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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.

In her essay “On Being a Cripple”, Nancy Mairs presents her audience with an honest inside view of her life and perspective as a cripple, a word she openly uses to define herself. She brings her world to us by discussing a wide variety of things including language, family, and humor, and how these all relate to her life. Through various stories and insights, she allows her readers to gain an understanding and acceptance of people with disabilities. She examines the public’s view of the disabled, as well as the views they have of themselves, and compares them to her own. She makes it clear that she is not to be defined solely by her disability. In discussing honestly her views, as well as

When my older sister, Molly, was ten years old, she was a temporary cripple. Molly went through a pretty big surgery that would stop her from tripping over her pigeon toed legs. While living a couple months in her wheelchair, an uncle of ours came to visit. His warm welcome to my sister was pushing her into a corner, locking her wheelchair, and calling her a windowlicker. Thankfully, my sister has tough skin. She took what others would find scarring, all as a joke. It is hard not to be reminded of the unexpected response my sister gave while reading the essay “I AM a Cripple” by Nancy Mairs. Within this essay, the author describes her life as a cripple suffering with MS. While sharing her thoughts and emotions (gerund) from

Humans are social creatures. We identify ourselves through our community, loved ones, and those who genuinely appreciate our presence. Our identity defines our personality traits, highlight social roles. Those with disabilities are often confused about their identity because they are misunderstood and stigmatized. Through the use of literature, one can empathize better with other people especially those who are misunderstood by society. Disabled people are more likely to be neglected and subjected to prejudice or discrimination. In “Delusion of Grandeur”, Terry Ann Thaxton, talks about the struggle between Adam and his mother because of his disability. Adam struggles to cope with his environment and finds himself isolated and misunderstood. Families ultimately suffer but through their experience, they can learn some amazing lessons.

Those with disabilities have to accept their lives as being deprived of some joyful instances that may never happen. Individuals with handicaps may not be able to be active with their (or other’s) children, dream jobs may not be within grasp, memories may not be accessible while other’s take them for granted and shun those who desire that which they’ve already acquired (“People With Disabilities”). Provided, life is hard with a disability but additionally, those with handicaps must suffer isolation which is unfavorable in multiple ways. With isolation the person has no help, no support, no companionship, and feel ultimately rejected shutting them down in a social manner (“People With Disabilities”).

Who else can there be? Helen Keller, the amazing author who was both blind and dead at 19 months old. She lives most of her life struggling and stressing out, not being able to do much. She was the first disable person to graduate school and even received a Bachelor of Art Degree. But she didn’t do it all alone. Her teacher, Anne Sullivan, contributed to her success. She taught Helen the manual alphabet, hand writing, and other forms of communication and understanding,"I learned to spell in this uncomprehending way a great many words, among them pin, hat, cup and a few verbs like sit, stand and walk. But my teacher had been with me several weeks before I understood that everything has a name.” Anne and her husband helped Keller with her first book, the autobiography, “The Story of My Life”. After her success, she wrote more books and inspired other disabled people to do things in life and paved a path for

I was taken back by how often I had to give verbal cues as to the condition of the road or sidewalk. In a place like old town, which is considered a historical landmark, Americans with Disabilities Act (ADA) regulations are not usually employed, so for a person with a disability this can be challenging to navigate as the sidewalks are narrow, unbalanced and obstructed. Every bump and crack in the road is a tripping hazard to someone whose vision is impaired. Keeping my patient from running into people or telephone poles and when to step up and down curbs was a task. Several times I had to walk behind her because the two of us could not fit side by side on the walking paths. In addition to the extremely slow walking pace we had to maintain to avoid falling, I would forget she could not see what I could see and kept telling her to look at this store or sculpture, she then would remind me she could not see it so I would then describe it to her or take her to the item so she could feel it for herself. Another thing I noticed is the amount of attention you suddenly get as strangers watch you with curiosity, whereas they would normally probably never have given us a second glance if we were not portraying a person with impairments. One concerned onlooker did approach us as we were going down uneven

The mainstream press today when discussing a disabled celebrity disregards many of the persons accomplishments throughout their life, but instead focuses and finds themselves becoming more and more susceptible to drawing attention to their disability alone. Charles A. Riley II enlightens the able-bodied community on many issue’s throughout his book, “Disability and the Media: Prescriptions for Change.” He argues that the media is inaccurately depicting the disabled community throughout the use of advertisements, but may also be unintentionally disrespecting the community as well in face-to-face contact. Riley is a professor of journalism at Baruch College, and throughout his career, has received multiple awards for his writing’s on issues relating to disability. In Charles A. Riley II excerpt from “Disability and the Media: Prescriptions for Change”, Riley argues for a change from the media’s perception of disabled people, as a whole, due to how they are portraying celebrities within today’s media throughout the use of ethos, logos, and pathos.

It also gets hard for Mairs and she gets angry when she feels like society makes people with disabilities seem that they aren’t normal. In the essay Mairs mentions how in today's’ society the ideal woman is a beautiful physically attractive woman with no disabilities. “She is trim and deeply tanned; she jogs, swims, plays tennis, rides a bicycle, sails, but does not bowl . . “(57). Mairs says this to say that in today's society you’ll never see a crippled person in a magazine because it isn’t attractive or amusing to others and when society sees people with disabilities; they automatically think that they should feel sorry for them.

He states, “Our nation cannot tolerate discrimination of any kind” and “…to give the disabled access not only to buildings, but also to every opportunity in society”. The first quote appealed to our morality in a way that reminded us to uphold our nation's idea of fair treatment for all. The second quote enforced the idea of the former quotation but also prompted Americans to recall their obligation to help those with disabilities reach goals, such as employment, that they would not be able to achieve on their own. In other words, through his effective use of ethos, Reeve reinforced his belief for equal rights for all United States citizens living with a

Displayed in the media to this day are people shown with disabilities. These people are wrongly perceived by society as heroes or sensations. Instead of focusing on that, we should focus on how they are able to overcome the disability during their daily lives. A very trusted author and professor of journalism, Charles A Riley, wrote a book called “Disability and the Media: Prescriptions for Change”. After carefully analyzing this text from Everything’s an Argument, it is clear that Riley wants to adjust the way society views people with disabilities. He is against the fact that people with disabilities are not known for who they really are. I agree with Riley’s stance and can feel what he is expressing throughout his text.

I was born with Amniotic Band Syndrome, which is a Congenital Limb Deficiency. I wear a prosthetic on my right arm every day. The word “disabled” implies that a person is limited in movements, sense, or activities. I have never considered myself to truly be “disabled”, but I do believe that I am the person that I am today because of the barriers and challenges that I have overcome due to my physical limitation. Growing up, there was always a physical difference between myself and my peers. Many children wanted to put me in the category as the “girl with one arm.” I have long strayed from that label, but I continue to struggle with the relationship between my own identity and how I am perceived within society. “When someone who cannot see is labeled a ‘blind person,’ for example, it creates the impression that not being able to see sums up the entire person. Reducing people to a single dimension of who they are separates and excludes them, marks them as “other”, as different from “normal”(white, heterosexual, male, nondisabled) people therefor as inferior.” (Adams, 2013, p.15-21) Now that I am older, most people I meet do not seem to describe who I am solely based on my physical difference. This was always my biggest fear, I never

People with disabilities often feel like a burden in society, much like Lennie in the novel. With strict standards set by society of beauty and

Furthermore, school is a place where you make friends and integrate with one another. However, individuals with disabilities are often susceptible to face vast number of stereotypes, labels or discomfort at school. That is because of the lack of consciousness and biases that is created by imposing a distinction between non-disabled versus disabled from an early age. Valerie Piro tells us that some her classmates told her that she has a “perfect personal essay topic” (Piro 3). Her friends imply that she has the “perfect essay topic” because of her disability. Yet, it is rather confusing that they are being ironic, jealous or making fun of her situation. As Piro emphasizes, human beings need to “encourage one another to demand that society accept”

This week’s discussion dealt with Individuals and Disabilities. Over the years, people who have a “disability" have been subjected to prejudice and more. And the first way to diminish someone is through language, by using words or labels to identify a person as "less-than," as "the others—not like us," and so forth. Once a person has been identified this way, it makes