Chris Gabbard A Life Beyond Reason Analysis

Some family have stereotypical ideas about disabled, but for Amy Purdy and her family that motivate them to live their lives beyond their limits. Although, she lost some parts of her body. For example, she lost both her legs below the knees, the spleen, kidneys. Unfortunately, she became unable to hear in her left ear. Another person who born with disability, Maysoon Zayid which is cerebral palsy. However, she did not give up for this so she worked hard and persevere to get a scholarship which was from Arizona State University. From Amy Purdy and Maysoon Zayid, we learn that facing problems forces us to get creative, and we should be optimistic when we want to change a critical situation.

57) Disabled families often face the effects of stereotypes of disability through government systems where disabled families are often portrayed to be dependent, incapable, and unreasonable. This reality often excludes disabled families from the decisions that affect their lives, and their needs/desires are put aside to favor protecting normalcy. Facilitating interdependence among disabled families and the greater society could bring new light to the experiences of disabled families. Many disabled families fear that they will be separated if deemed “too disabled” to care for one-another, which often prevents them from “coming-out” or asking for help (Wilde & Hoskinson-Clark, 2014, p. 57. Opening communication channels, and fielding trust and creating supportive foundations by directly considering what individual disabled families and want can largely improve life for those with disabilities and impact their perception and acceptance by the larger society. When disabled people feel as though they are understood, protected, and considered in the decisions that impact their lives a sense of independence develops, and the misrepresentation they experience can be largely reduced to allow individual autonomy to

In the video “Inclusion, belonging, and the disability revolution” (TEDTalks, 2014), speaker Jennie Fenton opens with describing situations where people with disabilities are segregated and excluded from their communities, sent to live together away from society, or even treated as lesser humans. She then proceeds to introduce her family, including her six-year-old daughter that was diagnosed with cerebral palsy. Jennie admits to previously having negative or frightened thoughts about having a child with a disability, but with her “seven realizations,” she learned that her daughter was merely on a different path than others, but that no one should ever feel broken or not a whole person (TEDTalks, 2014). After she explains that there are roughly one billion people with a disability throughout the world, Jennie states that she believes in possibility over disability. If a person’s

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

Unspeakable Conversations by Harriet McBryde Johnson is an article about her experience visiting Princeton University to exchange views and challenge Peter Singer, a professor who strongly believes that all disabled people, like herself, are “better off” not been born at all. The article provides an insight into Johnson’s life as a disabled person. She takes the readers on a journey that explores both sides of her own and Singer’s contrasting beliefs. She protests the prevalent stigma and prejudice of disabled people and gives voice to this marginalized community. Johnson challenges stereotypes of disability, uses her a personal experience to better understand the world and help others, and attempts to directly address oppression by arguing against Professor Singer’s theory and assemble a group of diverse and like-minded people for social change.

Disability is a topic viewed differently by each set of eyes. To truly understand a disability, one must live through it or frequently view the lives of another, struggling with an infirmity. Living with a disability may be hard, but it does not mean it is not worth living. Nancy Mairs, author of the essay “On Being a Cripple,” has written about her views and experiences, explaining to the public the truth behind being a “cripple,” and proving that disease does not control you. Explained in the paper, able-bodied people make assumptions to how low quality life must be, living with a disease and that these individuals are constantly unhappy however

Humans are social creatures. We identify ourselves through our community, loved ones, and those who genuinely appreciate our presence. Our identity defines our personality traits, highlight social roles. Those with disabilities are often confused about their identity because they are misunderstood and stigmatized. Through the use of literature, one can empathize better with other people especially those who are misunderstood by society. Disabled people are more likely to be neglected and subjected to prejudice or discrimination. In “Delusion of Grandeur”, Terry Ann Thaxton, talks about the struggle between Adam and his mother because of his disability. Adam struggles to cope with his environment and finds himself isolated and misunderstood. Families ultimately suffer but through their experience, they can learn some amazing lessons.

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.

Those with disabilities have to accept their lives as being deprived of some joyful instances that may never happen. Individuals with handicaps may not be able to be active with their (or other’s) children, dream jobs may not be within grasp, memories may not be accessible while other’s take them for granted and shun those who desire that which they’ve already acquired (“People With Disabilities”). Provided, life is hard with a disability but additionally, those with handicaps must suffer isolation which is unfavorable in multiple ways. With isolation the person has no help, no support, no companionship, and feel ultimately rejected shutting them down in a social manner (“People With Disabilities”).

A lot of non-disabled people go through life carelessly, thinking, “What does it matter if I just sit back and do nothing?” Or think that they can do anything they want and everything will still be fine, just taking life for granted. There are people out in the world like Peg a girl from the narrative “The Incomplete Quad”, who can't even go through everyday life by themselves. The narrative “The Incomplete Quad” goes into the lives of people like Peg and Dale and shows us how much they actually go through or rather how much they can't. The story's main focus is on the lives of Peg and a guy named David, C average slacker who thinks he can get through life Doing nothing. He goes to college at Kent state and is roomed with a guy named Dale but when Dale moves back home David’s roomed with Peg. The story follows their lives and the journey of David coming to realize that he needs to change his ways because there are people out in the world like Dale and Peg who would kill to be in his position and be able to live life with half the freedoms he has. In “The Incomplete Quad”, David Sedaris shows that non-disabled people take life for granted by using characterization, humorous diction and the climax and resolution of the story

In the essay “On Being a Cripple”, Nancy Mairs shows us a class of two subcultures: being a parent and being disabled. Looking at the intersection between these culture and identities will show us important facets of disability that all people should understand. Throughout the essay Mairs explains the effects Multiple sclerosis and how it negatively and positively affects her life and the lives of her gracious family.

Stella Young has lived with a disability all of her life, but has never let that stand in her way. While speaking at a TED conference in 2014 Young wanted to address an issue that most individuals overlook. This issue is about people with disabilities and the struggle they face every day to feel equal and part of a social norm. Stella speaks from experience and tries to make her audience see a new perspective of how individuals look at others with disabilities. Stella makes it clear that most individuals see people with disabilities as an inspiration which is widely propagated. In order for her audience to understand this view she shows a series of images to appeal both to logos and pathos. Stella wanted to show that we view these images logically

“Steve, my oldest son, was born with cerebral palsy, which in his case meant both mental retardation and muscular spasticity. Although he has a tough time doing things that others find easy, he can manage most everyday things. When his mother reprimands him for bad manners, such as not using a knife to cut his food, he gets angry and says, “I can’t help it. I was born that way.” Whenever he says that, my heart goes out to him.

The book called A Very Special Critter by Gina and Mercer Mayer is a book about a new kid named Alex coming to class who is in a wheelchair. One kid in the class was afraid because he had never seen someone in a wheelchair before. Alex came into class the next day, and everyone thought his wheelchair was super cool. Alex made a lot of friends. The book explains that no matter what disability a child has that there will always be someone there to support him/her. A child in their wheelchair may feel lonely and get down on themselves. Perhaps because they feel out of place, and feel as if they are incapable of what all their friends can do. However, that is not true. In today’s society, there are many sports and activities available for kids who have a disability (Mayer, 1992).

Peter Singer, claims that “people with very severe disabilities are likely to live lives that are not as good” this blanket statement has raised a lot of questions, whereby, Singer defends his argument by claiming that people with disabilities do not have the same prospects as those born without disabilities. Singer’s claim is based on his assumption that disabled people are not able to achieve a decent level of wellbeing. He argues that people innately believe that disabled individuals are not capable of achieving a normal level of wellbeing due to, his idea, that mothers would not knowingly harm (disable) their children.