Disability Reflection Paper

In Nancy Mairs’ article for The New York Times, “Disability”, published in 1987, she expresses her distaste with the media's representation of handicapped people. Mairs, who struggled with multiple sclerosis herself, clearly and sharply conveys this disgust by stating, “I’m not, for instance, Ms. MS, a walking, talking embodiment of a chronic incurable degenerative disease.” (Mairs 13), and that she is actually, “the advertisers’ dream: Ms. Great American Consumer. And yet the advertisers, who determine nowadays who will get represented publicly and who will not, deny the existence of me and my kind absolutely”(Mairs 14). Mairs is greatly upset that disabled people are defined by their disabilities and, therefore, are underrepresented in public media. This might lead to one asking themselves, but why are they? And the answer, according to Mairs, is quite simple, “To depict disabled people in the ordinary activities of daily life is to admit that there is something ordinary about disability itself, that it may enter anybody’s life”(Mairs 14). Mairs concludes by pointing out how this effacement could have dangerous consequences for both disabled people and, as she called everyone else, TAPs (Temporarily Abled Persons) alike. Treating disabilities as an abnormal characteristic (as opposed to viewing them “as a normal characteristic, one that complicates but does not ruin human existence” (Mairs 15)) can cause one of these repercussions, as it makes the

Author of disability Nancy Mairs who’s a feminist and a cripple, has accomplished a lot in writing and teaching. Her remarkable personality shows in many of her essays especially in Disability which was first published in 1987 in the New York Times. In this essay, Nancy Mairs shows how disabled people are constantly excluded, especially from the media. By giving out facts and including her personal experiences, Mairs aims for making some changes regarding the relationship between the media and people with disabilities. Mairs thesis is shown implicitly in the first

The article “introducing disability Studies” by Ronald J. Berger was an eye opener in uncovering the past history of negative stigma associated with having a disability. Through history people have felt the need to stare at people with disabilities or to turn away in fear of maybe contracting the “disease”. This negative attitude was positively reinforced by ordinances such as the Chicago “ugly law” in which a person with physical deformities would have to pay a fine for simply being too “disgusting” looking to other citizens. This law was in place from 1880 to 1973, which is pretty recent in history. However there are positive glimpse in history when it came to uncovering and defining disabilities. Men like Leo Kanner and Asperger have dedicated

In 1817, the American School for Deaf was founded in Hartford Connecticut. This was the first school for disabled children in the Western Hemisphere. Although this was not the beginning of the Disability Rights Movement, it was a start to society, making it possible for people to realize that there were those with disabilities out there in the world and something had to be done. The Disability Rights Movement fought for equal access, opportunity, consideration, and basic human respect along with dignity for those born blind, deaf, or anyone with other forms of physical or mental disability. The purpose of social movements is to provide social change regarding a specific issue in which a particular group of

Usability is a critical portion of web design that one must be ever mindful of when constructing websites. Whether creating a personal web space or building multiple pages for a large corporation, it is the burden of the designer to guarantee people can access that content. According to the United Nations, disabled people compose roughly 10 percent of the world’s population (United Nations, 2010). Many regulations and standards have been set forth to provide disabled people with the same opportunities to access content available on the World Wide Web, as it is most of the World’s population.

The Americans with Disabilities Act was executed in 1990. It stated that the act is a civil right that forbids the discrimination towards anyone with a disability. Basically, no discrimination in school, work, etc. Disabilities such as a disability of vision, learning, mental health, or movement. Places of work used to not accommodate people, but now they must. People with disabilities were gainful from the ADA act. After the act was executed, people with disabilities, places of work were now required to do so. A lot people profited from the ADA it was helpful in many ways. The American Deaf community was a group who benefited from the ADA act. The issue with that is the Deaf community do not label themselves as disabled, but a culture. The

CUNY disability programming has grown in both size and scope, with our programs now utilized as models throughout the country. Though every campus provides services, each has developed a unique delivery model. ..... We introduce CONNECT, a new platform to share news, post events, and open our doors to the disabilities and higher education communities..

There is a controversy whether or not people who are obese should or shouldn’t be covered by the American with Disabilities Act.

In my essay you will learn about Jamaican and Haitian culture and their outlooks on disability. Laster on you will see the comparisons between those two cultures and the American culture. I selected the Jamaican culture because it has always been a dream of mine to visit Jamaica. I selected Haiti because I am not well educated on their culture.

ICF stands for International Classification of Functioning, Disability and Health. It views disability in terms of body functions and structures, activities, participation and important contextual factors, as stated in the ICF PowerPoint presentation (Francaviglia). At the top of the diagram, shown in the ICF PowerPoint presentation, the health condition is described as any disability, disorder, injury, or trauma, but also includes important conditions such as pregnancy or aging (Francaviglia). Moving to the next level of the diagram, the body structures may include the specific limb or organ deficiency, functioning defect, or impairment from the health condition. These body structures effect “the execution of a task or action by individual”

be protected by the A.D.A. this person must have a long standing record of this

It was warm that day. I walked to the bus with my hands shaking and eyes wide. I knew this was going to be a big day for me but I had no idea that Saturday would be the first day of the rest of my life. At first glance, this may seem like a big statement but my first day of volunteering with Camp A.N.C.H.O.R. (Assisting the Needs of Citizens with Handicaps through Organized Recreation) sent me on a journey with social justice that I am still taking. At 16 years old I thought I was going to go in and change lives but, the individuals I met ended up changing mine. I didn’t know what I was doing or much about the populations I was dealing with. However, I did know the individuals I was working with were incredibly funny, smart, talented, and had so much going for them except for one thing, their disability. I realized that these individuals were being portrayed as incompetent, unintelligent, and incapable because of one small aspect of their life. After speaking to some of their parents over the course of two years, I realized the immense difficulties these families go through. My initial reaction was anger, and then it dawned on me. If I want people to treat me like an individual and give me full human rights, have access to a public education, not receive discrimination during job interviews, they should have the exact same rights. This is not something they choose to take on each day. It is a part of their life that they deal with everyday as so many of us do with other

It doesn’t matter what you look like on the outside, it’s what’s on the inside that counts, but our society today lacks to understand that. In today’s time different is not accepted, people that are different are discriminated, looked down upon and usually picked on. People with disabilities are seen as different creatures by most people, the disabled don’t choose to be the way they are, but still our society alienates them. There are different types of disabilities, some type of disabilities are; mental disability, physical disability, learning disability and socializing disability. These disabilities are seen as weakness in our society that hence contribute to the stereotype that leads to the discrimination against the disabled.

In reviewing the required videos and reading on low incidence, there were a large range of how it affected individuals are processed by individuals without disabilities, these videos demonstrates what it is like to try to be normal with a disability. The first video called, Autistic Basketball Player,” presented an enlighten outcome, that people should not assume that individual with disability are not able to contribute to a job or sport. Jason Mcelwain’s a young man with Autism that id given to chase an individual with a disability self-worth is just as valuable as the rest of the team when it come to sport. The second video called, “Breaking Barriers of Autism: The power of Kindness and friendship present how individuals with disabilities are able to leap bounties id one person will acknowledge them. In his lecture he was able to present insight on how lonely it is on another side of the disability spectrum.

Chapter 7 was enlightening and the chapter I was able to relate with the most thus far. For example, one part of the text stated that educators and families often set low expectations for students with disabilities. I can relate to this personally. When I was in the IDEA program, my classes were rarely challenging and my teachers generally set low expectations for my peers and me. I believe the reason for this was to not stress the students or push them past their limits. However, my best teachers were those who did push me to my limits, so I could set a new limit the following semester.