In American society, if American’s do not look the same as society’s ideal image, then they are not considered normal. Those non normal American’s are treated as if they have a plague and are left on the outside always looking in. The people who have something that sets them apart from the norm, such as a disability, should not be treated differently than the people who are society’s version of normal. In “Disability” by Nancy Mairs, the problem of judging a book by its cover discusses individual examples relating to people who have a disability. Mairs’ essay discusses having a disability in a world where disability is ignored, especially by the media. Television shows don’t show that people who have a disability can form their own decision. “[In Mairs’ essay] a woman with multiple sclerosis is portrayed on one of those medical dramas…She was terribly upset by the diagnosis, and her response was to plan a trip to Kenya…she got as far as a taxi to the airport…she succumbed to [her true love’s] blandishments …show more content…
For example, she wrote “…you might conclude that there is something queer about you, something ugly or foolish or shameful” (14). When American’s walk by people who have a cane or wheelchair, they probably don’t think “Oh, I want to be friends with them.” American’s probably think they’re a “cripple.” American’s don’t treat people who have a disability with respect. Instead, they judge a person who has a disability harshly. Leaving people who have a disability out of things and forgetting about them hurts their feelings. For instance, in Mairs’ essay she says “…you might feel as though you don’t exist, in any meaningful social sense, at all” (14). No one wants to feel that way, but people who have a disability go through it all the time. The media’s influence may convince people who have a disability to feel as if they’re an outsider since they have a “shameful” part of
Nancy Mairs Essay Crippled, handicapped, or disabled? Nancy Mairs describes herself as crippled even though many people who are disabled hate that word. In the passage Nancy Mairs discusses her view and opinion on the three words. Upon discussing the three words she uses tone, word choice, and rhetorical structure to enhance her claims. Nancy Mairs describes herself as crippled and she goes on to tell us that she “would never refer to another person as crippled.
In the essay “On Being a Cripple”, Nancy Mairs has multiple sclerosis and describes her life being a cripple. She talks about how the disabled is not accepted to society. She doesn’t want to be identified because she is disabled; she doesn’t want to be called “handicapped” or “disabled”. She wants to be named cripple but would never use it to call others. She feels as the cripple describes her the best, she doesn’t see herself as disabled or handicapped because she believe she is able to do things even though she have disease.
A disability can make someone look at a "disabled" person in a specific way, even though they are just as capable as others of doing things. Some people don't realize the impact someone with a disability can have on the world because they are limited and criticized for their issues. People without disabilities can show what they have, and those with disabilities will never even get past the starting line because of people's biased views on disabilities. After listening to the Ted Talk by Keith Nolan, a private cadet, he established ethos, logos, and pathos through his educational speech on the deaf in the military. In the Ted Talk, Keith Nolan backs up his story with emotion, statistics, credible information, and real-life experience.
Nancy Miers is a cripple, by her own admission, and in her essay 'on being a cripple' she uses humor and stories to show how she does not want to have her condition to hold her back in life and that people who are crippled can still lead full lifes if they can 'own' being crippled instead of being owned by
Nancy Mairs, a feminist writer who has Multiple Sclerosis, defines the terms in which she interest the most with the world. Nancy Mairs will name herself a cripple and not be by others. She will choose a word that represents her reality for example in the beginning of her story she mentioned about her being in the bathroom trying to come up with a story about cripples. She was in the handicap bathroom and when she tried to open the door she fell, landing fully clothed on the toilet seat with her legs splayed in front of her and she said “the old beetle -on-it’s back routine.”
One reason Robert Latimer gave for ended his daughters life was because he refused to subject her to further painful medical treatment or “mutilation”. In Peter’s view, it was Tracy’s able-bodied father who unilaterally decided that her disability was too much of a physical burden. In other words, his beliefs were based on his own reality as an able-bodied person, and not necessarily on the reality of his daughter’s life; his own bias led him to the conclusion that his daughter would rather die than live through another surgery. Peters’ argument is very important, as these biases would have troubling implications for people with disabilities, many of whom have had similar surgeries and consider it a normal part of their life and not as a catastrophe.
Nancy Mairs “Being a Cripple” focuses on her relationship with her disease that causes her to be disable. But her relationship to her disease can be complicated because she can’t escape from it and it interferes with her emotions causing her to feel depressed. Indeed, in the opinion of this essay, Mairs illness affected her physically and emotionally in her daily
Nancy Mair’s “on being a cripple “ is a self-reflecting story about her journey through a daunting illness. She puts forward her life before and after the diagnosis of MS. Nancy represents a powerful character who does not bow to challenges. She shows us that illness is no excuse to give up what you love. She has influenced the hearts of many and inspired so many handicapped individuals to pursue their ambitions.
Through all this work, Justin Dart came to the conclusion that the judgement towards disabled people created a toxic relationship disabled and abled individuals and decided to end this. In his explanation for why the ADA was so significant for the disabled, Justin said “It will proclaim to America and to the world that people with disabilities are fully human; that paternalistic, discriminatory, segregationist attitudes are no longer acceptable; and that henceforth people with disabilities must be accorded the same personal respect and the same social and economic opportunities as other people.” (Paragraph 7) The fact that at one point disabled individuals were treated with disrespect, really shows through this quote and emphasizes that this was a great injustice that needed to be ended. The injustice that occurred was that people with disabilities in America were treated poorly and did not have equal rights.
Reading an autobiography can supply valuable information about a person by revealing their narrative of personal challenges and successes. Michael J Fox wrote an autobiography about his challenges, including life with Parkinson’s disease. He fought a hard battle with alcoholism, depression, and family turmoil before and during the midst of his Parkinson’s diagnosis. In the beginning, he solely found solace in the bathtub trying to forget about his malady.
As an individual who developed a serious case of multiple sclerosis, Nancy Mairs begins to see herself in a different way, not as a normal person but as a “cripple”. As she opens with “I am a cripple.”. The disease ripped away her ability to walk. The disease allowed her to realize the deeper meaning of derogatory terms, such as “disabled” or “handicapped, especially the term “cripple”.
“Only 50 years ago persons with intellectual disabilities were scorned, isolated and neglected. Today, they are able to attend school, become employed and assimilate into their local community” (Nelson Mandela). Prior to the later part of the 20th century people with intellectual disabilities were often ridiculed, treated unfairly, feared, and locked away in institutions. According to Rhonda Nauhaus and Cindy Smith in their article Disability Rights through the Mid-20th Century, The laws of any nation reflect its societal values. The real life issue of discrimination towards people with intellectual disabilities in the United States and Australia is demonstrated in the novel, Of Mice and Men by showing how this issue affects one of the main characters, Lennie Smalls.
In “Unspeakable Conversations” she details her experience. Harriet McBryde Johnson effectively uses the rhetorical appeals of ethos and pathos, along with her uses of first-person narrative and descriptive language, to support her argument that contrary to stereotypes, a person living with a severe disability can live a happy and fulfilling life. Harriet McBryde Johnson was born in 1957 with a neuromuscular disease. At the time of this essay, she had been disabled for over four decades. Born to parents who both taught foreign language, they were able to afford hired help but she knew it could not be for her whole life.
In the passage that begins “I am a cripple.” by Nancy Mairs, she describes why she chooses to identify herself and only herself as a cripple. With Mairs tone, word choice, and rhetorical structure, she is able to clearly state why she identifies as a “cripple.” Initially you can tell that Mairs has a serious tone towards her writing with a very simple, clear, and effective opening statement.
Sexuality, self-image and identity formation are significant topics for all adolescents, including those with physical disabilities. For youth, gaining an understanding and acceptance of their sexuality plays a significant role in the development of identity and positive self-image, which are key developmental tasks during this stage of life (Rousso 1996; Schachter 2004; Van Damme and Biltereyst 2013). Having a physical disability may limit young peoples’ physical functioning, but it does not always affect basic physiological and sexual drives or their desires for love, intimacy, and affection (Milligan and Neufeldt 2001). However, research demonstrates that youth with disabilities are often excluded from these normative models of sexuality