Analysis Of Nancy Mairs Living Under Circe's Spell

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.

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 her essay, Mairs describes how society uses different terms to describe people’s appearance such as disabled, handicapped, and cripple. She claims that society’s poor use of language and meaning has resulted in the way society thinks on the terms disabled, handicapped, and cripple. An example of this is when Mairs uses the word cripple as she claims that people wince at the word when they hear it. She says the word makes her appear as a tough customer as she is want to been seen as someone who can face the harsh reality of her condition. Mairs argues “Society is no readier to accept crippledness than to accept death, war, sex, sweat, or wrinkles”(Mairs p.241) which states that society isn’t willing to acknowledge people with disabilities as they are put at a disadvantage. She also states that society doesn’t want to acknowledge the fact that a disability could potentially be worse than death as she uses her own experience to show her audience that the evil of humanity is not only death. She claims that society doesn’t take the issues of disabilities seriously as they treat those with disabilities differently rather than acknowledging them for who they are.

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

In Nancy Mairs short story, “On Being a Cripple”, she reflects on her life handling her disability of Multiple Sclerosis (MS) and how it has changed different aspects of her existence. She defines herself as a cripple despite the negative connotations the word may have. Over the past ten years, Mairs has had her MS slowly progress as her body deteriorates. She sees her life as fairly average, but seemingly small tasks have become difficult to her and has required help from her family. Despite their support, Mairs still fears that people's kindness is out of pity. The stigma around physical disfigurement and being crippled causes added suffering to her life. Although the disease dictates much of her existence,

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 novel Rules by Cynthia Lord, I think the author is addressing the frustrations people experience in the face of disabilities. In looking at tone, in Rules we are interested in how the author feels about his or her subject.

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.

My Left Foot has many great examples of characterization that show the emotions of disabled people. Christy explains that he is there in mind, but not in body when he says, “Slowly, patiently, penetrating beyond the thick curtain that hung over my mind, separating it from theirs. It was hard, heart-breaking work, for often all she got from me in return was a vague smile and perhaps a faint gurgle.” (Brown 237) The use of

For instance, both Flowers for Algernon and Awakenings include themes towards the treatment and respect of those living with mental and physical disabilities. In Flowers for Algernon, Charlie was unknowingly used as a punchline by his supposed friends and colleagues at the bakery, merely because he was mentally challenged and the incompetence that resulted from this made others feel superior to him. Following the surgery and the increase of Charlie’s intelligence, the doctors insinuated that he wasn’t considered a human being prior to the experiment. They implied that those with impaired mental abilities are not individuals capable of independent thought and feeling, which is disproved through Charlie’s progress reports. Similarly, Awakenings sheds light on the treatment of those who have physical challenges, in the manner that the nurses and doctors treated the patients before the medicine was administered. They are visibly reluctant to tend to the patients, and attempt to avoid work with television shows because they lack compassion and understanding towards their conditions. The staff thought efforts to help them were futile due to their catatonic states, therefore neglecting them, treating them like obligations rather than individuals. However, both stories show that in spite of their circumstances, those with disabilities are not lesser people and are deserving of compassion and respect just as others are; though they are often ill-treated and misunderstood.