Disability Reflection

The amount of people who live with disabilities is a controversial number. Depending on what law and diagnostic tools used, a person may have a visible disability, or one that may lie beneath the surface of his or her appearance. Some people believe that the term “disability” is merely a label use to hold back, or prescribe helplessness. Meanwhile, individuals who have been properly diagnosed with disabilities struggle to maintain respect and acceptance every day. In plain language, there is a lot of misunderstanding between people with disabilities and those without. It is firstly important to get everyone on the same page regarding the definition of disability.

“There's nothing more debilitating about a disability than the way people treat you over it.”( Solange Nicole) In today's God abandoning society there are many people voicing about equality. There are feminists, those against racism, those against homophobia, and those opposed to everything. Each group seems to have people standing up for them. Although when it comes to a group of cripples there's not many that can do the standing. Ableism: Discrimination in favor of able-bodied people. While many people don't know that word, or do not believe such a thing exists, there are many things proving that it does. It is easy to get caught up in life and not realize the difficulties people have, especially ones that could be easily fixed, just by

I have personally used labels when referring to students with a disability, and know that is something we, as educators, should be at the forefront to dissipate. Many of us have used phrases like “the girl with Down syndrome,” or “the autistic boy,” but when we do that we are labeling that person has something wrong with them, or that they are largely different that other people. Jennie Fenton likened that thinking process as asking someone “When did you find out you were bald? What is is like being bald? Do you have problems getting a job? Do you live at your parents’ house, or do you live in a home for the bald?” (TEDTalks, 2014). This thought process resonated greatly within me. I would never think to ask these questions or even feel the need to ask them to a person whom has less hair than someone else. So, why would I think or treat someone with a disability differently, or even believe they should be segregated or excluded from every aspect life has to

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

Disability is a topic viewed differently by each set of eyes. To truly understand a disability, one must live through it or frequently view the lives of another, struggling with an infirmity. Living with a disability may be hard, but it does not mean it is not worth living. Nancy Mairs, author of the essay “On Being a Cripple,” has written about her views and experiences, explaining to the public the truth behind being a “cripple,” and proving that disease does not control you. Explained in the paper, able-bodied people make assumptions to how low quality life must be, living with a disease and that these individuals are constantly unhappy however

Disability has functioned historically to justify inequality for disabled people themselves, but it has also done so for women and minority groups. That is, not only has it been considered justifiable to treat disabled people unequally, but the concept of

Disability in a socio-cultural context can be defined as "a barrier to participation of people with impairments or chronic illnesses arising from an interaction of the impairment or illness with discriminatory attitudes, cultures, policies or institutional practices" (Booth, 2000). The traditional view of disability often focuses on the individual, highlighting incapacities or failings, a defect, or impairment. This focus creates obstacles to participation on equal terms since an individual who seems to lack certain capacities may not be able to attain autonomy.

The two resources which I have chosen I feel reflect some of the contrasting models of disability which we have looked at in Units 1-4 of the course materials (E214, The Open University, 2010). The first resource comes from the National Autistic Society’s website and the second comes from the national newspaper The Guardian.

The interview with Darlene and Kristen has added to my knowledge about adults with disabilities that I did not get from part 1 and 2 of this project. One is how the disability could be more beneficial than hurtful to the person’s life. Like with Darlene, one can could be almost oblivious to the disability and hardship it can cause. This aids them in fully functioning in their lives without feelling hopless and frustrated in their situation. I also learned how fullying being a caregiver can be. Any job is frustrating sometimes, especially those you have to take home with you, but interviewing Kristen showed me that the love and enjoyment see gets from Darlene and Rhonda, her other client, is worth it. I also learned how a relatively short

Merely from knowing that a person is disabled they form wrong opinions about other unrelated characteristics of that person. Like people treat one who is mute as in they are deaf by talking in a high-pitch tone.

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.

When people have a disability it is life changing for them. They cannot just flip a switch and turn it off; most times it is a permanent ordeal. Participating in this experience opened my eyes even more to specifically what disabled people go through on a daily basis.

Over the years, perceptions towards disability have been significantly changing as result of the long pathway the disable community has taken fighting for Civil Rights, inclusion and against discrimination. Unfortunately, this last one has not been totally accomplished yet. Barriers to social integration still exist in the society. Perhaps the greatest barrier is not the disability itself; is the attitude of people.

Approximately 15% of the world’s population is, in a way, disabled. Whether it is a physical disability or a serious chronic disease, we have about one billion people in the world that live with a disability every day of their lives. It often occurs that these people are seen as an outcast of society; people that cannot live normal lives. It is important to realize that this is not true at all. People with disabilities are completely able to be part of the world. It is just the world’s duty to accept them.