Cycle Of Hope Analysis

In her essay “On Being a Cripple”, Nancy Mairs presents her audience with an honest inside view of her life and perspective as a cripple, a word she openly uses to define herself. She brings her world to us by discussing a wide variety of things including language, family, and humor, and how these all relate to her life. Through various stories and insights, she allows her readers to gain an understanding and acceptance of people with disabilities. She examines the public’s view of the disabled, as well as the views they have of themselves, and compares them to her own. She makes it clear that she is not to be defined solely by her disability. In discussing honestly her views, as well as

As of 2011, it has been reported that there are 650 million disabled people in the world (“Disabilities”). Though this number is high, it is greatly underestimated because disabled people are commonly isolated and stigmatized by their community (“Disabilities”). After hearing of this extremely high number of disabled people, I then ultimately decided I would write my research paper on ways to help the disabled. Therapeutic riding has been actively helping individuals with disabilities for decades, and can benefit these unfortunate people physically, mentally, and emotionally. “Therapeutic riding, which originated in Europe, has been actively helping individuals with disabilities since the 1950's” (Shepard). Through equine-orientated

People with disabilities are not completely gone. They are still there and have a mind of their own. They feel emotions and sometimes have a more complex mind than others. Two authors help enlighten this idea that disabled people are much more than helpless bodies. Both Christy Brown and Jean-Dominique Bauby perfectly illustrate their lives and what it is like to be disabled, and they prove by their stories that they think and feel, and can even develop enough to share what they feel with the world. My Left Foot is about the journey of a boy suffering from cerebral palsy. His entire life he was labeled as a loss cause by doctor after doctor, but his mom never gave up hope. Slowly, he started showing signs of development by random movements responding to certain situations. In the end he ends up being able to communicate with his left foot. The next story, The Diving Bell and the Butterfly, is about an individual who suffered a stroke at the age of 43, leaving him paralyzed, only able to blink his left eye as communication. He develops his own alphabet inspired by the French language in order to exchange conversations with others. His thoughts in the story jump from the present, him currently disabled, and the past, when he was not. Both memoirs, with very different stories, show the lives of two individuals that are not like others. One who had their disability since birth, and the other who obtained one after a tragic event. In My Left Foot by Christy Brown and The Diving Bell and the Butterfly by Jean-Dominique Bauby, both authors use characterization to show readers the struggles of disabled people and help them understand that just because they can’t use motions such as hand gestures to express how they feel, doesn’t mean that they don’t think and feel.

Growing up with multiple sclerosis for close to twenty years by the time she wrote the book, Nancy looks at the world the same way a child learning to walk does. She has enough reasons to believe she is uniquely privileged as a person with a disability. In as much as she misses activities like hiking, dancing and cycling, she thinks she is safer being unable to carry them out. This is in

Everyone has their own way of achieving victory: scoring the winning point in a sport, getting chosen for a job or acing a test in school. A writer for Sport Illustrated's, Rick Reilly, tells Ben Comen’s story, a teenager with cerebral palsy who runs for his high school’s cross-country team, in his article “Worth the Wait.” In the article, Reilly informs the audience of the previously mentioned situation that Ben is in, while also mentioning Ben’s process of overcoming all odds and managing to finish the races with the entire crowd cheering him on. Reilly establishes a triumphant tone with the aid of pathos and arduous-like diction to make light of people with cerebral palsy and to show how they can accomplish goals in life like everyone else

Some runners fear the possibility of injuries such as shin splints, twisted ankle, etc. But imagine running a 5k with these injuries- along with cerebral palsy. Renowned sports writer Rick Reilly captures the moment Hanna High junior Ben Comen, who’s body is wrecked by cerebral palsy, crosses the finish line of his cross country race in the piece ”Worth the Wait”, written in 2003. Flagged by his teammates opponents, and even the girl’s team Ben tumbles in a last ditch effort across the line to the screams of the crowd. It’s near impossible to imagine what it’s like to not control your body for such a long distance, enduring the adversity along the way, but Reilly pushes the reader to run alongside Ben throughout the story. He paints an image

Many people these days take their health and body for granted. Imagine losing the ability to walk suddenly due to an accident or a disease. This is exactly what had happened to Nancy Mairs, author of the essay “On Being a Cripple.” She herself had lost her ability to walk normally when she was diagnosed with multiple sclerosis or MS, a chronic disease that attacks the central nervous system. Her essay talks about her life and dealing with MS. The purpose of the essay is to show how being crippled affects your life and how to stay positive and deal with it.

When undermined by an incurable disease, it’s difficult to think positively. Especially with multiple sclerosis, where life adjustments - including changes to communication, daily routines, even basic bodily functions - are necessary, it’s likely to approach situations hopelessly. However, essayist Nancy Mairs provides her own detailed anecdote on accepting these lifelong impairments. In her essay, “On Being a Cripple,” Mairs develops her attitude toward her condition through multiple accounts of asyndetons, figurative language, and her personal experience.

In the essay “On Being a Cripple” by Nancy Mairs reflects her life as a “cripple” because of MS, and her recognition of it. Mairs purpose is to inform individuals on her perspective on being a cripple. She describes how she views herself and how others look at her. Mairs use of word choice, tone, and examples of her life experience provides a better understanding to the goal of this essay.

The writer of “On Being a Cripple” by Nancy Mairs, describes her life as difficult, but not entirely worth the cure. The writer struggles with multiple sclerosis, a chronic degenerative disease of the central nervous system, in which had weakened the left side of her body into wearing a cane. She experiences society pressures, false interactions, and many hard situations of having a body that hardly works. However, she carefully names herself as a “cripple”, and remains proud with being just that. The author never had any control over receiving this disease, however she had enough control in order to keep living with it.

Jennifer Bricker never saw her disability as a limitation thanks to her adoptive family (Zagoriski, 2014). Although Jennifer was born without legs, her heart was always set on gymnastics. Her positive spirit lead to her domination in competitions and later, the Junior Olympics. Jennifer created motivation to persevere, used persistence to overcome being legless, and illuminated the world by inspiring people to pave their own road of destiny.

I was talking about what it’s like to be a rider. Get it?” Linda 15” So all and all at first she didn’t really want to talk about her disability but know she has come out of her shell and isn’t afraid to talk about it. This is how she overcame her obstacles and coped with

Brooke Ellis, despite having been in this accident and becoming a quadriplegic, did not slow down one bit with her life. She was proactive, not reactive, to her situation. She still held on to her dreams even though some may be impossible with her condition. When in rehabilitation,

Britt was born in New Jersey, she was a shy person who liked the outdoors. She did many activities outside like hiking, biking, and skiing when she had her vision. Then one night she lost nearly all of her vision in her right eye, and lost most of the peripheral vision in her left eye over the next 9 months. Over the years the vision in her left eye continued to diminish. Now she is completely blind, but that didn’t stop her from skiing. At first it was hard for her to adjust. For a while it was trial and error till she found a system that works. She goes down the hill by following the sound of her husband’s voice and board. She said that skiing is more fun now because the stress of skiing is now off of her shoulders. Skiing is not the only thing that she does. She is also an oceanographer.

MacLaren quickly recovered and began his journey to change disabled people’s life. He became and active athlete again by competing in triathlons (ESPY). He proved that an athlete could be disabled and still win medals. MacLaren would soon face another tragedy while he was doing the one