so on the flip side. I did help to address some things, but everything was, it was very well received. When I did say, hey, my wheelchair has been damaged, my, the chair of my department immediately was like, we're gonna get this fixed. We're gonna get this replaced like there wasn't ever a question of, oh, like we may or may not do this or we might not fix this. Like it was always a dress in a very timely manner. Regardless it is difficult being a disabled woman on campus because it doesn't, you shouldn't have to fight. For accommodation. These things should already be put in place. So that was difficult. Like one day I went to the restaurant. I was locked in the restaurant because the button wouldn't work. And I don't have the strength. To push. Really hard. So that was a difficult experience and I was late to class a bit, be a graduate student like being late to class is really not something that you should be doing. But. As far as like how it was handled, I think it was handled in a timely way. It's just unfortunate that I even happen to begin with. But I feel like that's across the board. It's not only that IUPI that's in every location that you're at, you tend to have like those struggles. But I have very, I mean being in the social sciences, I feel like everyone on my department was like, no, we got to fix this. We gotta make this right. So I, I never felt that it wasn't going to be addressed or I wasn't going to be heard. It's kind of interesting, I think, that. A lot of presenting myself actually is self-imposed because my education here is the first time I accepted a formal accommodation. And I have 2 other degrees. Before this one. So. My accommodations currently are for ADHD. It has nothing to do with my physical limitations at all. And I'm so used to downplaying it and pushing past everything to show that I have the technical ability to do the things and move forward in my life that it honestly doesn't occur to me. That I need help until I need help. Actually the only reason and I will say this because I'm very impressed by it. I took accommodations is because one of the instructors in the anatomy lab because the anatomy lab is huge. Notice the way I walked and he was concerned that because of the structure of the practical, timed very quick walking around that I would not be able to make. Each like practical spot. And so he encouraged me. To go and reach out for accommodations that I otherwise would have completely ignored. Because I was used to doing so. But it is made a world of difference. But I still think personally I continue to downplay it. I think every time I tell when any of my classmates is, yeah, I gotta take the test earlier because I got accommodations. I'm pretty sure they think it's something to do with this. I don't know how because it's a written test but. But I'm not sure. But overall, I think It's mostly about me presenting myself as capable. And fully there and knowing somebody's gonna look at me and knowing the people are gonna wonder about me. Usually wrong. And do it anyway. And I'm so used to doing that that I'm usually not affected by it. Until I need the help, which I'm learning to do. Thank you. Thank you. Katherine, you was sharing your story. I was just. Reflecting on sheets just singing my song because that is that is I went through a lot of my graduate program is just not asking for help, not wanting to be perceived, is needing help. For fear of reinforcing stereotypes and assumption that people disabilities can't do And it's not until. You really need it and you always really need it, but it's not into the point where you almost do yourself harm. Do you do you then kind of reach out and so. I appreciate your story and all of you sharing. I want to sort of tag on this discussion around accommodations. And asking for accommodations versus I think trying to you what you shared is it should just be. Right, we should just be wishing have to ask. You know we're here in these spaces and these spaces should be set up where everyone feels supported and can and can do what they need to do in order to engage in the work and the studies and in their responsibilities. So with that, I'm gonna ask you, what would you like to share with your program or your department? And faculty as you think about implementing accommodations. Would you like for them to know? And if you would like to address both formal accommodations. But also informal. So who would like to take that question? I think this accommodation would be both formal. And informal, I think being in graduate school and having a disability. It's really hard to say, I can't do it today. Like just simply not being able to be productive and be present. In the classroom or on an assignment or something. Like just saying I need the day. I can't go to class. And even if I was to go to class, I won't pay attention or I'll be focusing on my pain, my ailments or anything else going on. Or even having like an extension for something that was do. I think sometimes it's really hard to ask for those things. Because we're all in such rigorous programs, right? Like you're you have the expectation that you need to keep up and everyone needs to. Like you can't fall behind and I think asking. For that time or that accommodation sometimes makes it feel like. Oh, I'm not. I'm not performing. I'm not. I'm not being the student that they want me to be. So I think Just allowing a student to say no. I have that I am saying this But I have a problem saying that half the time and I apologize in my emails constantly like I can't. Make it. I'm so sorry. Like today my wheelchair is being delivered, right? And I said, I'm so sorry. I might not be able to make a class because my wheelchair is getting delivered. It should just be I can't. Make it to class and I don't think that I should have to like provide. Information as to why especially if it's attached to like my disability. So I think that's something that Not just in my program, but in every program it should, it should be something across the board. Bye. So what what would you like your faculty your professors to say or do to create the space for you to feel like you don't have to explain yourself. What can they do? What can they say? I think Having that conversation maybe at the initial point of like the beginning of the semester would really help. Especially when you have such a visible disability, obviously if you have an invisible illness, like you have to really be very forward and talk to your professor, mentor, whatever that be. But if you have more of a physical disability, I think that it's like. It's very obvious that I might need some accommodations, right? But you either way if you express I have a disability I need some accommodations like having that initial conversation that beginning semester like saying hey. I sometimes can't do this and that way you just put that in the very beginning and then when you receive my email you'll see my text whatever the communication it may be. You understand that it might fall under that umbrella of. My illness won't allow me to do it today. But it's also difficult because you're, like I said, you're expected to perform and you want to perform and that's the hard thing too I think. As graduate students, we push ourselves a lot. Because we want to be present, we want to learn, we want to get engaged without all the information, but sometimes. Like our illness, our bodies won't allow us to. Know for me it was difficult at the beginning of semester because you're wanting to write notes so fast right my hands won't allow me to do it and then the sometimes the type to text doesn't work as properly or there's various different things that that go into the umbrella, right, that hinder your performance and your just wanting to keep up. So I think just having an initial conversation, a one on one meeting would be very helpful instead of just an email saying or forwarding an email saying here my accommodations for the semester like let's go that's like very quantitative data. Let's go into the qualitative data. Let's let's talk about like the the context that this is in, right? Like let's really have a discussion about it. And I think that'd be super helpful. Because if I explain it once, I don't have to keep explaining it. And I think that's the hardest thing is always having to explain yourself. And it just it makes it difficult to show up if you're always saying or apologizing for the way that you are. So I think based on my 3 years of working at AES and, being a student, I think I've been noticing a trend that some professors put all of the responses of providing accommodations on AES. And I think AES has great resources. I also think that informal, accommodations can be just as important. And so I think, if the professors, I think a lot of like all of them put them on the AES as a resource on syllabus which is great but I think if the professor could just open up and and say like if you need a accommodations that maybe AS isn't able to provide or maybe like be flexible like. Have some additional conversation outside of providing AES or resource because a lot of professors don't even know what kind of accommodations AES can provide. Also, what if you're not like able to get a diagnosis because that's so expensive. We live in a capitalist society, not, not everyone's able to afford that. So. Yeah, I just I and I also think that having those direct conversations with students will give professors more empathy for people with disabilities instead of just like doing like you were saying like the quantitative process I think qualitative is going to be really helpful and building connection and empathy with your students. So yeah. I'm gonna jump to the end of the question where you ask like what I would like to tell my faculty or my fellow students or those that are wishing to become medical students and so on and so forth. I think it's important for people to realize that they're all kinds of doctors. So all kinds of skill sets. So even if you may be limited in some capacity. It doesn't mean you should negate being a doctor altogether. There are several currently in some way shape or form disabled doctors. Who have informal or formal accommodations through whatever hospital or practice they work at that allows them to continue to practice. But there is a, I think an embedded stigma. That if you don't if you're not capable of doing everything you can't be a doctor. And it can be a little challenging. So as a person who has a spastic disorder, it means my muscles like to freeze up or constantly tense. When I type fast. I searched my muscles start to freeze. So the faster I type, more stiff my fingers get. However, there are requirements sometimes in classes and tests and whatnot where I'm timed. One half fast I can tell you to get my stuff in where all of my information is correct, but because I did not get it in because my hands pros. I get docked. And it's not even at this point the school's fault because I physically refuse to ask. Because I'm afraid of a response. And I'm not thinking that the school is going to No, absolutely not. You have you signed the technical standard. Good. No, I don't think they're gonna do that. I'm I'm afraid of seeing being seen as lesser than the other students that are capable of doing the things because it's just typing or it's just crouching the take, you know, petal pulses. Or any of the sorts of things that are just commonplace for people. It's not commonplace for me. I am not bendy flexible. My relaxed still feels very stiff to most people. And I have to work through that because I want to be a doctor who was seen as capable of doing all the things. Even if I'm not capable of doing all the things. And I think it's important because the medical school is fantastic. And focusing on student wellness. And student mental health and you know focusing on They know what's a stressful course. They know it's a stressful time. Also emphasizing that You can be a doctor. You might not be able to be a surgeon. I knock surgeon out immediately. Cause if I twitch at the wrong time, that's very bad. But there is an entire plethora more than I'm even aware of of specialties and fields and medicine that people are capable of doing. And I think that needs to be made more apparent. And yeah, that's what I'm gonna say about that. There are just 2 policies I kinda wanna apply or, yeah, address really quickly. I apologize if they're not widespread AES, cause again law school and different programs sometimes. One is the fact that many, accommodations cannot be requested retroactively. And I understand there are some things that just cannot be done if you have not made the school aware, but. One thing I know several people at the law school and I myself, we went into law school going, I want to prove myself, I want to show I'm just the same level as everyone. I took my own notes in college. I can take my own notes here. No, you cannot. The professor is talking and you pretty much need every word. So second semester, I approached my program and I said, hey, I know some several people in my class already requested note accommodations. Can I just have the notes from someone who know and I said, may I ask why? Because I just have the notes from someone who, can I just have the notes from someone who, no, and I said, may I ask why? Cause I have proof that I have the If there's an explanation, I can handle it like if it's not feasible, I can appreciate that, but just being told policy and I did not super great for the first semester material on those final exams. You know, that doesn't feel great. And then. One other thing again kind of regarding. How we present ourselves as people with disabilities. I the law school heavily relies on the student to reach out to professors for accommodations and like so many of them are very good about keeping that very private but even just them knowing sometimes makes you feel like, oh, they're gonna call me. Oh, they might not call me because they're afraid like you know it might be ridiculous it might not be true but it's still something happens and you know we we didn't all just wake up one morning and go oh I need to puff myself up we've experienced things that have made us put up these guards so it would be really nice if yes if we had the ability to talk to the professors if we wanted to but also to just be like hey can you you know not even tell them my name and just it when possible so those are just 2 things I would like the faculty to know. Thank you, McKenna. Couple of ideas or I take away from each of your sharing. One is that the idea of shifting the the burden in a sense of creating spaces where all people can. Be successful. Swam this from the student with a disability. To the system and to the faculty, right? So the notion that it shouldn't be up to the student to have to say. I need these things. What, what happened if we had faculty that created the space that opened up? At the start of the semester and offer. Here are some if you need some. Accommodations, formal accommodations here here's where you can go. And if you have a company the accommodations that may not necessarily fall under the umbrella of AES. We see me and we can talk through ways that we can create spaces and opportunities for you to be successful. You know, dismantle those barriers, right, and to be proactive. And the shift the burden from the student to the faculty another thing that I took away from each of your sharing is and particularly your sharing is representation. The representation matters. And the more that we see disabled people in different professions and different programs, in different spaces. The more that we can visualize that for ourselves. And move forward and to know The message is that anyone If you put in if you want to put into work. That you can accomplish the goals that you set for yourself if the barriers are dismantled for you to do so. And so this idea of representation is so important and to counter some of the messages. Because we think about medical school and law school and basically all of, you know, to counter some of the messages. Because we think about medical school and law school and basically all of, you know, the programs that you're in, you know, where we, where do we get a lot of our messages? And that's from television? And you know, what you see on TV is. The surgeon, you, what you see on Grace's anatomy, right? What you see in law school, right? And so how do we counter? How are those images and those messages? To create spaces and visions and ideas that are reflective of the diversity that we all have. Thank you so much for sharing. What you would like your faculty to know. I wanna move on to have you share a little bit more about your own personal journey. So personally reflecting on your journey as a graduate student or a professional. A professional student, what advice would you offer your past self in going to a time machine? As an undergraduate student or as a graduate student. Considering your identity. You're intersecting identities and specifically your identity as a student with a disability. So you're going back in the time machine. You're going to talk with your past self. What a bite would you give? And our day. I've been told. I have a problem of being too independent. Actually my mentors online watching this and he told me that. But various people in my life have told me that I put all of the burden on myself constantly. And then I'm like, oh, I need to fix it. I need to contact this person, this person, this person. But I don't seek support. That's the thing. Like I try to do it and I don't have any support backing me up. I don't tell people what's going on. I just act. And it's important to know that like everyday people have support. There's no reason why I shouldn't have that as well. And also find community because I find that At least in my program, I'm very, very fortunate to have. Many individuals in my program that do have a disability and we've talked about things and. I feel the representation in my department which Makes me feel good. It makes me feel seen. But even if I didn't have that, like find people find somebody that you can share your story with without, having that burden of feeling like, oh, I'm just complaining all the time. I'm a burden to others and so on and so forth. I think that I have a lot of, I feel like I have to explain myself constantly. Like one day I'll show up with a cane one day I'll show up with a wheelchair like I feel like it could be confusing to people and I put that on myself constantly like, oh, people are gonna wander, people are gonna judge me. And I think I would tell myself like, no, it's okay because that's how your body works and that you don't have to explain how your body works to anyone. So I just tell myself. To give myself some slack. That's the biggest thing like cut myself some slack. I think that especially being like a woman of color, I already have like some other burdens on me that I'm like I'm constantly facing. And being a woman of color and like in a very poor community like getting access to things was really difficult. Being Hispanic and being like you're tough you're strong like a Hispanic woman you're an immigrant all these things. And this like I've faced too much and I'm just like it's just another layer of things that I have to face. And I think that for me, I would tell myself it's Yes, it's okay to be strong, but it's okay to be weak. Because I go through so much and Disabilities hard enough and then you add various different layers and. Unfortunately it's not all like flowers. On the other side, right? Like you're gonna face crap and you're gonna have to deal with it and it's just okay to cry. It's okay to have a hard time. It's okay to ask for support. And it's okay to say no, that's a big thing like it's okay to say no. Oh, can you do this? I get invited to things and you're not physically able to but I push myself. No, it's okay to set no it's okay to set boundaries. So I think it's just important to communicate with yourself and be true to what your capabilities are. Be like tightly identify with your identities and make sure that you're being seen for your identities but not being like disregarded for them either. So. My advice to my younger self would probably be a immediately go to the Beatco learning center and get an academic success coach because that was fantastic. To avoid online classes at all costs. I don't know, yeah. My stuff is like practical, cause for me like ADHD, I can't do online classes. And then, continue going to therapy regardless because, that's just been so important. Me starting school, even as an undergraduate to me now, like it's light years difference because I, really had to work around and create routines and schedules for myself. And so yeah, just keep putting in the work and I did the work and ultimately be kind for yourself because like you were saying like things are gonna work out how they need to work out. And, you're doing the work and just to trust yourself and be nice. So. Yeah, there's a lot of things I would tell my younger self. But we have limited time. Okay, so I think it's really important if I could go back and tell myself a couple of things, it would be that my achievements academically, socially, whatever I achieved. Throw my academic career and you know, hopefully my medical one. It's not I did that. Because I'm disabled or I did that and I'm disabled they can be 2 different separate things. That you don't need to tag on. Katherine Lipsius is such an amazing inspiring person because she got a 4 point oh but also she's disabled. And I need to tell my younger self that I can do things without This as the forefront. That I can take a break. Because my achievements are already impressive enough that I don't need to do more to prove myself. And I think that was that would be extremely important to me and from a social aspect what she mentioned is like setting boundaries and saying no I'm not gonna go do this. I do the opposite. I do it like self-imposed. Like I have people from my cohort, thankfully, this very small, very close knit group. They'll invite me out to things. Yeah, Kate, you wanna walk to the student center or you want to go out and do this thing, want to meet up and I'm just like That's got walking. I don't want to walk and slow you all down because I walk slower than you all or I don't want to go try to do the thing because it looks really cool and then get there and realize I Probably can't do the thing. And then like, out the entire group. So I self impose isolation. Outside of any required academics. Because I don't want to be a burden to other people and that is important that I'm not a burden. To my younger self, over and over and over again. 2 things more? Except a cane? When you have bad days, I cannot tell you how my academic career has been stretched. So much longer because I injured myself. So dramatically that I am forced to take time off. Because I refuse to accept assistance. Because I was afraid to do so and for the love of God. Light in the backpack. Yeah, I definitely already have some back problems from law textbooks, so I'm sure you're right there with me. I'll try to make this quick because I'm really echoing what what's already been said. But my big 2 biggest things would be been said but my big 2 biggest things would be trust your judgment and don't judge yourself. But my big 2 biggest things would be trust your judgment and don't judge yourself too harshly, trust your judgment and don't judge yourself too harshly. I'll try to say a quick story. I have several examples of this, but, growing up whenever I was like on a field trip, touring a museum, walking around with friends, blah, I could not walk far distances and I was usually in pain after a short amount of time. And people were always like, Oh, honey, it's because you're missing a leg. You're okay. We're not, and I was like, okay, I know for a fact So what is it? And then kind of judging yourself. I was like, I guess I'm lazy. I guess I'm out of shape. So I would push myself and push myself and sorry I'm kind of into the mic but anyway and then My, the end of my first year of college. I fractured my ankle because it turns out I have a little bit of. Club foot, I think that's not the probably the not the proper medical term, but so my bone structure was weaker in my left foot and it eventually broke and that's what had been causing the pain for all these years. So here I will hear people were telling me what was wrong with me and I knew it wasn't that, but then I turned to just harshly judging myself and it was something, you know, completely different. So it's just. Know, know yourself. And don't assume that it's always the worst possible conclusion look to things to help yourself and don't just assume your You know, I don't know. I don't even know how to say it. You all said it better. So I'll end with that. No, this is great. Thank you so much for sharing. You know, it's allowing ourselves to be human. Right? And so amazing how, we hold ourselves to a higher standard than non disabled people. A hill too or hold themselves to because you're trying to prove not only to others but prove to ourselves and so what I would take away is echo, you, your, sentiments because I think a hundred percent. All, all the stories that you all. Have told I've experienced myself. And If I could sure encapsulate what you all are saying, it's just to tell your younger self to be human. To allow yourself to be human, to allow yourself to show up. And the human experience in the package that you're in. And be okay with it. In the be okay with it. Thank you so much for sharing what you would say to your 25 year old stuff or however you are back in in undergraduate school. I am going to go to our, do we have time? Okay, so I'm going to go to a concept after question around a concept that have come up a couple of times and you're sharing. This is the concept of intersectionality. So intersectionality is the experience is experiencing overlapping and compounding systems of oppression. Because you may embody. Multiple minority or marginalized identities. And so we all have intersecting the identities, each and every one of us. We're all more than one thing. One more than one social identity. Some of us and body identities that are modulized. In our current society. And some of us. Embody multiple identities that are marginalized. Every single person is panel. And body, intersecting, marginalized identity. So every person in this panel have experienced navigating and intersectionality. So I'm just gonna pass, I'm gonna ask the question and then just pass the mic. How has been a graduate or professional student? With the disability influenced. Your perspective on intersectionality. Particularly within your programs. So how as your how it's been? I graduate student or professional student. With a disability influenced your perspective on intersectionality. Particularly within your program. Oh, I guess I'm starting. Particularly within my program. While I'm the only person of color in my cohort. The only person of a color like student wise in my lab. There's really not a lot of Women of color in my and as faculty there's maybe like 2 and. Like I'm the only individual that uses AIDS like mobility aids in my department. So I think that there's a lot of overlap in the way that I think that I present myself in the program. I think it's difficult to say things I want to be addressed. In the program. Sometimes I bite my TA little bit, cause there might be an issue of, religiosity or race or disability. And I tend to be like that warrior to want to like always speak out about that. But it kind of sounds like I'm a broken record if I keep going forth on those topics. So I think that's really difficult for me. Because I become that annoying girl that only wants to talk about these things even though they're super important things. Obviously the field of psychology is a little bit more difficult since we're talking about that constantly but we're not where we need to be as a people. We're really not. So I think it's really difficult for me in the program and just in school in general to keep voicing my concerns. And keep voicing like this isn't right we shouldn't do it this way maybe we should adopt the way that we think would adapt the way that we approach things. My program did a like pre school kind of a DEI session, right? And it was really difficult for me to be in that DEI session because it felt very forced. It didn't feel very intentional. It in myself being I always call myself a melting pot of identities because I identify with a lot of marginalized and in minoritized communities, right? It's really hard for me to be the person like We chose an exercise that required a lot of mobility. That's not the spirit of DI, right? There was just a lot of issues and I'm like, we can address these better. So I tend to find myself biting my tongue a lot. Trying hard to say what I want to say with a lot of intentionality and be really focused and honed in. And really speak when I really need to say something. But it's difficult. I came from Dallas, Texas, like originally, right? And Dallas, it's full of Hispanic people. Absolutely, like you don't see white people at all, right? And then coming here and like I'm the only Hispanic person in my, like in my community where I live at school. I'm the only Latin woman in my department. Yeah, Latin woman in my department. So it's just, it's just hard to like be yourself and like try to find home. In somewhere that is at home, right? So there's a lot of overlap in that. But programs like the AES Center and stuff and have really helped me. But like I said, we as a people have very far to go still, so it's kind of hard to adjust those things. I, as someone that's like really involved in the queer and trans community, I think the queer community has done a great job of in bracing disabled folks and people with disabilities. So I think that has helped me embrace my own disability a lot more. So I feel very fortunate to have a community like that. That's so supportive. Of people with disabilities on top of that I also know that I'm like But the only reason I've been able to make it this far in school is because of how privileged I am. I'm a 5 29 baby. I, I've been in therapy since 13 so my parents have been paying for their and I'm 22 now so they've been pairing for my therapy this entire time. They've been paying for my medication. And yeah, yeah, so it's, and it's also not lost on me that 3 of the 4 panelists up here are white. So. I think. It. In the school of social work, there is a lot more, diversity. So that's been nice to have in classrooms as well to like, you know, have different perspectives. But yeah, I think that's that's the main thing is just like realizing, but yeah, I think that's, that's the main thing is just like realizing, my privilege and doing what I can, to dismantle that so that you don't have to have privilege and doing what I can to dismantle that so that you don't have to have privilege to be able to, be able to dismantle that so that you don't have to have privilege to be able to be a graduate student. So, yeah. I think I kind of take the fact that people are already looking at me. As the excuse to open my mouth and say something. Because they're already looking at me. They're already expecting me to explain something or, you know, do something like a magic trick or something that explains why I'm walking the way I am or some people would just come up. What's going on down there? I've had that happen a lot. And so it gives me an opportunity to speak out for people that might not be comfortable speaking out. I've got a lot of people that will come to me because they know me, they know my experiences, they know. I'm originally from Maryland. I came from Cambridge, Maryland, a very tiny town on the eastern shore of Maryland and nobody ever heard of. We're not on the Baltimore side, okay? On other side. The farming town, fishing town, so. Very small town and you've got a very obviously disabled child. Very poor family struggle to grow up and now I'm currently You know, financial support and, you know. Just a general social support for my family because my mother severely disabled so I've kind of taken the matriarch role at like 29. Though I'm sure she'll disagree with that if she saw this. So I'm used to having to kind of straighten my back and say what needs to be said even if it makes me horrendously uncomfortable. Because it can make a difference as long as it's out there because half the time people just aren't aware. Of how There it is not malicious, but how ignorant they can sound when they say things. They're just curious or they want to help or they don't know how to help so they approach. And you know, try to ask questions and there's the right way to do it and there's a wrong way to do it. And you can usually tell because all of this has gone through this multiple times. When they mean it in a malicious way. And then that's another story, but I think. Being a person that's always been, you know, looked at in small towns. So every time I did something amazing. I was in the newspaper. I love you Cambridge. I'm not making fun of you over When people come up to me and go, you're amazing. I'm like, you know what else is. Social services, food stamps, help the people. Do you recognize that the very underverse population of medical students here. Work it in there some way a lot nicer little less blunt. But no, I try to use it even if it makes me uncomfortable because I am privileged. I'm very noticeably disabled, but I am very white. I'm like as void as you can get. I'm more translucent now. But it means unfortunately or fortunately that people tend to listen to me a little bit more. So if I have to be a mouthpiece. Gonna be a mouthpiece. Yeah, listening to my fellow panelists has really, given me some self-reflection. Besides being the president of the accessibility and equity student union, I don't really know that I really. Embrace my intersectionality. I, you know, now that I'm thinking about it, I think I really take the the privilege classes that I'm part of white upper middle class so on and so forth and. That's just sort of what I've leaned into and made my personality. So I appreciate listening to you all. It's been very, very, thought provoking. Connected with that. If you can reflect on. How you would either support in the world, individuals to be allies. And I can even go so far as to say accomplices. And dismantling, ableism. Racism, sexism, classism. Hello, Sexism. And the intersection of all of these. I, oppression systems of oppression. What would you either say to a colleague? To support their allyship and accomplish role or how would you yourself? Appolate as an ally. For individuals who may not embody the same kinds of privileged identities that you embody. I'll give Chachi a break. I'll start. I largely rely on encouraging one self education because you know as was said when you have a visible disability people expect you to be that education source and that like we mentioned earlier that responsibility shouldn't necessarily have to fall on me. So self-education and then I definitely think visual representation is so well any kind of representation is so important as again was mentioned because There are a lot of people like I don't I follow a lot of I guess influencers with this abilities and it's just really upsetting to go into the comment section and see why should the whole world have to accommodate your one need or you know why do you have to do that like this poor woman was trying to shop for clothes and people were saying this and I just think if we can put ourselves or put people like us in front of them to gain a little empathy from the public. We'll start to see sort of like, oh, okay, I guess, you know, making these accommodations so they can live their lives because they are in fact human beings might be something we can actually manage. So education and visualization is just the 2 things I push. I'm just gonna echo that self education is extremely important. In a lot of marginalized and underrepresented communities. They get the same thing. That we get, they're expected to explain everything. But phones are internet now, so. Yeah, no excuse. To not want to Google something and then if you have specific questions you know maybe we can help you out. But I also think When you mentioned empathy, I think it's kind of hilarious because if you sat down and asked somebody where they think they're gonna be. In 50 years. Everybody is only temporarily able-bodied. So eventually you don't want to climb those stairs or eventually having a rug on the floor is going to trip you up and eventually you'd like if your grandchildren would just slow down a bit so you can catch up before them. So you're temporarily able-bodied. But that doesn't apply to you now. So it doesn't matter now. And I know people. Are good at heart and trying. And I know it's kind of confusing on how they think, like you said, why should the entire world change? It's not the entire world. It's small and minute changes that you all don't even notice. That make our lives so much easier and then encouragement finding people that are in your cohort or people in your community that have the same identities as you that share something with you and acting as that role model standing up and having that courage. So hopefully they have that courage there too so they can also become visible and no longer kind of hide away thinking that they need to. I, yeah, to echo, Self education is great. I would also like to couple that with community organizing because these are systems of power and they were put in place to marginalize people. It's not just people with disabilities. It's also people of different races, you know, the whole gamut, people of certain genders. So yeah, community organizing, people aren't just gonna wanna be able to fork over the power they have. They're benefiting from it. So, yeah, self education coupled with. Community organizing, get active in community mutual aid. Mutual aid is one of the biggest powerful, most powerful things you can do for people with disabilities. If you're unfamiliar, I recommend reading Dean Spades book. so yeah, and like how you're talking about like. We're all in community with people. People you love, you yourself are going to become, have disabilities at 1 point or another. So just like learning what that means and how you can accommodate that. Also read books when you're self educating read books by people that have disabilities like those authors. I recommend Alice Wong. She's fantastic. But yeah. So those are some of my So. Just to like highlight the question, it's like, ableism, racism, like homophobia, whatever it is, right? I'm in the unique position, but like I said, that I fall into many of these categories. I've experienced all of them and while this is not taking the lens of like how others can shape it and taking the lens of how I can shape it. As a person that's experienced all these things. I don't fault people for individual actions. So say somebody. Says something that's very like racist towards me. I don't take the stance like I hate you. I'm going to push you out of my life. Like you're the worst. I always take the stance of I'm gonna show you kindness. Because these are these are things that people do wrong, right? The way that I react can possibly only prove them right. And I don't fault people for individual things. I try to help them see. Like, this isn't right. And then let's try to bridge that relationship and make a better relationship between the 2 of us. Like I've been told like wet back to my face like various different things and instead of being like you know what you don't know where I come from I'm just like how would you feel if I said the inverse to you like Wipe like this was native land. It wasn't that it wasn't necessarily like filled with Europeans at 1 point in time, right? So I always try to. Help address it in like the kindest way possible because I feel like that addresses it more so than if I meet it with hatred as well. Which I think is something really hard for me to do and anyone that's like a minorized group to do because we again we take that burden on ourselves yet again. But I think sometimes that's the best way to show and reflect to other people like we can change the way that we think we could change the way that we act towards others. So that's been the way that I've addressed it. Well, sometimes you can't convince somebody you can't, you can't push through with somebody you can't convince them otherwise or something that they think, right? You can at least plant a seed that maybe this isn't the best way for something for you to communicate it or any way shape and form as far as like institutional like let's say the university. I think that these spaces weren't created with like us in mind. Which is it's a hard thing to, to think about, right? So like IUPY, I mean, or IUI, sorry. In particular was made like as a commuter university, right? So a lot of the facilities weren't made. With individuals with disability in mind. So it was quite literally not built with us in mind. And I try to take that and take consideration like not everything is going to move at a pace that you want it to move. But as long as like you can push it in a direction or like voice it and help others go in that direction. That's the best thing that you can do. And not take the burden on completely yourself because I feel like sometimes I'm like I'm gonna do this I'm gonna accomplish it. There's not necessarily, it's not like about the end goals about the journey, like getting people to make the right actions and getting things to. Getting people to see like, oh, maybe this wasn't the best way to format the building or maybe this wasn't the best way to give a accommodations to this individual. Like planting those seeds will in turn Impact others, not just like yourself, right? It'll impact the way that they address it with other people. It impact the way that somebody else's experience at the university will be. So I think just My biggest point is just planting seeds. Like it's not, doesn't sound big. Like it's very small actions, but it could lead to very big change in my opinion. Well, I was I was just gonna say that we're, or about out of time, but I want, so I want to be respectful of all the panelists time and Dr. Skeleton's time. But I also wanna just ask if there are any, if you guys are willing brief questions. If you're on zoom you can type into the chat the questions you guys good to take a few? Okay. Yes, Elaine has been working with me for probably last 18 months or so. Before that she had another colleague that's now transferred to Columbus. I've come back to school since. 2018 and ran into some difficulties. I asked a lot of questions for service between AES, cats. And I was not getting very, very much. Cooperation. My name is Mike Brown. I'm sorry I didn't throughout to introduce myself, apologize about that. I'm not a very good public speaker. But I'm an older student returning. Came through, started here in 1981. Dropped out in 1986 was taking part time night classes. Had no direction on where I was going to go with life. And I got issues dating back age 13 and 1975. I was first diagnosed with. And the second issues that I've had all my life and wasn't diagnosed with until 2,008. I struggle with because I didn't know I had it. So I was tested by both rehab. And FSSA. And services hasn't been too great with the help of them either through FSSA or work one here in Marion County and so forth and so on. And. I have a skill set. I didn't know I had because I started back to I. In 2,009. I didn't learn it at first I got a degree in business. That was in supply chain logistics management. When the light bulb went off, it was 53 years old. Discovered what my natural skill sets are for being. What I have the first thing it's lend me from getting into jobs or physically nothing wrong with me it's all hidden. And unless I disclose it. First was epilepsy in 1975 when I was 13 years old. I've been on MED for that ever since, almost more than 48 and a half years. Sees her free for 37, but I'll be on meds the rest of my life for it so I can drive a car. And then it wasn't until 2,008 that Vokery had had me tested. Band out that I've had spectrum disorder, learning in certain circumstance not all my disciplines of learning but certain disciplines of learning I've had struggle with going all way back to grade school. I started out here in pre business. Try to get in with Kelly. Cause I got, not only in the 2 degrees, that I be taking business in supply chain. But discovered my skill set being in 6 Sigma. So I got my lean and white belt certifications right off the bat, knocked them out, wanting to get my green belt. But then I got shut out by for circumstances there that still unexplainable. And then I also got a machinist certificate at IV Tech in 2,000 when I was 38. And then I would hire me because I had no on the job experience even though I had a 3 point. 8 5 GPA. In that semester or class that we took, I was working on a day job and taking 16 credit ours for this. Whole semester and nobody would hire me, you know, certified for CNC, both mill and laid and so forth and so on. Applied to 100 different places and I would take So I've had trouble holding on to jobs. I've worked for the state. I've worked in retail. Not that I'm not doing my job. I showed up every day. I worked my rear end off. I didn't have a lot of these disabilities like I said until I was 48. Not in a structured K through 12 experience. I'm the oldest of 4. My dad was an industrial management. So he got transferred quite a bit so I went to 5 grade schools, 3 high schools, 6 different states, 7 different states. So she's real aware of what my circumstances are because we talked about it. So my question is, I apologize for telling my life story there, but. I got into. Starting asking questions. I was trying to get accommodations here and so forth and so on getting some tutoring and so forth, on certain subcales struggling in statistics. My county, that type of thing, which would raise my GPA. And there was no assistance at all at IV Tech when I was going through school at that timeline in 2,009 and 2,016. I'll be 62 next month. And I got forced in after being in Kelly for one or 2 semesters. I got transferred into. Little arts general studies, which I'm not having been happy about. Let me, there would be employers. Goodning on me once I have graduated, I had my killer degree in supply chain logistics management. Well, I'm not too certain about my future. With a little arcs, panel studies degree. So my question is, is there anything that I can do? Because I plan, I have nothing, technically 5 years to retirement. I'm like to work climb 73 to 75 years of age. In order to have enough money safe retirement if I can get into my field of services. I'm trying to get into. They've never made more than $30,000 a year in my lifetime for calendar years. So I got nothing saved up, nothing. So I'm basically broke. What can you do? Cause I contacted the Great Lakes people back in 2,021. Contacted the higher learning commission here in Indiana. Also on 2021 None of them seem to want to help me at all with my situations. So I don't know what to do and. So forth and so on. So I didn't know if you know anybody can help me out with this and so forth and so on. I'm gonna have to take some grad classes. Don't know which ones to take, but I was forced out by the powers of this university. And because I, such a concern back in late 2021. They banned me from campus. The entire academic year, 2022. In the spring of 23. And so it's even the people of university that run universities, the pack that from the Chancellor's office. And down through AES and so forth. It's not her fault. It's previous administration. It was with that she took the place of. And so I'm just questioning what can I possibly do? Or what's gonna happen to me for my future is what I'm talking about. I just want to say as AES director that Michael, I've been knowing you for quite some time and thank you for being very transparent and open with, with us today. You are talking about some really embedded, ingrained types of system things that happen, right? Sorry that your experiences have been what they are. And I'm not quite sure. If the panelists would like to say anything, but if they do want to, they can. And again, thank you for your transparency. At this time and we'll get responses from folks if they have it. If not, then we did hear you, Mike. We're supporting you as much as we possibly can. As an office and thanks for Elena being able to work with you and Yeah, so I'm gonna stop there because I think that you spoke very boldly and clearly exactly what you have been experiencing. And I do wish you all the best. And wherever you go from here. So Sina wants to speak. I just wanna echo, thank you for sharing your story. Unfortunately, it's a story that can be told by many. The systems are not set up to support. People and there are barriers that are in place and obstacles that those of us who have disabilities and other identities have to navigate. And it's hard to find those systems of support. I appreciate you reaching out to the great waste equity center. Our center works. With public K 12 education systems. So that's why probably. Yeah, yeah. And in our center. Yeah. And I said it wasn't, didn't come into existence until 2011, 2,011. But what I, what I can say is that to leverage the support that you're able to connect with. You're working with AES? I'm assuming to continue to leverage those supports the best that you can to continue to tell your story to reach out. To try to connect with others who may be dealing with similar kinds of issues. They may have strategies that that they can share. And I thank you for sharing, sharing a story and I'm sorry. That you have had to deal with these kinds of issues. All of your life and. Unfortunately These are the stories that we hear a lot. Yeah. Sure. Yeah. Yeah. To get out of. That. Very good. So that will be back a lot of. You call an old student. 68. Some of the Okay. Right. In the middle, Right, right. That's, you will, and support certain categories. Oh, You've met that way. Okay. And, and, we'll see, So They didn't have a One Thank you. Thank you for sharing. Thanks, Michael. We have a question from one of the online attendees, AQ. I believe this question is for you, Claire. I'm glad you experienced diversity in the school of social work. I did not have the same experience unfortunately. Is this something that you have heard from others too or is this your own personal experience? I guess I would say diversity relative to the rest of. UPI in Indiana I would like, I guess I was comparing it to my other classes. Just because social work draws people with lived experience of some really tough stuff, people get in it for personal connections and typically that's people that have been marginalized in some way by society. So I'd say that personal experience. I've had discussions with other people have also said, so that was my bachelors of social work. At IA little bit less in the masters. But that's personal. So I'm sorry you didn't have that same experience though that, sucks to not have that representation for sure. Anybody else questions? From the room, from the online audience. Alright, well we have actually gone over our time by about 15 min. So thank you to the panelists for being willing to stay around and Dr. Skeleton as well. Thank you. Thank you. Thank you. So much everybody. Was wonderful. Thank you for those of you who joined us online. Oh, I'm sorry. For everybody in attendance, there is a quick survey. It is linked on the QR code on the handout that's on the tables sort of randomly. For those of you online we will send it to you via email. So thank you very much. And we'll send it to you again anyway because we really need to see that. Okay. So, you know, they'll get a, maybe a couple of times. But yeah, thank you so much. Oh

Zoom Recording of Graduate and Professional School Panel Event

Moderator: Dr. Seena Skelton, Director of Operations for the Great Lakes Equity Center in IU's School of Education

Panelists: MacAna Gilkerson, Ashley Bocanegra, Katherine Lipsius, and Claire Kilbarger-Stumpf

Mini-Resource Fair Event

Intent: The intent of the Mini Resource Fair was to increase awareness of the variety of resources and offices that support increasing access and opportunity for disabled students at IU Indianapolis.

Impact: It gave students the opportunity to connect with campus partners that work closely with AES, while also allowing the offices to network with each other.

View of the Multicultural Center table where representative speaks to attendee holding a brochure
View of the Mental Health representative mid discussion with an attendee
view of the resource fair with tables set up and attendees speaking to different resource representatives

Beyond Awareness: IU Indianapolis Assistive Technology Demonstration

Intent: AES’s collaboration with the Assistive Technology and Accessibility Centers (ATAC) aims to foster a vibrant community of practice among the students, faculty, and staff we work alongside daily. By engaging in educational sessions led by ATAC staff—such as accessibility analyst Tomas Gregg's recent demonstration on assistive technology options—we seek to nurture our partnership with ATAC. This initiative deepens our understanding and application of inclusive practices while supporting ATAC’s work of ensuring a diverse range of services, resources, and support are available across all IU campuses.

Impact: This initiative extends beyond mere awareness of disabilities; it cultivates an environment where all members of the IU Indianapolis community can collaboratively explore, implement, and benefit from enhanced accessibility. We see the value of individual empowerment and contributions, leading to a more inclusive and supportive academic experience.

Description of the video:

That's good to do. Sorry, we had to start the recording. So for instructors, it helps them and it grades them. On how good their content is and how they can fix it. And it also walks them through how they can fix it. So it gives them feedback. And instructions. For the end user, the students. Everybody in your students or does anybody? Is that? Or anybody who takes courses that are offered through Canvas. What Allies going to do from the end user side is it lets you digest that content in different formats. So if you go to a Canvas page that has like. 5 pages of text and it's really long. You're like, man, that would be great if I could just listen to it on the go. They have a feature that lets you do that. It's baked right in. So I have this Canvas page up here to show you, cause we've got a page. That's all this tagged in it. So if you wanted to be more mobile with it. There's this little A icon with a down arrow to the right of the title. And if I click on that or I activate it, it props up this down alternate formats menu. And from here, oh, I want this as a. Audio MP 3 file I can throw it on my smartphone or other device and listen to it on the go. Where you can have it as an audio file if you wanted it as we'll be talking about a Mercer breeder later in format it so it reads per Mercer. This is a PowerPoint that you would like it as a PDF. Those types of things. So it gives you as the end you a lot of confirming how you want to digest your course content. That's doing it from, you know, oh, that's the whole page, but the other thing that you get a lot in Canvas is things that are actual files that you have to download. These could be work documents. These could be PowerPoints. So another page example. And so we have lots of different examples on this page. Notice that there's that little to the right of the hyperlink. There's 1 icon that kind of looks like a downward arrow that's like kind of crushing a little line down. That's our download option. From it, you'll see there's all that alternate format options again. So even for those files, like I mentioned, we can go in here to this Word document. It's because I'm doing this special view. It's not being, but we see that we have all the different options. From here. So just like the document, the Canvas pages. Our file attachments can also be converted into altern. So that's a little bit about the ally alternate formats. Does anybody have any questions about that? And fairly straightforward. Okay. So what happens from the from the faculty side? When they develop their doors and they upload it into canvas. When they first develop a, initially get scanned, but anytime that they make changes to their course, LA goes in and actually scans the course again. Thank you. Notice that a, for example, word document. The instructor didn't put headings inside the work document. So somebody, reiterated a user doesn't have an easy way to navigate the content. It's gonna get, matter of fact, I can show you if I leave this student here. Students never see this view. That's why you never see these, but you see these little dials. These little things off to the side. And this is for the instructors only. Never see these as a student. These tell the instructor. How well that document is. So I've got some here that are red. So, can click on that. Tell you what the score is, tells you what the issue is. And then it tells you how to fix it. It will walk you through the steps of how to fix it. So it's gonna help guide that instructor. On how to make their content more accessible. Okay. They don't for sometimes it's like it's a heavy lift, right? You tell a structure, oh make this accessible. So the allies just kind of guide them along the path towards making. Thank you. Any other questions? I'm gonna go back to that page that had a lot of text here for a second because this is a good example. Oh, how many people in this room if you knew that there were technologies that could read your course materials back to you? Find that helpful. And hands up. Okay, I know for the folks on that I can't see them so. Like chime in the chat if you want to. So. This one is built both into the. Does operating system but also if you use any of the office tools well not all of them but certain subsets of office tools. And a Mercer built into it. So in this example, I'm using Microsoft Edge because that's the browser that's built in with Windows. In the address bar. 2 icons for reading. There's this one that looks like a little A with 2 little wings tied off to the side of it. And then we have an icon to the right of it, which looks like a little open book icon. Speaker with little sound waves. That is what's called immersive reader. Yeah, I'm mercy for your stand do more than just the reading. Go ahead and launch it here. Did you see it totally reformatted the tags? It stripped out everything it didn't need to accept the main content so we don't get distracted by other things. And then we have some options in here. If I just wanna have it read that. Or 6. I know what I forgot to do. We have to share the audio from my session so that people in the room can actually hear it. 1 s. These are Etexts or digital versions of physical textbooks and other print materials are presented on the university standard, feature rich, and engagement promoting eer, in Gage. Look for a link in the main menu of your canvas site label. You know, and. Like it to open your engage bookshelf. Okay. So. It's actually reading it's really soft right now, but there's a synthetic voice that's actually. See the engaged tutorials to learn more. I'll exit that because we have some other settings in here. So you don't like the tech size, so you need to maybe boost it a little. A slider for that. You can increase that. Okay, the characters are too close together. So we can actually, in and it stretches it out. So maybe for some people, this is, and it stretches it out. So maybe for some people, this is helpful for them to be able to read the text. Access to different. Once we can just how wide the text looks. And if you're somebody were. Backgrounds are too intense for your eyes. They have different, so we can switch the contrast and maybe move down a little bit. Well. The thing that's cool is Teacher called line focus. So. Here. And all this text, right? It'd be great while it's reading it if we could only just kind of focus more on a smaller subset of the page. That's what blind focus is designed to do. Where it actually kind of walks and hides the other content so it's not as visible. I can stay on track visually as I'm falling along with the reading. If one lines too intense, I can get 3, I can go to 5. Have that. As it's reading a particular area. Not from here. Let's just showing that area as it's kind of reading along. You must open each title for the first time in the original Canvas class site in order to authenticate your access to the title. So this is web content, right? It has a Mercer, built into Word. You're writing a word document. You want to have it read back to you just kind of get, this is a sound right to me. I can use this in Word. And you're composing a new message in Outlook. Built into Outlook. Doing notes in Onenote. You're doing the fields and PowerPoint. There's different, there's a whole different suite of areas that they have a mercerator. Ecosystem. Something that you have access to and Mike said you could just walk out today and start using it. Any questions about immersive reader? Whether in class or online. Well, that we PDF. Okay, so separate tool for that. And what's nice if the PDF. Has underlying text in it. So. As anybody ever opened a. Yes, an acrobat and when you click on the page it like highlights the whole thing in blue. Yes Okay, we know that's that's an image PDF. There's no text. So if you have one of those. The with the PDF reader in edge, it won't do anything with it initially. If it does have the underlying text, you can little just drag the PDF in the edge. Inside of it and have it start reading it back to you. Also assuming that the underlying text is actually proper because somebody did a bad job. In the optical character recognition, it can gibberish and then what it's reading. It doesn't make sense at all. So. We're gonna switch gears a little bit. So this was having it read content to you. Oh, I'm gonna present the opposite now. Wouldn't it be nice if you could be talked to your either? For you That could be gibberish too. Okay, so. We're gonna start with what we what we would traditionally use as a more basic one. So. Switch. So let's go into, I mentioned there's 1 called Microsoft. 3 65 dictate. And so this one is built into. Several office tools we have access to this and word you will have access to this. And Outlook, you will have access to this in Onenote. So the PowerPoint as well. What's nice is that This technology doesn't require any. Training you literally just turn it on and start using it. I don't know if anybody has ever played with this dictate button inward or ever seen this before. So and pay attention to it. So I'll be curious with the mic in the room how well it does. We will see. Hopefully if this picks up my voice. We'll start typing. The word. So I will have to do this for a second. No. You. Okay. So let's just try talking for a few seconds. See how well it does dictating into Microsoft or period. Not listening. Yeah. So just like that I could just hit a microphone. Yes, sir. Yeah, this is something that you can use. Right in London. But read it back to you like if you're visually impaired. We want to know what you just said. Correctly. Screen leader user. Somebody who uses like jaws and VDA, those types of tools. You would be just navigating your Word document like normal and it would read it back to you. Got it. If you're somebody has some usable vision or somebody else's, that's when you can switch over to using immersive reader. Have it read back to you. Do you have like a Hephones would might. So this that's a good question. So. It's recommended that you have a headset. That's coming off you the best experience. So it would also work with. 2. When I've done demos of this, like there's a tech fair that goes throughout the new campuses throughout the year. Sometimes I don't have my headset, I just have a webcam that's on top of the monitor that I'm demoing on. I've talked through that and it's worked amazingly well. Yeah, so what's in with the software again? So this is called it's if you looked at the Microsoft site it's the rules called dictate. They call Microsoft 3 65 dictate because it's part of the 3 65 suite I believe it's also, so we're talking desktop as well as I've used it like on my in that version of Word. Obviously, and you have the built in option on those devices as well. But yeah, it's the especially if you get this like I'm gonna talk about the next tool here in a second and having a headset's really important because. You're not using a headset, you're using whatever's built into your. Might be great for doing. Like teleconferencing, zoom, that kind of stuff. But, may not be the best for doing what would be. So if you, what I would say is try what you have. You find that the experience is. Very good. You kinda laugh at it really badly. Then you would probably want to invest in a headset. I will be sharing information about that later too, so I promise. Give you some options in terms of if you want to go down that route. Any other questions about and I this is like a really quick introduction to dictate though The next one I'm going to show is we're going to amp it up a little bit more. Oh, this is, and they take can do some. Editing and stuff like that, but you're stuck in the Microsoft ecosystem if you do. We need to do something. And a web browser or some other. Application on your computer where you type. Thank you. Not the solution. The other thing to remember about dictate and I did not mention this is that Good. Processing is actually not done on your computer. It's done in Microsoft Cloud. So it requires internet access to use Dictate. That's something to keep in mind if you try to, if you don't, if you're somewhere where you don't have internet, and you try to hit that dictate button, you're gonna get an error message. Keep that in mind as wherever you have internet access. Dictate feature. Now the next tool. Is what we call voice access. Now, a lot of the demos today are heavily on the window side, but if anybody, I can switch over at some point to show you Mac solutions as well. That's what I have up here and I live in both. Okay. So like for this one, I'm gonna talk about voice access. If you had to do the equivalent on the Mac side. It's built into mac OS. It's called voice control. What's nice about voice access is it gives us that flexibility. So we're not only just being able to talk out our thoughts. Wanna edit. We wanna fix things. We want to launch applications and browse the web and do all stuff just like talking to our computer. That's what voice access going on was to do. Let's close this just for a second. So the thing to remember with this tool, voice access is It's only available on Windows, 11, so if you're on Windows 10 or earlier. One have access to voice access, but you do have an option called Windows speech recognition. Built right into your Windows computer. Type in Windows and you start types beef, you'll see it come up with a little microphone. I find you can access that. Yeah, on Windows, 11. There's a caveat within 2. You have to be on a certain update of Windows 11 to have. Now if you've had a Windows 11 machine within the last 2 years. Probably on this. Version. The build. If you ever need to find this out. You're start if you're right click on it. System. Architectural right menu. And then arrow down to our up to system. You're gonna get information about your computer, your processor, your RAM, but under the Windows specification section, you'll see there's a version number and says 22 H 2. 21 each one something like that The version that's here. 22 H 2 is the minimum required to have access to voice access. If you're on older version of Windows, 11. And you really like this feature. About updating to it. I think they have 23 H 2 out now. The newest one. Okay, so with all that being said. You said this up the first time and it's gonna ask the downloads files. That can run locally. Cause this tool is not required and access to use. This is the benefit of it over dictate. The office suite is that doesn't require internet I hear myself twice this will be fun. So we're gonna play around with some things. What's access wake up? Open Microsoft Word. Like the word. One So as you can see I was able to launch word. Okay. Using my voice. Okay. Switch to edge. Switch to Word. Let's access sleep. Applications, switch between applications. You want to minimize the window, maximize the window, restore the window. So, if you start diving into these types of technologies. Lots of voice, what we call voice commands. How you control this off. So you tell it what to do for you. So the more the deeper you get into this, the more what we call hands free you wanna be where you're not using your keyboard, or commands you learn. Now the nice thing about this technology is you can do what's called a hybrid system. Just because you're using this doesn't mean you can't use the keyboard mouse, especially as you're learning it. You can, yeah, select something and then say, bold that. Hold it. Yeah. Until you get comfortable with doing everything hands free. Maybe you feel like you don't have to go complete. The point is you have that flexibility with voice access. Questions about voice access? Yes. Are there things that are sort of? Looking up against the upper limits of what this can do, or, or is this really enabled to do anything you can do on Windows you can do through voice access. So there there can be some limitations. Especially depending on. Area focus. So let's say you're, you're, you're, you're, you're dealing with a computer programming. You're doing code a lot. Syntax of code is very different than standard English, right? So that's where we hit some barriers. Access Now we have a tool above that. Mr. University, but that's restricted access. Maybe people have heard of a program called Dragon. Really speaking. Okay, if you need to go to that level, you know, there are tools out there. Like that, which are really great because they let you do. So voice give me hands, dictionary, you know, all kinds of stuff. There's needs like that, But. Usually for a lot of. Absolutely work way, we find that a lot of times debate the built in tools do a brilliant job. And these tools like I didn't cover it, but. You can emulate keyboard commands. Voice. So if there's like your word and there's like a special one that I do like control shift and then that's like to put your special accent or does something in word. I can try to replicate that by voice by just saying press. And then the keys. So, but there are some weaknesses like, yeah, you can't do custom voice commands with voice access. Especially like if you want to have applications specific. All the commands that voice access have. What we call global. Meaning the idea is, you should be able to use them very much. Yeah, thanks. Annie, do we have any? Let's check. You can try. No, no, Thomas. The question can you read it? Yeah, so the question is how does Microsoft or dictation do with technical terms in certain fields such as human anatomy? That's a good one. We can, we can see. I've seen it do pretty decent. But depending on how intense that terminology is, it could have issues with it. But I believe you do have the option to add new vocabulary. Voice access. So if you have like a list of terms. The understanding that it would follow English phonetic rules. And it should do a decent job. They may have an example they wanna put in the chat and I'll try it. I also did get this question asked for some of our more biggest schools like what has to do with this vocabulary and I'd be like Right. And, and, and, usually it does a good, some, stuff. It surprises me. Not seeing anything released yet. I'll keep it. Now somebody else, there was a second thing that was posted in the chat. Like composed text could help catch. This is actually good. We could talk about another tool that's built in. You maybe have seen sometimes in word, but they have it in other locations as well. Has anybody heard of Microsoft editor? Okay, so. Did you know it goes beyond? You'll either see it in order if you can actually enable it in a when you're composing in Outlook as well. But in addition to that. Have. Is actually built into edge. If you're writing, say like you're posting something in a discussion board in Canvas. The features that you like to get at least. Least the basic ones in terms of. Misspelled words. And grammar, but it doesn't do the side panel with all the statistics. But you can get the other 2. Right in in edge. And they have that extension. Built in the edge, but they also make it available as an extension fridge, which is weird. They also have the extension for Chrome as well. So if you're Chrome user, you can have editor, and, and use it that way as well. So let me go back. So in. Edge if you go to the. Option here. We wanna go to settings. The phone part is kind of buried. So within settings and edge, if you go down the languages. See they have a writing assistance section. So this is where you would access. Okay. Give me a lot of, a lot of things to try here. Hmm. Okay, let me show this real quick and then I will jump back to the. Take challenge here. So what you want to check is to see if it's on basic or editor. If it's not on editor, then you won't see the options when you're on a web page. Yeah. You fear like Let me personally trying to look at all the settings here. Kind of, me visually it's a mess. It's hard for me to process this. In. Get the extension and it cleans up the settings in a nice little dropdown. So it's a little bit easier to process. But you don't need the extension to use it. Let me go back. Let me go into this discussion boards for a second. Okay. How we can see editor at play in Canvas. So I'm gonna post on this discussions right in Canvas. And. Okay. It's spelled today. Was that chat risk? Oh, you can. I don't move it out of the way. Yeah. So I've done some horrendous misspellings in here. And I also have something that's being flagged. So the Miss Belleys have the red squiggly under them. And the blue double, bars, it negates a grammar issue. I click on these, so just like in Word. And give us those options. If you enable the feature within a editor, you can have it actually show synonyms for each of those words as well. Thank you. And then for the grammar piece, it gives the grammar seductions. So just like you have in word. Now have these options. In your editor. This canvas discussion board that you're doing. You have to manually turn it on for Outlook. There's a, well, it's a option when, so you're in your compose window. There's an option for it. I think it's raining the toolbar. Okay. Editor, you click on it and then the side panel pops up. Alright, thank you. Okay, so. Okay, so I was given this nice long example. We'll try a snippet of it. Go back into work. An atomic dissection of the lateral region of the foot. Inkle showing the morphology. Relationship. The interior. Will be. Annio fibular ligaments. Great. Listening. Okay. So some of it got right, but that obviously that last one was a ton twister and I might have actually pronounced it wrong. I'm not. Medical sciences is not my degree. So. And for some of it, it was getting it right. I think it's 1 of those experiences where you kind of have to kind of trial out and see that. And if it's not, it's not part of the built in vocabulary, add that stuff in. Thanks for trying that out first. Oh no, I never, I never promote, I never insist that this technology is perfect. Even the stuff that's really good that's not the free stuff makes mistakes. So I wanna dispel that right now. Hopefully at least a little bit of a sense of what is potential. Okay. At this point I would be diving into like more the stuff and I think this is good to know about. These are so some of the things we talked about like voice access. You can get through. The accessibility settings that are built into Windows. People know where that is. I want to get to all the different cool things where do magnification or making my cursors bigger. First contrast or the built in screen reader, which is called narrator. People know where to go on there Windows machine to find those. Yes. So you've got 2 ways of doing it. You gotta actually get 3 or 4 ways, but the fastest if you don't like using a keyboard. This key and you. This will bring up built in accessibility. Windows 11 they call it accessibility. You're on Windows 10 or earlier. Called ease of access. They change the name when they make those shift to Windows a lot. But you can see from here we have a whole Options and they're put in the categories. Our first category is vision. Excise, visual effects, mouse pointer, excursors, magnifying. Out of contrasting. Yes. Division sections. If I scroll down here and we've got audio and captions, interactions, we've got speech, keyboard, mouse. This thing called I can go. Just newer that some people don't know about. So there's a lot of these built in. Nice one, then. Does anybody ever feel like their mouse cursor is too small on their computer? Where does? That's what the mouse point Your adjustment is for. Make it bigger. So if you'd like that, can't miss that. And now on the presentation screen, it's actually small still because it's not doing the screen sharing properly. Right now. My mouse cursor would be Start here where this little icon where the mass pointer is and the heights of it goes all the way down here to size. So it's huge on the screen right now. Let's be sure it's not showing it. But we can change colors. Not even doing right now. Interesting. Noise is sharing over Zoom sometimes. But we have these different options for Like, up to accessibility activate it and it bring me back to these options. Yeah, we have a ton of different things we can do in here. What's the eye movement thing? Okay, so the I control is new. This technology has actually been around for a very long time. And what it does is So for some folks trying to use the mouse. Not an issue because they either don't have the mobility or it's painful to do it. For a while they had things called foot mice where you can use your feet. The mouse cursor. I control does retinal tracking. So it follows your eye movements. That will move the mouse cursor on the screen. You don't even have to turn your head because some people Our head mouse is well. Some people they can't do that motion. They can't turn anyway. It's painful to move their head. Well, they just may not have the mobility to need their head. So eye tracking is a way for them to do that. Then use, supplemental technology. So blinks. Clicks. Some of them can be programmed, which I and then. Like a double blame, maybe that's your double click. Like that. Okay, so that's on. It won't because I'll have to actually join. We have equivalent on Mac side as well. So if you're a Mac user and you want to get to the settings. I don't have Zoom set up on my Mac right now, so I can't show this piece. And, but if you're a mac OS user, if you go into Not on the newest Mac OS. The system preferences. You're on the news Mac. This is called system settings. And then from within the side navigation, you're gonna see an option called accessibility. When you go into that, all the options, a lot of these that you see here, you're gonna see replicated on the Mac side as well. As well as some that are not here on the Windows side like live captions. Where it can actually with video audio they're playing on your computer and it'll show captions on your device in real time. Not limited to something doesn't have those encampions. Your machine captions, but you do have that option. Any questions about? OS tools. A lot of things that you can go out here and play with. And help you out. Miss, can you clarify when you just spoke about if you plan a video, does not already have the close action. We all the Do that for you. Yeah, so it's still in beta. Perfect. I think the Mac OS this was the first. News mac OS was the first one when they introduced it. They've had it on iOS for the last 2 versions of iOS. But in keep in mind that when I say those captions, it does machine captions. Of course, accuracy will vary depending on your source content and how you speak. The idea is that it let's say you go out to, you're watching a video, it can be anything. Think you're you have a you're in some app or you're talking with your voice. You turn that on and it's telling you to recognize the microphone. Just in a little box that's floating on your screen, you'll start seeing captions. Generate 7 in real time. Of your camera, is that what you said from your camera app? It can well, whatever your audio source, whatever you're using as a live audio source. It's where it's pulling that from. So, Thank you. I use a lot more on my mobile. Not. You're in some tool that. Oh, fear on. Instagram or TikTok watching a video that has audio. You had that feature running if they didn't have captions and there's audio playing, it would be able to pick that up and then. Options of it. So it's been on a little bit longer in iOS. I think it's a little bit blinded out in iOS. And like I said, it's Bay that. But it's good to know about these things. They're built into your devices. Do we have any other? What's in chat? I'll see you. Good. So. You're gonna if there's no questions that sent from the demos. Oh, here at the end real quick, we're gonna share some resources with folks. Okay. So a lot of the tools that I talked about today. Either ones I could talk at this excellent resource, which will. Right, you researches both. Documentation on how to use these tools. Well as links to video tutorial trainings for these tools as well that works better for you than. So we've just, this is a new resource we developed. It has a lot of these tools and some that we can't talked about. So for people who can see that in zoom. So, The link for this for anybody who can't see what's on the presentation right now. It's HTTPS colon forward slash forward slash. A. E. Board slash BIVB. That will take you to the resources for assisted technology tools that IUKB. Second resource. So we talked about ally earlier. And you would like to explore this in more detail. So we have a in the knowledge base as well. There's an article that walks you through how to use the all formats when you're working with content campus. And that link for that, is HTTPS. All of them forward slash 4 slash. A B dot IU. Flash BHDI. This is a great resource. We've had this one up for a little bit. The gentleman asked me. Earlier but this last one so Questions that Campbell earlier is about. You need a headset microphone when you're using speech recognition or speech to tech software. So we developed this. Okay. Yes. Perfect. Helpful resources about working with these speech to text technologies. And as part of that. That document we have a list of recommended headsets once that we know we have tested that used and then we've had up with. That wasn't me. Okay, look, what? But in that document. Is a list of the headsets. And the link for that one is HTTPS. Forward slash@i.edu 4 slash d. So you have that option as well. And with that, wanna thank everybody for attending today. If you have questions, you can always email them to us. We have our website, which kind of talks about some of our information. And I'm also happy to stick around for a few minutes if you have any other questions. Hey Thomas. Feel free to, you haven't already signed in to sign in the back. There's swag, items back there as well. We have another session in this room today of equity stories at one o'clock so we hope to see you back. Thank you. Thank you

Zoom Recording of Assistive Tech Demonstration

Assistive Technology Demonstration Provided by: Thomas Gregg, Accessibility Analyst for ATAC(Assistive Technology & Accessiblitiy Centers) at IU Bloomington

Beyond Awareness Continued: Equity Stories

Intent: This initiative aims to move beyond mere awareness of disabilities and to nurture equity and inclusivity by learning from the experiences of two exemplary professors, Dr. Kathleen Marrs and Dr. Sharon Miller. Through informational sessions, these faculty members share their stories of engaging with students, including those who are disabled, highlighting the importance of continuous learning and collaboration for all students and themselves. As equity-minded educators with decades of experience, they are committed to fostering an inclusive environment at IU Indianapolis by actively working with AES, ATAC, and all students.

Impact: This initiative encourages a culture of authenticity and innovation within the campus community by showcasing how storytelling can inform and enhance teaching practices. By sharing their experiences, Dr. Marrs and Dr. Miller inspire other faculty members to engage in the ongoing equity, access, and advocacy process. Their efforts promote educational growth for all students and emphasize the collective responsibility of faculty to contribute to an inclusive academic environment, ultimately leading to a richer learning experience for everyone at IU Indianapolis.
View from behind attendees of large screen with recording of faculty member and view of ASL interpreter
view from behind attendees of the speaker standing up mid speech smiling
View of the speaker standing up giving speech with view of ASL interpreter sitting down beside her

Description of the video:

 So I went to the flag of my yard of my yard  number that has a big house, and it seems that I'm not.  But I made it. That's good, only modeled once while I was working only once, coming in. So that's good. That's my chance. So much  so much better. We haven't been able to stop him to pricing.  Okay, we'll get started, so we will  have sufficient enough time for Miller to share in person with us.  So thank you. My name is Mercedes Cannon, and I'm the director of accessible educational services. So welcome and thank you for coming out  today. We're going to continue to go beyond awareness. As we talk about equity stories.  so in this session we will learn about the support of 2 faculty members at Iu Indianapolis and ensuring access.  advocacy and educational growth across campus.  This informational session I'll highlight the storytelling of Dr. Kathleen Morris and Dr. Sharon Miller as they talk about working with Aes and disabled students and students with disabilities.  how they have contributed to the access as  campus community members.  So first of all, I'm gonna read Dr. Mars, bio and Dr. Miller's bio. We're gonna watch Dr. Mars video. She's not. She wasn't able to be with us today. She's at a conference in DC.  And then Dr. Miller will speak to us in person. Take a few questions, and the day will end. So give me a few minutes to tell you about Dr. Mars.  who is a professor of biology at the School of Science at IUPY.  And she teaches introductory biology annually for about 800 science Majors  and honors, introductory biology.  He teaches a project-based microbiology lab for upper level students.  and it's part of an interdisciplinary, Senior Research capstone course  colleagues in biology.  He also team teaches in several interdisciplinary themed learning communities or shares, seminars with colleagues from chemistry, and there are science and biomedical engineering.  Her research has focused on a range of educational initiatives.  Okay, through 12 outreach  undergraduate education  graduate education and teacher preparation  funded through several National Science Foundation programs.  She was selected for the Advocate for equity, accessibility, award from the Iupui diversity, equity, and inclusion.  In October of 2022  for her work to ensure that students and facilities enjoy.  Then we have Dr. Sharon Miller, who is currently an assistant, finds provost for Purdue University in Indianapolis.  providing leadership for Purdue and Indianapolis that focus on correctional and the student experience.  Dr. Miller received a Bachelors of Science Degree in Material Science and engineering from Purdue University, West, Lafayette, Indiana.  and a Master's of Science, and Ph. D. Degrees in Biomedical engineering, the University of Michigan.  Ann. Arbor.  Most recently she served the Iupui, BME. Department as associate chair  Director of the undergraduate program  have been developed  implement and assess curricular changes and embedded engineering design.  ethics and technical communication  in the Biomedical curriculum  her grant funded engineering education work has been supported by the National Science Foundation.  the National Institute of Health  and the Office of Naval research.  In addition to many internal seed awards.  this scholarship of teaching and learning and engineering education focuses on learning, undergraduate student self advocacy relates to design achievement.  Dr. Miller enjoys teaching, advising, and mentoring students.  and has been awarded the outstanding materials. Engineer  2024, Iupui advocate for accessibility and equity. Award 2023, and the Iepu, I trustees teaching award 2022.  The IUPU. I. Wisner  boats  Outstanding Faculty. Award 2021, and the Jaguar Academic Advising Association, Faculty Advisor of the year 2020,  and the Aurora University mark and markets. Trumbo excellence in teaching award 2015  effective coaching  senior Capstone design teams have led to local and national design student awards, such as the NIH.  Then they chore with all the bulk.  and IH. Vedore well. The view award in her creative leadership has forged opportunities for students to connect  several Indianapolis. Companies and resources, including the Iu School of Medicine and the Iu health 3D innovation lab.  Thank you.  Alright. So we're gonna start with Dr. Martin, and then we'll hear from John.  Good afternoon, everyone. I'm delighted to be here today to share my experience as a faculty member. My name is Kathy Mars. I'm a professor in biology, and I teach a large enrollment biology, class biology. K. 101. I learn more every semester about fostering an accessible and inclusive classroom, thanks to the work of Aes and our students. While I can't be here in person, I'd like to take a few minutes to share about my engagement with students in my biology class.  So over part one over the course of my time on campus. It's been my privilege to have taught over 15,000 students. I've worked with a diverse range of students in lecture hall classrooms. But here I'd like to focus on the biology labs a space requiring the most creativity in ensuring accessibility.  So biology labs usually require active participation, using microscopes to see images following detailed protocols and procedures where each step is important, often transferring liquids or other materials into test tubes and looking for color changes that are usually an indication of a positive reaction, and then also doing this under appropriate lab safety considerations. So this presents a number of  considerations to make sure that the labs are accessible to all, one is making sure that the bench space is configured  in a lab like this. The lab. The the bench is where the work takes place. So while our current K 101 lab is far more accessible than most  in multiple semesters. We've made sure to configure the lab tables to enhance accessibility for individual students ensuring a greater ability to participate. We've also introduced tactile materials for blind students lab work can really pose a challenge for blind and visually impaired students working with Aes and one of our blind students, we were able to incorporate multiple tactile materials into lab to facilitate learning again, broadening how students could engage fully with lab activities.  And then often in semesters, we've had interpreters. So students who are deaf or hearing impaired can fully participate in lab discussions.  understand instructions, and interact with their peers and instructors and instructors by working through interpreters. So this again ensures. All students have access to the same information and success in lab processes.  Now, a second example I'll mention is more specific. And this is a student I worked with as as a student and then as an undergraduate. Ta. So this student is a disabled student who uses a wheelchair now we, when she was a student in class, we made sure to configure the lab bench to make sure that she could excel in the lab which she did, and but beyond that I learned a lot from working with her.  So she approached me about doing an honors project on disability justice. She let me know very directly that some of the links I had highlighted in K. 101 course material were out of date.  Through her project we discussed crucial topics, such as identity, first versus person, first language. I was familiar with person first language, but I had not realized how important identity first language was for many people. Our discussions and work on her honors project not only enriched my understanding of disability, justice.  but by incorporating her project into the K. 101 curriculum as a canvas module has also enriched the knowledge and awareness for students and teaching assistance, creating a ripple effect of increased awareness and understanding. And then, finally, this student returned to K. 101. This past fall semester to become an undergraduate ta, assisting the weekly lab and helping a future generation of students succeed in the class.  Alright, I'd like to now take a moment to just say how, when advocacy became a real catalyst for positive change. A little over a year ago I was awarded from the Diversity, Equity, and Inclusion Division, the advocate for Equity award, and this was a real honor in my career, and it came from identifying a gap  while serving for a year in the Iepui Honors College. I realized that the the large glass entry door lacked a push button opening to to allow that door to open for all. So we worked to install a push button accessible door, so that all students, regardless of physical abilities, could access the honors. College space seamlessly, and students and visitors had equal access.  And I'll conclude by a part 3 is mobilizing for change, and I just like to mention a few things about the future. Now we know there's still work to be done to ensure that accessible design is integrated into science and engineering lab construction and across university classes.  So I feel that by sharing our experiences as we are today with faculty staff and students, we are fostering an environment where we work together to implement accessible practices across departments, across schools and raise awareness to empower the community to make informed decisions that positively impact everyone.  I see 3 trends on the horizon. One is increased awareness and advocacy. So more campus architects, faculty members. Administrators and students recognize the importance of inclusive design and are actively advocating for its implementation.  Technological advances, assistive technologies, online learning platforms like canvas with built-in accessibility, features all break down barriers and create a more inclusive classroom. And then, finally, policy and regulation change. There's been a notable shift towards stronger policies and regulations that promote accessibility and education.  I have long felt that our campus has been proactive in dedication to comply with and exceed accessibility standards driving forward the implementation of accessible design.  In closing, I want to express my heartfelt appreciation for the incredible work being done by Aes from the director and staff to the students involved. Your dedication and commitment to fostering accessibility and inclusion on campus are commendable, together with the support of our campus community, we will continue to mobilize for change and create a more inclusive future for all. Thank you.  Awesome. I wish she was here. We could ask questions, but we're gonna just transition right into  driller, who is very familiar  with Dr. Mars, and  excellent. Well, welcome, everyone. Thank you for taking the time today to come here and myself.  Here are some of our experiences. What's really neat is, Dr. Mars gets to teach biomedical engineering is, in addition to other students on campus and my background and biomedical engineering overlaps with her. So I often hear all the great work that Dr. Mars does when the students come into our program, and they also speak volumes of how she not only is aware of promoting accessibility for all, but  in in the classroom, like she just explained in the Biology lab, but also experiences so many, many students have crossed. You know my path, have in the chairs in my office and shared how Dr. Mars has gotten them to research with a specific research faculty member as well. So  I'm honored to share the stage with her today and share a little bit about my journey and  additionally express my thanks to Aes for for this honor  apui in general. So I know. Mercedes gave me a a nice sort of template to sort of think through as I. I approached this and and join you today. And so I just kind of wanted to start from the top.  Dr. Mars jumped right into biology lab. And I'm gonna start a little bit more broad and just share my experiences to date as an educator. And some of the things that I learned were  having students with disabilities in my class sort of cross my path.  So I I've been in higher Ed as an educator for over 15 years.  and one of the the neat things that I think I bring to the classroom is that I have taught at a community college.  small private Liberal Arts College, outside Chicago.  Iepu, I. And now transitioning to Purdue, which is, you know.  even larger schools. So I really have experiences through large institutions, but going through  as an educator in the classroom, seeing all the different types of places that our students either  start and finish their their pursuits academically, or transition from community, college to Ibui, or the like. So all these bases I have to say barn on the iepui has given me the most resource for my  inviting different ways and perspectives to helping all students, not just students, with disabilities that cross our classroom classroom. So I'm thankful. I Api. For that  my discipline, my training, is in biomedical engineering, and and Dr. Canon also mentioned, my undergraduate was in material science engineering. So I I definitely got involved in that, because I was really intrigued on how, how things actually break, which is, you know, not necessarily something here every day. So I was in definitely in the discipline of learning how how stuff breaks, and I still am fascinated with that. But after  my education at Purdue I really wanted to learn how things, how, how we can repair the body so like taking my knowledge from how things break, and then how we can fix the body. And so I did a lot of my masters and Phd. And even my post doctoral work was was in areas where I was investigating materials that definitely help.  How do you regrow things in ways that so that we can again? So it's, it's really an interesting parallel, because I've used a lot of those skills in the classroom. And now I definitely engage in hearing education in a way to further my academic pursuits. In addition to learning how our students learn in the classroom.  And so when I came to I Apu, I started in the Biomedical Engineering Department. I'm still in the Biomedical engineering department, and I I have the pleasure and the privilege of of teaching really, fabulous students, many of which come to our classrooms meeting adaptive education services. Some do not, and some do. And so it's been really eye opening to learn from the student that might need extended test time. Taking  to the student that might need a notetaker in class, and I was glad to hear in Dr. Mars this presentation she was mentioning, you know. Maybe  filter accessibility in her lab, etc. So there are a myriad of reasons why a student might come into our classrooms needing assistance for  ensuring that they have access to all of the material within the class, so that everyone can learn.  And and we also have in a Bme department visually impaired blind student. And so that was really where my journey began within the Bme department, and personally, you know.  creating these eye, opening moments, not just for myself, but for my peers and colleagues around.  I wanted to, you know, hang there for a little bit longer. So you know, definitely like I mentioned over the years, had a a variety of students with different needs, but specifically you know the visually impaired student that we have in our program now gave me the opportunity  to connect with a couple of folks. And so.  first first of all.  as an advisor.  talking with a student and understanding their needs was was probably one of the most impactful conversations at the beginning, learning.  you know what the student needed within the program  but then, navigating the educational support systems that Iepui has, so that we can  accessibility for not just the student, but all blind or visually impaired students within a difficult engineering  curriculum.  Biology lab presents. It's Dr. Mars talked about microscopes and seeing images, etc, even for some folks that were in her classrooms and in in engineering. We do use microscopes in Vme. We also have a lot of software.  And we're we're definitely a math, heavy field, as you're probably well aware. And so you know, in initial conversations with with that, our students, understanding how equations become accessible, for all was really eye opening. And so, you know, first talking with the student, then recognizing there was, there's an entity on campus that provides support.  Students in general that that have accessibility needs  the next sort of layer that sort of expanded. My vantage point was working with  peers. My faculty peers within the department.  And so it was clear from the beginning that there was not necessarily one piece to this sort of puzzle to help the student have the resources and the ability to learn the material in a way that was congruent with everyone else. In the classroom  there were many different facets to shuring  this student in particular all the things that they needed in order to be successful.  One by one, talking with folks within the department, understanding  myself how to plan forward how to think even semesters ahead, so that there were other additional entities on campus that could provide the student the resources they needed, and then translating that to my peers, when student went to engage within their classes, was, It's been a journey, and it's so ongoing like this is something that doesn't just end with one student. It's  has really expanded. The conversation within our department. So I'm I'm thankful because not only was it finding accessible software so that we could  communicate in differential equation.  It's understanding how we can ensure that learning outcomes are really the the fundamental of what the curricula is designed to provide a student with the skill.  and that there's not only one way where we assess  those learning outcomes can be, because there can be multiple ways that we achieve  together. So these these pieces have really, you know.  bolstered and reinforced a lot of my curricula experiences and sort of  pieces that I have thrive to integrate within not only biomedical engineering, but stem engineering broadly, but  making that a piece that's contagious to others as well. And I come from a discipline that's very assessment. Heavy  extremely, you know, viewed from an accreditor's standpoint.  Ensure that you're meeting learning outcomes for all students with programs.  So it has been  really,  thankful for the experience, not only for myself and all of the materials that I was able to revamp for this one particular student, now  more accessible for all my students.  So in that way, it's really sharing that experience with my peers so that they can begin to see how they can adjust or implement. And even if they don't necessarily have a student in this particular case that has is blind, they don't have a blind student in their classroom, aging in that broader conversation, so that we can  forward together. And so, you know, in sort of closing, and I'm happy to answer any questions. You  can't speak for Dr. Mars, but I like, I said. I know her lab pretty well, and in the way that our students engage with it. But for the Vme curricula, or any questions you might have. But I really do think, you know, and I'm thankful for the honor.  When I learned about it, I actually had to go for a walk because I thought I was. This is something that everyone should be doing in their job something we should be talking about all the time, how we can make curricula better for everyone. Not necessarily. When we're faced with  particularly, you know a challenging representation of how I can communicate these learning outcomes or this knowledge to a specific individual  so thankful for the opportunity to continue that that dialogue with everyone, really zoom, and and that's supported through Iepui and beyond.  like I mentioned, I worked at a couple of different universities, and I feel like this is this is a human pursuit. This is not an Iui or a pursuit. This is a collaborative effort that together, when we put our heads together, and we figure one thing out to to better the learning outcomes of one student. It's definitely  super excited as how we can continue that. And I'm very proud. I walk around sometimes, and I see some of our, whether it's a visually paired student or student in a wheelchair like Dr. Mars mentioned. If Ui or Indianapolis in general really does  augment the the experience. And I've been very proud to be part of this ecosystem in Indianapolis that can really bolster the options for those that might need adaptive educational pieces when they're at least within the academic confines of trying to achieve together. So so thank you, Mercedes, for this opportunity. Thank you for all the room that we're able to to come today and, like I mentioned, I'd be happy  questions if you have.  This is Dr. Miller.  and I have any questions.  Nielsen.  I'll make  so first of all, I wanna thank you, Dr. Miller. And even in Dr. Mars's absence, Dr. Mars, for your your stories about how you have supported students with disabilities. And just, you know the importance of being thought partners with aes, and the students to create that experience. And I was just really glad to kind of you say that this is.  you know, kind of part of the human experience, and this is something that every faculty member should be naturally, because that's not the experience.  you know, most senior universities of all faculty members. I think, like, sometimes there is a  there can be a disconnect around. You know what inclusive classes look like when we're thinking about accessibility. And a lot of that, I think.  stems from kind of a lack of  knowledge around what accessibility inclusion looks like. Because we haven't always talked about it in the same way that we talked about  inclusive practices, you know. In other aspects of faculty classroom preparation. And so I think it's important, because sometimes it can be add on, or additional, you know, responsibility or burden, rather than you know a part of being. And so how can we  elevate. So I guess now this is the question part. So how can we elevate this  philosophy  to faculty in all areas so that it becomes more of a a philosophy and a practice rather than you know, kind of like disjointed like some faculty, are more known to be you know, inclusive in this way versus others have to kind of learn like, how can we make this  philosophy for faculty?  Silly question? Thank you for the  for the question, really, and I don't know if I have a specific answer  that.  however, I do know. It takes  individual efforts to take selective effort. I think Dr. Mars, at the end of her presentation also mentioned  continuing to support policy efforts that  shape this as a community. So that's as a whole. So whether that's  policy making institutional levels. So continuing to advocate  there. But I recognize as an individual who also, I  big proponent for co-teaching or peer teaching, so that  you can learn from one another.  So I've had multiple instances since having the student  I do sit in on other  multi lectures and notice, you know, the the small things that each of us does as we present material, and whether that's not reading an equation.  whoever who's  just pointing to a slide, saying, I'll give you a minute to read this  and so, but then, not just noticing it, but then engaging in that conversation here to ensure that  there is recognition day by day in our sort of daily experience that you know when you are  excellent, that we were talking about this, I think we may have excluded a student when got to this point in the lecture because of Xyz and then revisiting, how can we? How can we make sure for the remainder of this semester that we're ensuring  very specific answer to your question. But I think it's maybe demonstrate some of those  smaller moments that we all internalize and continue to advocate that together, and we're happy to work together and call one another out if we're in this place where not making our our lectures and and please help you, I'm sticking to education, this realm  accessible for for everyone.  So there's there are large things. And then there are very small things. And I can. That's just one example that  Ed  be responsive? Can I just add optimum question. And then  so is there a way? As we think about Ctl, the center for teaching and learning  that we can  expand our reach or partner with steel. Like to.  I'm sure they already have some curriculum on, but even more like to, you know, to grade kind of some of these practices.  CTO is a great way of helping Ryan  absolutely. And and I think one of the the  best tools that I now employ routinely on canvas is accessibility checker.  It's just it's almost like my alarm clock to remind myself, what else can I be doing? And so to that question.  engaging the Ctl. In  maybe  exploring, visiting different departments on campus to ensure not just the accessibility checker on campus is being used. But  departments understand the different support systems that this Vto. And also provide as instructors for classes. And it's never a one time piece. You know, it's it's often a recurring.  And and as a faculty member that sat on different committees throughout my career to date  our undergraduate curriculum  meetings within each department mostly that are sort of the target for that definitely have a champion within each each department. I think some of that can spread.  Arlington.  It's  me.  Do you know, if much is going on in K. 12,  help students  and disabilities we're addressing. Yeah, I'm less informed in the K. 12 space. So I don't want to speak.  All I, the only anecdotes I have are those  good share and save them in my  I'm my name is Jonathan Stefan. I'm with aes you mentioned?  I think the word you use was cultivate  What was the word that you used  perfect.  and I Scott  allies, I think maybe something like a  how. How can we?  You have any  words of wisdom or suggestions for us  at Aes to to cultivate these kinds of  advocate Allies champions, maybe champion stuff. Yes, we got there.  So how do we sort around your observation and your experience? Are there suggestions you have for us to cultivate those  champions.  Yeah. And I like, I can. Only, you know, I guess I give my  perspective as someone that has that on an undergraduate  curriculum committee. There are graduate curriculum committees as well.  Department chairs, right? So the folks that are closest to the current.  Sometimes I feel, understand the the limitations and  advantageous pieces of curricula, and also, at least for my discipline.  Sort of accreditation. Assessment means so they really see, sort of from their vantage point all the pieces within the department in order to  liver quality, to their students. And there could be multiple programs. So I think, thinking creatively on engaging folks at that level would really, you know, resonate with them, so that if there are pieces that whether it's Aes or the Ctl. Or Atac, or other entities on campus can  plug into more. So  would really be at that level. Others are advisors. But our advisors, you know, they're they're definitely  good sources. So like maybe listening sessions with advisors to hear the stories, because they can have those one on one personal conversations with students which I don't think I would sort of be up here talking with you if I wasn't an advisor.  cause. I don't know if I would have had the time with the student one on one to understand  where I needed to meet  at that moment. So I don't think it. While it might not be in the job responsibility of the advisor to find the technology, or but I do think there's rich information that they gain that others within the department don't necessarily have  the access to you because they build a different type of relationship with the students.  Dr. Miller, I appreciate  being here and and being as transparent as you are about your own experiences and how you've navigated your decisions. You've made to work across community college to the larger the larger spaces, and also how you appreciate the humanity of people.  What situates with me is how you say you walk around and take it in.  you know. Take in what you see and what you what you're experiencing, what you understand about curriculum, what you understand about your own discipline.  and then those you work with within  a larger context, such as University and as the director of Aes, and the reasons why my  my desire is to hear storytelling right this, this, this actual piece of it right is that we will never know how you got there. If we didn't invite you to tell us right.  and then inviting you to tell us that I think about the years of work with you and the student you're actually speaking about, and also just the staff, you know, as a chair, right as an advisor as a chair. You're speaking out of different types of levels of higher education where decisions are made and things are impacted towards students.  So as we think about folks who write curriculum, think about different folks, we can possibly invite to the table as we continue to move towards more of an external office, right? Interacting with the very people we interact with on a regular basis without each other, knowing that as we continue to do that, and as we continue to think about what other programs it and brown baggings, we could have.  what what would you suggest when you think about the years you spent as the chair, working with your colleagues.  as an advisor and as a chair of biomedical engineering.  What did you discover as you were discovering things about the students.  What did you discover from working with your colleagues? That would be important for us to be thinking about as we're thinking about brown bed luncheons. Continual conversation around the community of practice.  I know it's a lot. I think you got. No. And there there are a couple of thank you for that question.  Summary, because there's so many different facets. And it's been it's been a journey. So, and I'm trying to condense it into a short period of time, one of the sort of  surprising pieces to me. I don't know why I was surprised at the time.  but the interest  of peer students  to engage their peers and helping them.  And the reason I bring that up and sort of zone in on that which could be a brown bag lunch by inviting students that have worked with other students in this situation as note takers, or  you both  aids auxiliary aids  so that they can share what their experiences have been, because I learned just as much from this the aids as I did the student during situations.  and some of these pieces really  just amplifies the respect in the room, everyone.  and it creates a an environment that you want to be a part of, because every student within  within the lab or and we've had many labs, you know, speaking of biology labs, we had electronic slabs, wet labs, organic slabs where we did break more things. You know all these labs that the student definitely engaged with. But students always stepped up  different ways, whether they were an aid or not. So I feel like that would be  one area that maybe  hasn't been explored enough to really learn from from the peer students. And they're the  better sources than students, right? They're they're the ones to to educate us for sure.  I think the others is just, you know.  maybe advisors, maybe department chairs.  starting with some leadership within the different colleges.  So learning and I think what I learned, and it took me a little bit was learning the cadence of understanding how I needed to sort of get my ducks in a row to ensure I was effective as an instructor.  and that was a heavy lift was not easy, and I had to make a lot of videos and in it  in  make sure that I was okay with my pacing in my videos, so that I  I had to say every thing that was on the slide, every equation  so understanding and level setting  my classroom was also something that I worked hard at.  So understanding the timeline and the timeframe, and that there does exist support if it's  if and we're talking very specifically about one  student situation. But I think this  it could be expanded more broadly for different  adaptive services that might be in.  Let's say, students.  nobody else  you wanna on Zoom has a question feel free to type it in. We're entering the chat.  not keep anyone any longer than they need to be  here. So if there's no other questions  in the chat or in person. Thank you so much for the opportunity.  Thanks for being a captive audience. It's in. Live.  appreciate everything with everyone.  We're an app  I've been to met some of my great colleagues at veteran for for students.  Yeah. So if you want to  everyone on zoom, there'll be a survey link coming your way. So please take the time to fill that out, so we can here  absolutely  later.  Also.

Zoom Recording of Equity Stories Event

Presented by: Dr. Kathy Marrs, Professor of Biology in the School of Science at IU Indianapolis and Dr. Sharon Miller, Assistant Vice Provost of Purdue University in Indianapolis
Photo credit: Thank you Jonathan Steffen (Testing Lab Coordinator) for capturing beautiful photos from these events!

Disability Awareness Month Evaluation

AES asked the participants and attendees to complete an anonymous online evaluation after each event, so we could gather the appropriate data. In the interest of transparency, we are pleased to make those results available for anyone to view. 

Link coming soon

Many thanks to Sonia Ninon, Director of Research, Planning, and DEI Evaluation for developing the evaluation, gathering the data, and writing up this very detailed report of the results. Thank you so much Sonia!