Interview Finding Her Way Analysis

This paper will inform the parents, educators, and American society of the benefits of therapeutic horseback riding for people who have cognitive challenges or loss of limbs and other functions. Therapy can happen on the horse as well as off, depending on the condition of the rider. Not all therapy has to be done on a horse. It can be done on the ground as well, by padding the horse, brushing the horse, leading the horse. Knowing you can conquer being around and taking care of a big horse gives those with challenges a sense of satisfaction and self confidence. Therapeutic horseback riding is wonderful for young people as well as older people with disabilities. Even if they cannot sit up straight, therapy can make it so that any individual can

On the other hand, Amy Tan brings up similar hardships, however, the way she explains them may imply that they are not at all “hardships” in her opinion. She grew up the daughter of Chinese immigrants. To other people, they hear her mother speak English and automatically consider it “broken” or “fractured” English. Tan expresses that she does not consider it broken at all. She begins to explain that when she is speaking to her mother, being the successful writer she

The amount of people who live with disabilities is a controversial number. Depending on what law and diagnostic tools used, a person may have a visible disability, or one that may lie beneath the surface of his or her appearance. Some people believe that the term “disability” is merely a label use to hold back, or prescribe helplessness. Meanwhile, individuals who have been properly diagnosed with disabilities struggle to maintain respect and acceptance every day. In plain language, there is a lot of misunderstanding between people with disabilities and those without. It is firstly important to get everyone on the same page regarding the definition of disability.

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

The moment she got trampled under the stomps and shoves of others, one could identify what she’d been feeling like previously - a witness to her own inconvenience. This incident not only exemplifies but also symbolizes the burden she feels having been born handicapped, unable to provide assistance or gain to the world. These feelings Adahs has for her life are later rebutted by her longstanding dreams of attending medical school and improving science. By achieving her academic potential, she finally recognized herself as an important asset to the world- no longer being seen as handicapped, physically or mentally.

The book challenges perspectives by daring the reader to empathize with a minority group and try to see from a point of view less commonly discussed

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.

“On Being a Cripple” is placed under the genre of autobiography because it focuses on a significant personal experience in Mairs’ past and draws out the meaning as she tells her story and reflects on her experiences. The key factors of an autobiographical essay include dramatic events or episodes, vivid details and narration, and an interweaving of narration with reflection on and interpretation of the essayist’s experiences (Norton xxvii). This essay focuses on Mairs’ experiences and personal struggles with multiple sclerosis.

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.

When you see a disabled person, what goes through your mind? I tend to not pay too much attention or put too much thought into it, but I really should. Being disabled is hard and changes people's lives dramatically. We can see how Nancy Mairs life has changed in her essay “On Being a Cripple”, and in Matthew Soyster’s essay “Living Under Circe’s Spell”. Both authors are victims of a disease called multiple sclerosis, which damages nerve fibers and interrupts the nerves’ signals.

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.

Michael’s Story: “I get into so much trouble just by walking”: Narrative Knowing and Life at the Intersections of Learning Disability, Race, and Class

Disabilities within the characters of “The Life You Save May be Your Own” by Flanner O’Connor

Laura has let her disability affect her entire life. Williams uses these incidents to show what happens when people allow their disabilities or shortcomings to plague their lives. When a person is handicap, he or she can still live his or her life to the fullest. They should grip this deficiency and