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Disability in modern society
Disability in modern society
Perspectives of disability
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My story began in February 2010, a fateful day that has since changed the meaning of a “disability” for me. My parents had been involved in a severe car accident that left them both partially disabled. Hearing the doorbell ring at four in the morning, only to see my grandfather brought upon such great shock. I am grateful every single day that they are still alive and with us children, and that they did not suffer more than they did.
After that day, things became increasingly difficult. My father’s leg had been injured in such a way that he could not stand for a period longer than ten minutes. His leg would become red and swollen; the pain was always present. My mother had to endure worse. She underwent multiple surgeries on her abdomen and right arm. We could not see her for the next two weeks. The healing process was slow and excruciating, and there was no way my parents would be well enough to continue working. Thus, in order for us to survive, my parents applied for government assistance which has showed us mercy and compassion during this point of great need.
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No relatives lived near, and they were much too busy to take time off to help care for my parents while in their semi-paralyzed state. Taking care of three younger brothers was a hassle, and I was also responsible for caring for my parents. I took up the cooking, cleaning, homework helping. Almost everything my parents used to do. Thankfully, my father was still able to move if he was cautious, and thus, he was able to care for himself and my mother in regards to personal hygiene. School was within walking distance, and although we once received rides to school, that was now not within the realm of
What comes into one’s mind when they are asked to consider physical disabilities? Pity and embarrassment, or hope and encouragement? Perhaps a mix between the two contrasting emotions? The average, able-bodied person must have a different perspective than a handicapped person, on the quality of life of a physically disabled person. Nancy Mairs, Andre Dubus, and Harriet McBryde Johnson are three authors who shared their experiences as physically handicapped adults. Although the three authors wrote different pieces, all three essays demonstrate the frustrations, struggles, contemplations, and triumphs from a disabled person’s point of view and are aimed at a reader with no physical disability.
As mentioned previously, the chances of becoming disabled over one’s lifetime are high, yet disabled people remain stigmatized, ostracized, and often stared upon. Assistant Professor of English at Western Illinois University, Mark Mossman shares his personal experience as a kidney transplant patient and single-leg amputee through a written narrative which he hopes will “constitute the groundwork through which disabled persons attempt to make themselves, to claim personhood or humanity” while simultaneously exploiting the “palpable tension that surrounds the visibly disabled body” (646). While he identifies the need for those with limitations to “make themselves” or “claim personhood or humanity,” Siebers describes their desires in greater detail. He suggests people with
Disability is a ‘complex issue’ (Alperstein, M., Atkins, S., Bately, K., Coetzee, D., Duncan, M., Ferguson, G., Geiger, M. Hewett, G., et al.., 2009: 239) which affects a large percentage of the world’s population. Due to it being complex, one can say that disability depends on one’s perspective (Alperstein et al., 2009: 239). In this essay, I will draw on Dylan Alcott’s disability and use his story to further explain the four models of disability being The Traditional Model, The Medical Model, The Social Model and The Integrated Model of Disability. Through this, I will reflect on my thoughts and feelings in response to Dylan’s story as well as to draw on this task and my new found knowledge of disability in aiding me to become
“Using Disability Studies Theory to Change Disability Services: A Case Study in Student Activism” outlines Syracuse University struggles with disability-related topics. Some of the university’s students formed a committee called Beyond Compliance Coordinating Committee to be the voice for the disabled students. The article follows their journey in struggles with implementing handicap-accessible areas and study material for a student that was blind (Cory, White, & Stuckey, 2010). This article reminds me of a close friend from my old neighborhood. He got into a really bad car accident that left him paralyzed from the waist down. After the accident some friends and I helped his parent modify their home to accommodate for his wheelchair. When tragic accidents like that help it really makes you put thing into perspective.
...r tended to her activities of daily living – feeding her, grooming her. However, her mother had no insight on her condition and how to help her take care of herself. I, personally took her to school and talked to teachers who advised to have her join a school for the disabled, she was falling behind in classes and it was affecting her mentally and emotionally. She was visually impaired and no one in the family knew until she took a vision test catered to her. She is now 22 years old, and it amazes me to see how she has flourished. A young girl who used to be glued to the television, watching cartoons and the likes, she is now on her iPad watching videos on YouTube, face-timing with friends and family. When our grandmother passed away a few years ago, she took it upon herself to console everyone. Had her growth been hindered, she wouldn’t be the person she is now.
This article was very interesting and there are a few key points that stand out. The author explained that it is important to be an advocate for your child by learning as much as you can about the disability that they have. Also, she mentioned that if a parent keeps on living in denial about the illness or disability, that this will never help the child or the parent. I also found it interesting when she spoke about support within the family as well as outside the family. Lastly, I thought it was important for her to mention the strain that a family with a disabled child will incur.
Thanks to Ed Roberts, Mary Switzer and Gini Laurie the 3 major players in the Independent Living and Civil Rights movement, people with disabilities now have access to public schools with an Individualized program, access to buildings, facilities, buses for transportation and are protected by law from discrimination. “Approximately 50 million people today lead independent, self-affirming lives who define themselves according to their personhood their ideas, beliefs, hopes and dreams above and beyond their disability” (A Brief History,
We had to adapt quickly and adjust our lifestyles in order to meet the responsibilities involved with being a caretaker. We had to teach ourselves about Medicaid, medicare and how we can find specialists for her condition. Upon gaining custody of my younger sister she was unable to move from the neck down due to a previous stroke. Therefore, it was our main objective to find her therapy and how we could pay for it. Fortunately, I stumbled across a nonprofit group known as HASCI, which helps people that have endured trauma to the head & spine. It was with their help my sister was able to partake in an intense physical therapy rehabilitation program. Moreover, they made a miracle happen because I wheeled her that first day of care and saw her leave those same heavy metal doors walking on a cane. It was also during that time my academic career suffered. As a result, I did withdraw from a few courses nevertheless, I was steadfast and maintained my focus for the courses that remained. Despite personal deviations my degree was prolonged in attaining yet I persevered through life's challenges to become a Biology graduate from
Helen Keller is probably the most universally recognized disabled person of the twentieth century. (Others such as Franklin Roosevelt were equally well-known, but Keller is remembered primarily for her accomplishments which are disability-related.) Those of us who have grown up in the last half of this century have only known Keller as a figure of veneration. We know her primarily through popularized versions of her life such as the play "The Miracle Worker," or through her autobiographical works such as The Story of My Life (Keller, 1961 [1902]) and The World I Live In (Keller, 1908). Most of us have come away with the image of a more-than-human person living with the blessed support of an equally superhuman mentor, Annie Sullivan Macy.
Life was different before my mom was diagnosed with a terminal cancer. I lived in a house with my mom and my two siblings. My parents were
In the essay “Disability,” Nancy Mairs discusses the lack of media attention for the disabled, writing: “To depict disabled people in the ordinary activities of life is to admit that there is something ordinary about disability itself, that it may enter anyone’s life.” An ordinary person has very little exposure to the disabled, and therefore can only draw conclusions from what is seen in the media. As soon as people can picture the disabled as regular people with a debilitating condition, they can begin to respect them and see to their needs without it seeming like an afterthought or a burden. As Mairs wrote: “The fact is that ours is the only minority you can join involuntarily, without warning, at any time.” Looking at the issue from this angle, it is easy to see that many disabled people were ordinary people prior to some sort of accident. Mairs develops this po...
“A History of Disability: From 1050 to the Present Day.” English Heritage. n.p., n.d. Web. 4
Fear is just a reason to try harder is a saying that you might think of . Well this type of fear is different . THere was a time in my life where i was just taken over by fear i was not happy at all i would not smile . I was really nervous about coming to middle school . I was nervous because there are so many new people here and the locks on lockers were a scary thing to me to make that transition .
It was a Friday night, and my friends, Ryann and Josh, and I were traveling to Nashville, Tennessee for a country music festival. We were in St. Louis when I remembered the traffic being really heavy, and Josh was our driver. Josh was very prohibitive with his driving, considering he had two other people in his car. Ryann suggested that he should get into his right lane, but he told her no. He said that we are prone to get into an accident if we switched lanes, so he was obstinate with his idea. All of a sudden I remember hitting the dash and being knocked out cold.
French, S. & Swain, J. 2008. Understanding Disability: A Guide for Health Professionals. Philadelphia: Churchilll Livingstone Elsevier: 4