Newfound Awareness

I found the discussion with Erin Sember-Chase from Cornell’s Student Disabilities Service to be eye opening. I had no idea that so many students on Cornell’s campus are affected by disability. It made me more aware of how I perceive disability: as something visually obvious. However, there are so many mental or cognitive obstacles that seemingly physically-able people have to overcome on a daily basis. I haven’t grown up aware enough of disabilities and it is not addressed enough in my communities. Because of limited exposure, I have had an unrealistic image of a disabled person. I enjoyed hearing people’s personal anecdotes surrounding disability stigmas.

I do feel conflicted about the word “disability.” It implies that someone is a less able person due to something they’re affected by. And I don’t think that’s a good way to construe a setback. I think it impedes on growth-mindset.

Disability at Cornell

This past cafe’s discussion about disabilities spoke about both visible and invisible disabilities here on campus. I personally found our discussion of extra exam time and other academic accommodations very relevant and interesting. In such a competitive academic environment people often view disability accommodations as an awarded advantage. We spoke about the reality that students with disabilities that effect their learning are simply compensating for the obstacles they face in order to create a “level playing field” so to speak. On the other hand, students who receive these accommodations often feel it is sign of weakness to have a disability or that their situation is illuminated by alternate testing situations and curious peers. Ultimately the solution to this ignorance to the reality of academic disability accommodations is solved by educating not only people who have disabilities but entire institutions in order to remedy the social stigma surrounding them.

 

The Unspoken and the Unheard of: Disabilities at Cornell

Last week, I attended a Rose Cafe where Erin Sember-Chase from Cornell’s disability service came to talk with us about the prevalence of disability at Cornell. The most surprising fact that I learned from this talk was that the ADA (American Disabilities Act) was only implemented in 1990. That, to me, seemed far too late. However, what was most interesting to me about this talk was the discussion of disabilities at Cornell, particularly those that cannot be physically seen such as academic disabilities. The first that comes to mind is when professors mention that students who need extra time for examinations can be accommodated. Although it is excellent that these kinds of accommodations are provided for people who need it, it is also problematic, in a social sense. There is already a stigma present around disabilities, and when you are singled out for your disability by the means of which you obtain your accommodations, the issue becomes quite contentious. A perfect example of this is when you obtain separate testing accommodations, but then on test day your friends wonder where you were and then you have to explain why you were somewhere else. Some people may feel completely comfortable with this, but others may not. The most important thing that this reveals is that although disabilities are increasingly become more and more normalized, in the sense that people are aware of the vast kinds of disabilities present and the numerous accommodations that can be made for them, they are still something that can cause social distress. Keeping this in mind, it should be our goal to destigamatize disabilities by talking about them more in a positive manner in order to better educate all of society on how to create an environment where people with all kinds of disabilities feel comfortable and welcome, no matter the severity of the disability or whether they even have a disability.

Disability Awareness on Campus

This Rose Cafe was an engaging talk where lots of the students who came could deeply relate to the topic of disability. During the talk, we discussed an interesting concept about students who receive extra time during exams. Often, people look at these students and believe they are receiving an unfair advantage; however, that is not the case. Extra time simply allows people with disabilities to bridge the gap between them and students without disabilities, thus, this extra time makes students equal in a sense.

I could personally relate to this talk because my older sister Mona has down syndrome. Often, when I tell people this, their first reaction is a sympathetic look accompanied with an “awh” as if her disability is a negative barrier that prevents her being “normal.” Only people who get to know Mona realize quickly that her personable character, kind being, and smart thinking, make her a person anyone could easily relate to. Part of the movement to destigmatize disabilities is to realize the fact that disabilities are just physical or mental constraints or barriers that do not define an individual.

I am a transfer student from UC Berkeley which is the first school to accept a person with a disability. The institution is rooted in making the school accessible for all. One tactic they used which could easily be carried over to Cornell is a video about accessibility and extended time. They played this video during freshman orientation for all the new students to see. Short, informative, and catchy, the video was a perfect tool to educating the students.

Disability Inclusion at Cornell

The Disability at Cornell chat with Erin M. Sember-Chase really opened my eyes to the battles that people diagnosed with disabilities must face. Erin herself shared a personal story that reflected the absence of a disability center at her college while she was an undergraduate student. At Cornell today students with disabilities are not rare, even though it may not be immediately noticeable. Erin talked about breaking the stigma associated with disabilities. Although Cornell works to help ease students academic life, it is up to the students to connect with any disabled students socially. Today, 1 in 5 Americans have a disability. It is very likely that you know someone with a disability, or at least know of someone with a disability. We have come a long way since 1990 when the ADA was first passed and I believe that we will continue to grow in years to come. Hearing the personal experiences with loved ones with disabilities really shows how this is a topic that is close to everyone’s heart. I believe that a disability center is an amazing addition to schools that helps make everyone feel included regardless of any situation. The advancements that have been made in the history of the university is inspiring. Erin herself has pushed and helped to make these advancements possible. I hope to someday make a difference as significance as this.

Deconstructing Disabilities

Last week at the Rose Cafe, I learned about disability history and disability at Cornell with Erin Sember-Chase. I learned that the ADA which prohibited discrimination based on disability was only instituted in 1990, a mere 27 years ago. But unlike other marginalized groups, the fight for rights for people with disabilities  has never been as visible as other social movements, such as the civil rights movement. At Cornell, most professors will at least briefly mention special exam accommodations for students with disabilities but that is usually the extent of the discussion of disabilities. In our society in general, there are a few public accommodations of disabilities, such as handicapped bathroom stalls and parking spaces. Before our talk, I had honestly forgotten about these sort of accommodations for disabled people. In a way, that is a good thing because it has become so normalized to me but these adjustments are often not discussed. Additionally, while useful for physical disabilities, these accommodations do nothing for other disabilities that are often less apparent. These “invisible” disabilities are unfortunately just as pressing as physical ones.

We discussed the large social stigma that is associated with disabilities and the way that people with disabilities themselves are taught to overcome their disabilities rather than embrace them. We talked about how disabilities shouldn’t need to be justified or explained but rather celebrated and understood. I am grateful that I was able to attend this cafe because it made me think about disabilities and the amount of people who face disabilities much more than I ever do. As a society, we need to talk about disabilities more widely so that its stigma can be lessened and people with disabilities can feel more comfortable and accepted in their lives.

Disabilities Discussion

This week’s Rose Café with Erin M. Sember-Chase was incredibly interesting. We discussed the stigma of disabilities and the consistent battles that one must face while dealing with disabilities. I loved how everyone shared their personal experiences with close loved ones and disabilities- it shows how we can all truly understand and relate to each other despite the fact we may not have a disability ourselves. I shared how one of my best friends had extended time in high school due to her dyslexia and slight attention deficit and the stigma she often faced. Despite being in APs and honors classes, everyone always seemed to think it was strange she was allotted extra time – when I know for a fact that it was the quite opposite of strange. It was interesting how we discussed how extended time is assigned too, for I did not know much about it. It was also amazing to hear how she faced incredible difficulties even at college – especially the rude professor who refused to use a mic despite her difficulties. I commend Erin Sember-Chase in her strength to have dealt with such adversities with pompous, inconsiderate professors!

The Division of the Disabled and Non-Disabled: How Our High Schools are Failing at Integration

Last Wednesday, I attended a talk given by Erin M. Sember-Chase, the Assistant Director of Cornell’s Student Disability Services. During this café, we discussed the daily struggles of handicapped people; students also shared their own personal experiences with disability. This chat brought to mind memories of my high school’s treatment of disabled students.

In my high school, students with serious mental/physical handicaps were separated from non-disabled students both by classroom and floor. For class, the disabled students were relegated to the basement, a place to which no one else really ventured. It set up a weirdly segregated environment in which there was this fraction of the school that I essentially never saw. Because I go to a small high school, it was strange and sad at graduation when I did not recognize a few names called to the podium for a diploma. All of these unrecognizable names were the names of disabled students.

Obviously, there needs to be a better system of integration between those with and without disabilities. We need to be exposed to what the real world is like, rather than kept in bubbles not representative of the global population. Integration of non-disabled and disabled students must be carefully and smoothly done, though, as I learned from another student at the café. Her high school used a “shared classroom” system, which put disabled and non-disabled students into the same classroom. The student said that the atmosphere of these classrooms was unsettling and uncomfortable, as teachers created an environment in which they made clear that the disabled students were slower than the non-disabled students, vocally encouraging the non-disabled to help the disabled with the material. This is a lose-lose situation for both sides: Disabled students were made to feel inferior, leading to diminished confidence, feelings of competence, and self-esteem; meanwhile, students who weren’t disabled may have felt they were spending valuable class time helping other students instead of getting the educational support and instruction that they themselves needed. Additionally, they probably felt uncomfortable in these positions of teacher-asserted authority. There needs to be a better system where we can have integration with equality, where everyone gets to feel confident and competent and gets to focus on their own learning.

Disability Inclusion at Cornell

Disability at Cornell…to begin, most people don’t realize that disability even exists at Cornell. Many assume that if you don’t see it, then it’s not there. A lack of disability awareness is a problem that extends beyond our campus community–many people in our society don’t even know about the disability rights movement in our recent history.

This Rose Cafe was an excellent opportunity to start a conversation about an issue that’s not discussed enough. It was also interesting to hear Erin’s personal experience about being a college student at a time when there wasn’t such a thing as a campus disability services office, and it helped me realize how times have changed since the ADA was passed. Furthermore, this event was a great opportunity to start a conversation about how we can be more inclusive of students with disabilities on this campus.

A Discussion about Students with Disabilities

Last week I went to a Rose Cafe where we talked about disability services at Cornell. I was really surprised to hear that the ADA wasn’t passed until 1990 because it seems like such an important piece of legislation, and I thought that it was passed much earlier. Another thing that we talked about was how during elementary/middle/high school, students with disabilities had their own classrooms and we never really got to interact with them. I remember in high school that students with disabilities even ate lunch at a different time/in a different room! Even though we went to the same high school for 4 years, we never really got to interact much with students with disabilities. I think this needs to be changed. I realize that some students with disabilities may need a specific learning environment to learn best, but I think that everyone would benefit if we all got the opportunity to talk to one another. Even something simple as having the same lunch period would facilitate that. I think that everyone has a unique viewpoint to offer, and that we would all learn something if we all got to share our viewpoints with each other.

 

Destigmatizing “Disability”

Last Wednesday, I attended the Rose Cafe where Erin Sember-Chase discussed disabilities in general as well as how the Student Disabilities Services office works with students with disabilities. I was surprised to hear that one-fifth of all Americans have a disability and that the Americans with Disabilities Act was only passed recently, in 1990.

I really enjoyed hearing Sember-Chase’s experience of going to college with her hearing impediment just after the ADA was passed. She explained how there was no student disabilities office at that time, and had to fight for her theater professor to wear a microphone in a 100 person lecture hall. In addition, her use of a hearing service dog was met with criticism at countless restaurants and shops initially.

Sember-Chase also explained how students with non-visible disabilities (the majority of student disabilities registered with SDS) receive testing accommodations for extended time or separate rooms among others. We discussed how many people view these accommodations as giving the students an advantage over others, while in reality, it levels the playing field. For example, a student who needs twice as long to read an essay prompt should receive additional time to do so.

We also talked about the various stigmas of disabilities. Professors try to reduce the stigma academically with syllabi that openly invite students to email the professor if they need accommodations. Sember-Chase raised the question of how students can reduce these stigmas, and I think we can accomplish this with more conversations like this Rose Cafe, so that those with disabilities are not discriminated against and are not defined by their disability.

A Need For Awareness

This past Wednesday, I attended the Rose Cafe on disability at Cornell. After hearing everyone talk, I feel strongly that we need to better educate others, starting from an early age, about people with disabilities, and the struggles that they go through in our society. Several people at the cafe mentioned how, at their elementary, middle, and high schools, many of the students with disabilities were kept in a separate “special education” classroom. My school district did the exact same thing. As young children, we may occasionally run into these students in the halls, but we are effectively taught that, if they cannot be in the same classes as us, then they cannot possibly be anything like us, and thus they cannot be complete members of our society. Honestly–and quite tragically–I think that last Wednesday’s Cafe might have been one of the first times where I had the opportunity to knowingly meet with people with disabilities as people like myself, not as the “special education kids.” I truly found the experience to be enlightening, and I truly wish that I had been exposed to such an opportunity earlier. By giving young students the chance to meet with those of their peers with disabilities as equals, they have the opportunity to realize that people with disabilities are not so different from them.

Furthermore, we should be teaching students about people with disabilities, just as we teach them about other marginalized groups. I was taught plenty of information about the Civil Rights movement, and the women’s rights movement, and the news is constantly covering the continued efforts of these and the LGBT+ rights movement to this day. However, I have never learned about the disability rights movement–in fact I did not even know there had been such a movement until the Rose Cafe. By teaching students about the problems that people with disabilities face, perhaps we as a society will finally recognize the need for change. That change cannot happen if nobody knows that it is needed.

Re-Invisioning the Invisible: A Conversation about Disability at Cornell

I really appreciated that at this Rose Café, the Rose community could come together and have a conservation about the experiences of people with disabilities—a subject that is often avoided or overlooked. I totally agreed with several students’ point that living with a disability becomes invisible because, often, explaining that you have a disability is met with stigmatizations or uninformed assumptions rather than understanding and conversation. These points made me consider that perhaps this stigmatization of disability is a symptom of broader American social norms that tend to find blame for a variety of circumstances—whether that be financial hardship, difficulty finishing a test during a given class period, or bouts of depression—and place it on the individual. Thus, rather than viewing that fact that some students get extended time to finish their tests as something that ensures that this student has an equal opportunity to succeed, people may falsely perceive this accommodation as signaling that this student has less competence or receives unfair treatment. I think that when an individual speaks out about having a disability, others, not recognizing what is contributing to these assumptions, may either falsely assume that this individual is not working hard enough to overcome their disability or start to view this individual as lesser. American society often seems to have sort of a pervasive inability to accept difference, and this inability to recognize that every single person has different hardships, experiences, aspects of self leads to a system of categorization that falsely stigmatizes some aspects of self or hardships as “abnormal.” This stigmatizing label, then, may contribute to this feeling that a disability is something that should be hidden, preventing conversations that could remove the stigma from taking place. Accordingly, I think that having conversations about disability like the one we had tonight and sort of creating awareness about the experiences of individuals with disabilities at Cornell and beyond during orientations or other events, as one student mentioned, could be a way of making it easier to have these conversations that deconstruct the stigma that fuels distance and allows false assumptions to persist.