Miriamne Ara Krummel's 'Am I MS?'

Let me start off by explaining what MS is. Multiple Sclerosis is when, for reasons scientists are not yet sure of, a person’s immune system attacks the myelin that covers and protects the spinal cord and nerve fibers in your brain. After the myelin is damaged, the nerve fibers then are attacked by the immune system as well. This causes nerve damage, fatigue, vision loss, poor balance, and more unpleasant side effects. Multiple Sclerosis itself isn’t necessarily the cause of death, however, it 's the complications of MS that take a great toll on one’s health.

Even though she was diagnosed with Multiple Sclerosis, she is still able to have the strength to achieve anything that is possible to her. Because of having MS, the unpredictable course of the disease were terrifying to her. Each night she would get into bed wondering whether she will ever get out again the next morning. Whether she be able to see, speak, to hold a pen between, knowing that one day might come. With the horrible situation in Nancy's life she had the strength to overcome any obstacle.

Fittingly, she gets her own insights and the exchange with different sclerosis. By technique for individual stories, ethos is used to make the peruser grasp where she is starting from, so she can be seen as more dependable. Various sclerosis has emphatically affected Mairs ' step by step life, and she comprehensively clarifies especially how. Her symptoms of MS are an astonishing deficiency in her got out leg and hand, blind spot in the eye, and increases, or sudden strikes. Various are charmed to see how standard life still proceeds regardless of the various reactions the disease passes on.

Nancy Mairs, the author of “On Being a Cripple”, suffers from Multiple Sclerosis, a degenerative neurological auto-immune disease. In her essay Mairs writes how in the end her life did not really change all that much. In fact aside from banging around the kitchen a little more often and being slightly more clumsy, her life was just great. Her family was supportive, and she was able to easily come to terms with her disability, she was able to move forward with her life needing only minimal adaptations. And that is just great.

This quote shows that even though Mairs sometimes has difficulty accepting her illness, she knows that there is a growing acceptance of people who must deal with the difficulties that she faces. This ultimately lends a hopeful and positive tone to an otherwise serious and depressing section of her essay. This contrast in tone, but general feeling of hope is key to the type of emotions that Nancy Mairs is trying to educate her readers about. Mair is successful in using multiple rhetorical strategies to connect with the reader.

The poet successfully illustrates the magnitude with which this disease can change its victim’s perspective about things and situations once familiar to

(Digital Sport News, 2) Kayla Montgomery, a runner with MS, a disease that can disrupt and block nerve signals that go between the brain and lower body, is happy when she runs because she feels safe from her disease which is an obstacle in her

In the essays, Carnal Acts, Nancy Mairs, a young writer who deals with MS disease and mental illnesses speaks out about the difficulties of dealing with MS and how her voice as a writer helped her cope with the difficulties of MS. Mairs tells us she sees a very close connection between life and writing, “For me, thinking about literature and thinking about life aren’t separate, or even separable, acts (4)”. The theme of love who you are is distinctly depicted by Mairs in her essays. This theme is very common throughout the book, especially in the essay titled “Carnal Acts” where she clearly states society 's standards for women are too high. Mairs never considered herself beautiful because she never fit the perfect image of a beautiful woman,

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.

I don’t have time for BS.” - Neil Cavuto. In “On Being a Cripple,” Nancy Mairs discusses the language of American society while including personal accounts of her struggle with multiple sclerosis (MS). Mairs presents herself as a proud individual through her utterly defiant personality, her word choice in deciding to identify as a cripple, and explaining why other socially accepted euphemisms do not define her. Mairs makes it clear that she is a cripple and only wants to be identified as one by stating that “Whatever you call me, I remained crippled.”

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

Fisher begins her speech to the Republican party and struggling families by discussing how widespread the struggle of silence is for those infected and her own experiences of being shut out due to her disease through the use of a metaphor. In which she employed a serious tone appealing to the emotions of those affected by the disease when saying “I asked the

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”.

When a patient is told they have a disease, they are shocked. Some patients worry that they may die, and others feel numb or confused about it. They may have a hard time realizing that their disease could be fatal. “When he asked if she was okay, her eyes welled with tears and she said, “Like I’m always telling my brothers, if you gonna go into history, you can’t do it with a hate attitude. You got to remember, times was different” (Skloot 276).

The narrator is certain she is really sick, and not just nervously depressed as diagnosed by her husband, but she is confined by her role as a wife and woman, and cannot convince her relatives and friends that something is actually wrong with her. In the story the narrator says, “”If a physician of high standing, and one’s own husband, assures friends and relatives that there is really nothing the