Story Of Edgar Sawtelle By David Wroblewski

Furthermore, a personal experience I encountered was when I took a high school class with a girl who was also deaf. Even though she was not exactly like Ildefonso, she opened my eyes to a different world that many people do not understand and do not care to understand. On another note, some of the reading voices I had influenced the way I read at times. For example, sometimes I would read a particular line, such as “I thought Charlie—the retarded man in Flowers for Algernon, and the experiment to make him intelligent (p.58),” and refer back to the time when I read that book and start thinking about how cool it was that Susan mentioned this. Then I would create an elaborative thought of what other things Susan and I may have in common with other related or non-related experiences. Additionally, when I read, “By now he should have learned enough language to answer some of my old and new questions in detail(p.142),” I had suddenly thought of the time back when I was in kindergarten writing out my ABC’s. Throughout the whole paragraph of “reading,” I was just in one deep thought about what it would be like not being able to match words with thoughts. These examples were both illustrations of distracting voices.

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

Tracy’s pain was exaggerated in the sense that her handicap was a “terminal illness” (Malhotra). Crown, Canada’s government, tried to convince the jury that Tracy had “enjoyed outings… She also responded to visits by her family… her life had value and quality” (News). There are other parents who have children with much severe disabilities yet do not come to the conclusion of ending their child’s life.

These views change possibly because a disabled person, whether a friend or family member, may be acquainted with them. Treating another equally removes these preconcieved beliefs. In the story, the audience enters the narrator's mind and sees the narrator's bias; furthermore, the narrator explains that he has "never met, or personally known, anyone who was blind" (5). The mind is powerful enough to convince people that they are seeing reality; however, empathizing with the disabled, whether through drawing a picture or conversing, reveals the flaws in people's

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.

Jon Owens was born on March 1, 1960. Jon’s parents feared of having a child with mental retardation. Jon family members are mom is a psychotherapist and dad is a psychiatrist. Jon had two sisters Jennifer and Jennice and a brother Charlton. Jennifer is a filmmaker. Jennifer says Jon is a spiritual teacher. Jennice is a keynote speaker. Charlton is a lawyer and doctor. When Jon was born, a pedestrian told his parents he would never reach age 5. Jon’s parents spoke with a fellow friend and doctor who had brother with Downs’s syndrome. The family friend expressed the grief of putting brother in an institution and how it ruined his family lives. Jon’s parents thought it would best to put him in nursing home. Jon was in a crib all his life. Jon lived in a nursing home for 6 ½ years until his caregiver died. Jon’s parents had received a call to make decisions on Jon’s care. Jon was diagnosed with having Down’s syndrome. Jon was more than a little slow, but mentally retarded. Jon had limited intellectual and physical abilities.

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.

The time the story is set in is in the 1950's, this can be inferred by the use of terms such as jukebox and milkbar, as well as the slang ‘garn, you're keen on that dago.'

“Reading gives us someplace to go when we have to stay where we are,” (Cooley). Throughout our lives, reading has impacted us in many ways. Often times books give people different perspectives on their lives. People with high stress levels often find comfort in reading books to take their mind off of their concerns. Sometimes, people just need to take a step back from their lives and relax for a while; therefore, reading is a great tool. In fact, all kinds of books have also helped me become a better writer. There are many different books that have impacted me over the years.

Mark Drolsbaugh’s autobiography, Deaf Again goes through his life journey as a deaf individual who tries to find his Deaf identity in the hearing world. Mark was born as a hearing person, but as he got older he gradually started to lose his hearing which made it difficult for him to fit in as “normal child.” When Mark was in kindergarten, he started to feel lost with his classmates and heard less and less. After this incident, his grandfather took him to numerous doctors to find a solution for his hearing loss, but there wasn’t any resolution. Despite the fact having deaf parents who knew sign language, Mark was never encouraged by his parents nor grandparents to communicate in sign language, they were told by doctors that signing would interfere

However, his argument does not address the children's well being, but solely discusses the parent's’ view of their child's disability. This therefore does not justify his argument that disabled people do infact have a lesser level of wellbeing. Singer sympathy towards parents of disabled children distracts from the imperative argument which is the wellbeing of the disabled child (individual), and if he/she has the same ability to attain a somewhat ‘normal’ level of

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

suffers horribly so that the rest can be happy” (Brooks). The child’s pain and loneliness is a

Lucy Grealy tells a story about not fitting in, unbearable pain that takes up residence in one’s head as loneliness and confusion, questioning what things mean, being scared and lost in your family, enduring intense physical pain, and most importantly, figuring out who you are. Lucy had no idea she might die, even though the survival rate for Ewing’s sarcoma was only five percent. She does not present her parents as overly afraid for her life, either. Her autobiography is not a story about the fear of death, but about such courage and anguish. Lucy shows how she falls under the spell of her disability, allowing it to control her life and dictate her future to a greater extent than it would otherwise. Having a disability means that

An individual with intellectual disabilities can face many barriers in not only their academic life, but also their social life. Peter, has faced barriers to his successful inclusion in the classroom. One of the barriers the video mentions is teachers displaying unwillingness to including Peter in their classroom simply because teachers do not accept him or his disability. I believe prejudice is a barrier many people with intellectual disabilities are forced to face at a given point in their lives. I think the prejudice stems from fear and misunderstanding of people who are physically or mentally different. In chapter nine of this week’s readings, it highlights on the importance of individual relationships are between the teacher and the student with a disability. Focusing on a student’s strengths rather than there IQ or weaknesses is essential to their success. “Some teachers focus on her IQ, but that’s not a useful fact. Everything depends on the relationship Rachel and I have with educators, on their skills, and on Rachel’s attitude, behavior, and self-determination.” (Turnbull. p. 187). Another barrier Peter faces is the desperate struggle of wanting his independence, yet still needing outside assistance for things. The loneliness and the inability to properly communicate his emotions are one of the biggest mental barriers Peter has faced. Peter overcame and managed these barriers through