In The Memory Book by Lara Avery, Samantha has always been socially awkward; however, after getting diagnosed with Niemann Pick Type C, she becomes insecure and unconfident. Niemann-Pick Type C, or NPC, causes her to experience memory loss, incoordination, blackouts, and other symptoms. To cope with her disease, Samantha starts writing in a journal in order to remember important events and memories. However, her closest friend and debate partner, Maddie, starts to drift away after learning about her disease. Samantha is in a similar situation with her boyfriend, Stuart, when they start having problems after she informs him of her disease. Critical Disability Theory examines of the representations of people with disabilities throughout literature …show more content…
First of all, Samantha comments on her outfit while dressing for a date:“This is an outfit that says, ‘I am just a normal, ambitious, laid-back young woman who does not have a debilitating disease.’ Right?” (144). When Samantha says she wants to look “normal” she gives her disability a negative portrayal, saying she wants to hide her disease from the public. This suggests that she denies the fact that she has a disease, representing disability as shameful or disreputable. When Samantha says a “normal” person cannot have a “debilitating disease”, she marks disabilities as undesirable or non-normative. Furthermore, Samantha describes her disability as “debilitating”, contributing to the stigma that people with disabilities are helpless or weak. The adjectives “ambitious” and “laid-back” are both associated with “normal” instead of her disease, giving the impression that people with disabilities are lazy or lethargic. Additionally, Samantha overthinks a text from Stuart before her date:“Oh god, he said, ‘See you in a bit.’ Okay, I will see him in a bit. I will see him in a bit for the second date of my entire life and perhaps the last because watch me forget my own name. Watch me enter the Canoe Club and everyone I know is there, like an intervention” (144). Avery employs anaphoras throughout the quote to demonstrate the overthinking that occurs in Samantha’s thoughts. One example of this is “See you in a bit”, the text sent by Stuart that she repeats in her head. This gives off a rambling effect that develops into a nervous tone, seen throughout the paragraph. This anxious tone indicates that although going on a date in general can be stressful, her disability adds another layer of anxiousness. Additionally, she states, “watch me forget my own name”. This demonstrates that she is nervous because of her disease, and fears that her disability will be the
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 the book, The Short Bus, Jonathan Mooney’s thesis is that there is more to people than their disabilities, it is not restricting nor is it shameful but infact it is beautiful in its own way. With a plan to travel the United States, Mooney decides to travel in a Short bus with intentions of collecting experiences from people who have overcome--or not overcome--being labeled disabled or abnormal. In this Mooney reinvents this concept that normal people suck; that a simple small message of “you’re not normal” could have a destructive and deteriorating effect. With an idea of what disabilities are, Mooney’s trip gives light to disabilities even he was not prepared to face, that he feared.
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.
In Nancy Mairs ' "On Being a Cripple," she deliberates the relationship between the English Language, American Society, and her struggle with multiple sclerosis (MS). Mairs criticizes people for wincing at the word "cripple," and using terms like “differently abled,” because they lack reality and accuracy. She equivalents society’s inability to accept crippledness with death, war, sex, sweat, and wrinkles. Through the usage of ethos, pathos, logos and other rhetorical devices, she effectively tells her story and proves that there is power in words, from which she could come to terms with a new fact of her identity, and to accept the incurability of her disease.
The societal expectations for beauty are an ingrained concept amongst the minds of almost every individual, who in turn project these standards on each other and their own children. Throughout her adolescence, Walker seeks for validation of her beauty through others. “When I rise to give my speech I do so on a great wave of love and pride and expectation.” (Walker 2). Walker was seeking a reaction from her audience as she read her Easter speech to her church; a reaction of approval and admiration, which then confirmed her “cuteness”. The emotional toil brought upon by the accident caused Walker to go into a dark place of unacceptance of herself. She did poorly in school, was bullied in school, and kept her head down for several years of her life because of the shame she felt from the appearance of her eye. “I tell it I hate and despise it. I do not pray for sight. I pray for beauty.” (Walker 5). At twelve years-old, Walker talks about the eye that has gone blind and development of her self-unacceptance can be seen here. The lack of concern she had about the function of her eye, but rather the aesthetics, shows how dependent Walker was on in achieving societal standards.
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
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 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.
She shows herself as cowardly when she was reeling after the accident, “For six years I do not stare at anyone, because I do not raise my head.”(444), she says, portraying her disgust for herself. Walker utilizes the tone of her writing to manipulate the progression of her attitude shift. For instance, in the stages soon after the accident she uses a very morbid and pessimistic tone to describe the events that are transpiring at that juncture of her life. Stating, “I do not pray for sight. I pray for beauty.”(445), proving that even though this accident has occurred she has still remained very resistant to a change in attitude. She also couples detail to multiply the effect that these strategies have on the reader because when she describes these events, the details she uses reflects the tone, so it visibly transmits the idea of her attitude at that phase, which would be much harder to achieve without these rhetorical techniques used appropriately. The dialogue also plays into this idea as well as it also reflects the current mood of the stage. For example, when she was still very young she used very flattering words as dialogue to complement the tone where she thought beauty was everything and being most beautiful was most important. “That girl’s a little mess.”(442), “And got so much sense!”(442), people bombard
In Alice Walker's “Everyday Use” she uses a tactic to set a mood for the reader by bringing in the character Maggie. Walker's use of language when describing Maggie creates a picture of a physically scarred and unintelligent girl. Maggie's physical scarring is pointed out
Unlike Dee, Walker’s description of Maggie is seen as an unattractive and awkward girl. Her mother notes “good looks passed her by” (355). Furthermore, she carries herself with low self-esteem, “chin on chest, eyes on ground” (355). Besides her appearance, when Maggie is first introduced in the story, Mama points out that she is nervous about her sister’s visit and “will stand hopelessly in corners, homely and ashamed of the burn scars down her arms and legs, eyeing her sister with a mixture of envy and awe” (355).