Wait a second!
More handpicked essays just for you.
More handpicked essays just for you.
Cognitive disorder
Cognitive disorder
Don’t take our word for it - see why 10 million students trust us with their essay needs.
Nancy Mairs’ “On Being a Cripple” is centered around a teacher/writer with a psychocentric personality that chooses the synonym cripple as the way to define her chronic degenerative disease called multiple sclerosis. Also she takes you on her personal life journey, which is plagued with challenges, depression, realizations, joy, hatred and acceptance of the disease. Mairs’ hates the way society views physical appearance and abnormality. Mairs’ has a distinctive concern about the language used in regards to this disease. She doesn’t like the word disabled, handicapped or differently abled because these euphemisms cause people to view her as something that she isn’t. Mairs’ states that “society is no readier to accept crippled-ness than to accept …show more content…
She was not good at sports, but like to climb, skate and ride her bicycle and sail. She hated sports due to humiliation with field hockey and basketball. The initial symptoms began when she was twenty-eight years old and she started to rip and drop things. A neurologist was contacted and determined that it was a brain tumor. A year in a half later, she developed a blurred spot in one eye. She was diagnosed with multiple sclerosis. Multiple sclerosis is a chronic degenerative disease of the central nervous system, in which the myelin that covers the nerves is somehow eaten away and scar tissue for multiple sclerosis in its place, interrupting the nerve’s signals. This disease has an unpredictable and uncontrollable course which leads to the loss of vision, hearing, speech, the ability to walk, control of bladder and bowels, sensitivity to touch, vibration and pain, potency and coordination of movements. The list of possibilities is lengthy and horrifying. Ten years from her initial diagnosis, she sustains some losses. She has sudden attacks called exacerbations followed by remissions. Her left leg is weak and she walks with the help of a brace and cane. She now uses an electric wheelchair. She no longer has much use of her left hand and her right side is getting weak also. There are some harsh realities that Mairs’ has to face regarding this
Disability they have, but styles to tell are more of difference. Nancy Mairs and David Sedaris use writing to address their disability in different ways. In both Nancy Mairs “On Being a Cripple” and David Sedaris “A Plague of Tics”, both authors describe and live with their disabilities in different ways. Mairs uses her familiarity to address the reader where Sedaris recollects his habits in a somewhat humorous way. Even though both have a disability it’s conveyed in two different ways. Mairs comes straight out the gate as being cripple stating “First, the matter of semantics. I am cripple” (Cohen 259). From this point on she goes on to explain her disease which gives you an idea of what’s to come. Sedaris approach is very different as he jumps into examples throughout his childhood and never states his disability. His habits are explained as “tics” while he uses his childhood experiences to describe his disability.
Due to this disease the body is slowly broken down by affecting the central nervous system of a person’s body. The children depicted in the essay are probably an example how fellow human beings should be around a disabled person. They just view the disabled person as another human being and respect them the same way. The children are proud to associate themselves with Mairs and do not shy away from introducing her to the general public. This is what a disabled person requires: that all those around him or her should respect them for what they are and give them unconditional regard
The fact that Mairs turns out to react counterintuitively to her multiple sclerosis is a curveball for the reader especially due to this question. As the reader has already pondered their response and rationalized it, the fact that Mairs goes against the status quo is a big element in her essay. Mairs’ technique was very effective and definitely superior to Soyster’s as she crafted it with more precision and had a structured setup for
As human beings, we like to make sure never to offend or judge anyone. We even have sayings like “never judge a book by its cover”. A metaphor that is often said whenever trying not to judge someone based on their outward appearance; however, it is not often that people practice what they preach. We judge people based on external factors within seconds. Even though we know what people see on the outside is not a defining factor or who we are as people. Nancy Mairs, author of On Being a Cripple, has to live through this every day. She knows this truth very well, and lives proudly with the fact that as she is disabled. Mairs is admirable for choosing to call herself a “cripple” and not be ashamed of it. Though the word is derogatory and a word that is avoided by society, Mairs identifies herself as a cripple because that is what she is. In explaining her disability, she says, “I haven’t always been crippled, ... to be whole of limb is ... infinitely more pleasant and useful. and if that knowledge leaves me open to bitterness … the physical soundness I once enjoyed is well worth the occasional stab of regret” (Mairs 186). What really
MS causes a degeneration of the myelin around axons due to the killing off of oligodendrocytes, which are cells that make up the myelin sheath of an axon; losing myelin decreases the neuron’s ability to propagate an action potential. Since this disease affects the central nervous system, MS can cause dysfunction of both the sensory and the motor aspects of the body. Some common sensory complaints(Lundy-Ekman, 2007) of MS are tingling, numbness, and/or paresthesia in the affected area, which is variable but typically involves one or more limbs (Palace, 2001), as well as partial blindness in one eye, a decrease in vision acuity, and double vision. Lhermitte’s sign, which is a radiating shock that travels down the back or limbs, is another common characteristic of MS that aff...
In her essay “On Being a Cripple,” Mairs describes her path of acceptance of her multiple sclerosis (MS) diagnosis by declaring that she is a “cripple” in alternative to the more broadly acceptable terms: disabled or handicapped. Her essay is written with humor, satire, an open heart, and open eyes. Mair’s purpose is to describe her acceptances of her condition by using rhetorical elements and appeals, such as ethos and pathos, in order to allure her audience.
As for this concern Connie Panzarino was born in 1947. She was writer, activist and artist with the rare disease Spinal Muscular Atrophy Type III, formerly called Amytonia Congenita. From her early stage filled with joy and pain in her every step in her life. Finally, she strove to define herself: "I knew I was different. She didn’t understand if that meant that I would never walk. She didn’t know that most children with this disease die before they're five years old." In this deeply moving and articulate memoir, Connie Panzarino gives explanations her decades of struggle and triumph. She filled with spirit, passion and insolence, The Me in the Mirror reveals the story of a remarkable life. How she affected name of gender and she affected the name of disability. How she strives for the identity in the patriarchal and discriminated world. I am going to explore the all this issues through this
In “On Being a Cripple,” Nancy Mairs. She hates to call her handicapped because she believes that hold her back. The author writes, “I certainly don’t like “handicapped,” which implies that I have deliberately been put at a disadvantage, by whom I can’t imagine (my god is not a handicapper general), in order to equalize chances in the great race of life” (21). In other words, she doesn’t want to call her handicapped, because she wants to live her life with equal chances even she’s not. Her positive attitude makes her more active. She’s trying to live a normal life with her disability. She hates being crippled, but she’s trying to get over it. If she had a negative attitude, she wouldn’t write about her own story. She wouldn’t do anything. I believe her positive mindset affects somehow to get rid of something that hold her back. She overcame the effects of her illness through positive attitude. Mairs and Jamison’s thoughts they have shaped their lives either positive way or negative
"On Being a Cripple" is an autobiographical essay by Nancy Mairs. The author was diagnosed with multiple sclerosis in her late twenties, and has since then lost full use of several limbs. Despite the stigma around the use of the word, Mairs refers to herself as a "cripple". With the use of this word she attempts to accept the reality of her situation without feeling sorry for herself. The author also demands the same of her readers and the people that she meets in her life. Mairs writes to those who wish to learn more about what it is like to live with this debilitating disease and how people react to it. She uses this essay to make a point about how society labels people while telling her story in a manner which cites examples from her life. She describes her life through everyday situations that occur when living with MS. Mairs does not have the same physical abilities that most of us don't think twice about, but she carries on with her life without the need for pity or a new vocabulary that attempts to make her condition seem less severe.
...ive most of their life as a perfectly able-bodied person until a tragic accident one day could rob you of the function of your legs, and you have to learn how to cope with being disabled. Mairs illustrates that being disabled is more common than the media portrays, and it’s hard to deal with feeling alienated for your disabilities. These three authors have evoked a sense of sympathy from the reader, but they also imply that they don’t want non-handicapped people to pity them. The goal these authors have is to reach out to the able-bodied person, and help them understand how to treat a disabled person. The disabled people don’t want to be pitied, but they still need our help sometimes, just like if you saw someone with an arm full of grocery bags having difficulty opening their car door. They want us to accept them not as a different species, but as functional people.
She told her readers that she has a muscle-wasting disease and she could only move three fingers on her right hand. She wrote that the reactions she got from most people were “Decidedly negative” (Johnson p.98) She wrote that she would hear thing such as “I admire you for being out; most people would give up.” And “You don’t let the pain hold you back do you?” (Johnson p.98) There is often talk about how popular culture teaches people to both see and not see the people with disabilities. Comments such as these are an example of such blindness. When a child sees a disabled person a parent’s first reaction would be to tell them not to stare. We teach children that it is impolite to be curious about people who live life differently than others. We carry the “its-not-polite-to-stare” idea into adult hood therefore when we come across a disabled we try not to make eye contact not as if we are being rude but because we are taught that it would offend them. All curiosity and attempts to understand are shut down at a young age for fear of offending someone. Therefore, any attempt to encourage is met with a deep misunderstanding of how the life of someone with disabilities truly works. Just because a person has a disability does not mean they are incapable of enjoying
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.
Mairs describes her condition and how it relates to the actions and responses of other people in any situation. Mairs uses the term cripple loosely, making sure it is not offensive to anyone. By starting her passage with, “I am a cripple,” Mairs doesn’t hide anything. She begins by coming straight out into the open with who she is and how she wants the world to view her. In the first paragraph, Mairs uses the word choose three times to establish her personal decision to be titled a cripple.
Multiple Sclerosis (MS) is one of the most common diseases of the Central Nervous System (CNS) which affects all ages and gender. MS is currently the leading cause of disability in young adults and found to be more prevalent in women and affects 2.5 million people worldwide. “Multiple Sclerosis is a progressive chronic immune - mediated disease characterized by disseminated demyelination of nerve fibers of the brain and spinal cord” (Mahan, Escott-Stump, 2008).
As Mairs wrote: “The fact is that ours is the only minority you can join involuntarily, without warning, at any time.” Looking at the issue from this angle, it is easy to see that many disabled people were ordinary people prior to some sort of accident. Mairs develops this point with heavy emotional appeals, arguing that the media, and therefore the population, do not see the disabled as ordinary people.... ... middle of paper ...