Nancy Mairs On Being A Cripple Summary

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

She talks about the progression of MS throughout her life, and gives numerous examples of other people she knows who are also afflicted, and different ways she reacts to them. She ranges from the aforementioned two older women to another friend, Michael (243), providing her readers with a variety of people to identify with. Once she has them seeing themselves in the piece, they are also able to see themselves in her. By seeing the good and bad aspects of Mairs’

Mairs uses a high quality choice in words throughout the essay to describe her condition and herself as a person. In the passage she states that people “wince at the word cripple because they can't handle it .She also states that the other words that people would use to describe her don’t correspond to her condition. In the passage she quotes George Orwell’s thesis which states “the slovenliness of our language makes it easier for us to have foolish thoughts.” She agrees

In “On Being a Cripple”, Nancy Mairs, an American poet and essayist, describes her personal battle with multiple sclerosis, a degenerative disease of the central nervous system with no known cure. She begins with a personal account of falling into a toilet because she loses control over several motions. Mairs prefers to be called a cripple rather than a disabled or handicapped person, although she acknowledges that this is not the same as others’ preference. She explains her journey from being a young, active child, to losing control of her body and developing a blurred spot in one eye in her late twenties. As her body continues to break down, Mairs tries to stay involved by participating in activities like bridge and

Someone who is crippled often receives pity and sympathy from others, but do cripples always want this? In this passage entitled “On Being a Cripple,” Nancy Mairs uses interesting word choice, repetition, and a sarcastic tone to touch upon a subject that most mature non-crippled Americans are not entirely comfortable with; using the so widely feared word “cripple” instead of the common “handicapped” or “disabled” to be polite or politically correct. Elaborating to a society, so infatuated with being politically correct, that using a word considered derogatory to most may be necessary according to exact definition is Mairs’s purpose in writing this passage.

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

Additionally, Mairs continues to discuss the role of society in her struggle with multiple sclerosis. Though she has a relatively positive perspective of herself, Mairs admits that her self- perception often wavers not only because of the realities of MS, but also from societal pressures. “Part of the pressure arises from social expectations. In our society, anyone who deviates from the norm had better find some way to compensate.” Because of this, Mairs intends to be a “good cripple” and live life to the best of her ability. She recalls her adolescent conflict with self-alienation that was due to the influence of society’s version of an ideal woman, and how those feelings resurged in response to the devastation diagnosis of MS. “Like many women I know, I have always had an uneasy relationship with my body...the self-loathing I feel is neither physically nor intellectually substantial. What I hate is not me but a

In “On Being a Cripple,”  Nancy Mairs describes her life as a “cripple,” being treated different for her multiple sclerosis. She describes how society views her as handicapped or disabled both which are terms that the author dislikes.  Her viewpoint makes readers question their own beliefs on how the terms handicapped, disabled, or cripple influences a person to think differently about each term and its meaning. One of the reasons I chose this essay was because the author shows how different terms could affect the way society thinks about a person. Mairs believes that society often judge others based on their physical appearance and use the terms handicapped, disabled, or cripple to label. She argues that the outcome of this is creates an idea where being a cripple, or being disabled is considered a taboo where you're expected to be treated differently. Mairs claims that society i

C). Nancy Mairs keeps readers engaged by telling about everything that happened in her life. In addition, she engaged me by learning new information about her MS conditions. She describes the changes of her life from a normal life style since she was young until she become a cripple. The writer used reality examples and details that happened in every day’s life. For example, she has many sharp comments about

Mairs starts the essay by telling us about the incident where she became unbalanced and fell in the restroom, which led to her writing the essay. She admits to us how she fully accepts her disease and is not ashamed of it. She says, “ I am a cripple. I choose this word to name me.” From this, we can see that she wants people to identify

Even as Mairs still suffers, she has learned to handle herself in the face of adversity. She is forced to handle the fact that there is little that she can do to combat her condition. In contrast to her feelings at the beginning of her journey when she focused on the amount that her disease was ruining her life, she became able to not let that define her. She is aware of

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 and last

If you saw a person in the mall in a wheelchair, would you judge them? Or would you look at them like they are a normal human-being? People who have a disability whether they are physically disabled, mentally disabled, or learning disabled, are still themselves. Nancy Mairs was forty-three year old woman with multiple sclerosis. She wrote an essay, “Disability”, that explained her views of her physical disability.

In the essays “On Being a Cripple”, written by Nancy Mairs, and “Living Under Circe’s Spell”, written by Matthew Soyster, both authors strive to communicate to the reader what it is like to live with MS. Although both writers have a similar purpose, they both use exceptionally different methods of communicating their experiences with MS. Overall, Mairs’ essay proved to be more effective than Soyster’s, because of her varied use of rhetorical devices that all work together to create an effective argument. On the other hand, Soyster’s essay was less effective because he only relied on pathos to convince the readers of his argument.

Multiple Sclerosis, commonly known as MS is an autoimmune disease of the central nervous system. Scientists have been studying MS since the 19th century. In MS, the body’s immune system produces cells and antibodies that attack myelin in your brain which is essential for the nerves in your brain and spinal cord to conduct electricity to perform its function. The attack on myelin results in vison loss, paralysis, numbness, muscle weakness, difficulty walking, stiffness, spasms, and bladder and bowel problems. MS has varying degrees of severity and affects people between the ages of 20-50, mostly women. Although there are treatments, there is no cause and cure yet.