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How media shape public perceptions
Describing the medical and social models of disability
The issue of discrimination against disabled people in our society
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An estimated one billion people are living with disabilities around the world, that is approximately 15 percent of all people on earth (United Nations, n.d.). Furthermore, in the United States, almost 57 million people, 19 percent, have some type of disability (United States Census Bureau, 2012). It is apparent that disabilities are prominent in life today, and unfortunately, the world views disability as individuals who are not abled. Eli Clare, author of "Stolen Bodies, Reclaimed Bodies: Disability and Queerness", acknowledges that there is a vast majority of people living with disabilities and in light of this, he advises the world to accept irrevocable differences. In this case, Clare argues that irrevocable differences are bodily differences …show more content…
that do not go away and that fact has a tendency to irritate people. Clare aims to enlighten society that while the world views disabilities as unnatural differences, they need to change their outlook to accept irrevocable differences in order to refigure the world. Eli Clare acknowledges that the world views disabilities in several ways.
Clare provides different paradigms of disability in order to demonstrate the wide variety of views concerning disabilities. He states that the paradigms of disability "all turn disability into problems faced by individual people, locate those problems in our bodies, and define those bodies as wrong," (Clare, 2001, p. 360). The first paradigm model Clare explains is the medical model which defines disability as a disease or a condition that is treatable. Next, he explains that the charity model defines disability as a tragedy and the supercrip model defines disability as a tough challenge that individuals overcome; the supercrip model makes individuals with disabilities out to be superheroes. Lastly, Clare explains that the moral model defines disability as a weakness. In order to demonstrate the paradigms and how they overlap, Clare cleverly uses an array of popular examples. One significant example is Jerry Lewis' telethon. During this time, Jerry Lewis attempts to raise money in order to find a cure for a condition. Overall, his Labor Day telethon raises money to end a disability by finding a cure for the broken bodies. This telethon employs the medical model because it demonstrates disability as a condition that needs to be treated. In addition, the telethon employs the charity model because it shows disability as a misfortune. All four disability paradigms are known as the social model because they are the ideas that society has about certain bodies. When society creates these ideas about disabilities, they create unnatural
differences. Countless people around the world view disabilities as unnatural differences. From this viewpoint, disabilities are seen as something that is not natural in the world surrounding them. In fact, people become irritated and discourteous with disabled individuals for a multitude of reasons. Time and again, people are aggravated with disabilities because they outpace social norms. It is because individuals understand themselves based on society, and social norms are formed, that disabilities do not fit within society. Gayle Salamon, author of "'The Place Where Life Hides Away': Merleau-Ponty, Fanon, and the Location of Bodily Being", refers to Merleau-Ponty when discussing unnatural differences because he discussed that that unnatural differences are "created rather than found," (Salamon, 2006, p. 99). Salamon explains that unnatural differences are socially constructed in which they are created by society, not found. She goes on to explain that "creation arises from an ongoing series of acts, of physical and psychic exchanges with the world that are sometimes unconscious and sometimes volitional," (Salamon, 2006, p. 101). Salamon is declaring that individuals consciously and unconsciously create unnatural differences. Unfortunately, many people around the world hold negative views towards disabilities because they believe it is an unnatural difference. Clare recognizes this setback, and while he acknowledges its prevalence, he advises society to accept irrevocable differences because they are necessary to life. In his piece, "Stolen Bodies, Reclaimed Bodies: Disability and Queerness", Clare introduces the term irrevocable difference. Irrevocable means that it cannot be changed or it is not capable of being altered. Different means that something or someone is not the similar. Tying both definitions together, irrevocable differences are meaningless variations that cannot be altered or change. Additionally, Clare reveals that irrevocable differences are necessary to life. He goes on to argue that irrevocable differences are necessary to life because it is a part of an individual's identity. Clare demonstrates this when he admits that, "so much of who I am is carried in my irrevocably different body," (Clare, 2001, p. 362). He embraces his irrevocably different body, and encourages others to do so as well. If irrevocable differences were to disappear, then the identity of individuals around the world would also disappear. Moreover, embracing irrevocable differences is difficult for many because countless people around the world do not accept irrevocable differences and the fact that they cannot be changed; rather, the world is going to great lengths to cure and fix bodies. Clare wants to rid the world of negative views towards irrevocable differences, and believes that it is beneficial to accept irrevocably different people. In order to demonstrate the negative effect society has on irrevocably different bodies, Clare discusses his body as a young child. Eli Clare realized at a young age that he was irrevocably different from those around him. To further explain the importance of irrevocable differences, he addresses his "disabled queer body" (Clare, 2001, p. 361). Today, Clare considers himself to be "white, disabled, and gender-queer", and accepts the fact that he is irrevocably different (Eli Clare, 2012). He had known from an early age that he was irrevocably different because his body would shake, he had a difficult time keeping his balance, had poor speech, and moved slow (Clare, 2001, p. 361). Rather than accept his irrevocable difference, people accepted Clare's disability as something that needs to be fixed, because he was broken and "unacceptably queer" (Clare, 2001, p. 361). Clare hopes to refigure the world and change the belief that disabilities are unnatural differences to the belief that irrevocable differences should be accepted. Irrevocably different bodies are seen as unique, whereas unnaturally different bodies are created and treated differently by people. Clare acknowledges that disabilities can be seen as an unnatural difference, but he promotes the idea of embracing disabilities as irrevocable differences instead of accepting it as an unnatural difference. In his piece, Clare writes "irrevocable differences could be a cause for celebration, but in this world it isn't," (Clare, 2001, p. 362). It is because people are forcing meaning onto the variations of people, and there is deviation from the norm, that there are differences. Clare encourages society to no longer think of disabilities as wrong or unnatural, and to accept or embrace them as irrevocable differences. In order to refigure the world, he warns the public that people must change what they believe about disabled bodies so that "they don't become storage sites, traps, for the very oppression we want to eradicate," (Clare, 2001, p. 363). In order to do so, people need to acknowledge their bodies, whether they are disabled or not. There is an alarming rate of individuals living with disabilities all around the world. Unfortunately, those individuals face the belief that they are unnaturally different, in which they are broken, wrong, and need to be fixed. Due to the fact that unnatural differences are socially constructed and implemented, Clare wants to shatter society's "belief that my body is wrong" in hopes of changing the world (Clare, 2001, p. 363). The author concedes that the belief that disabilities are an unnatural difference needs to vanish and in its place, the belief of accepting irrevocable differences should excel. The view that disabilities are an unnatural difference are harmful and results with "bodies stolen for good," (Clare, 2001, p. 363). Society needs to accept irrevocable differences, such as disabilities, rather than the belief that they are unnatural differences.
Eli Clare in Reading Against the Grain mentioned that the mainstream culture has a tendency to stereotype people into eroticizes culture such as thinking all African Americans males and Latino women are hyper-sexual, perceiving Asians as passive beings, and assuming that disabled individuals have no sexual desires. Somehow people regurgitate these stereotypes as if they’re empirical facts. Objectification usually reinforces or maintains the institutionalized power differences, which can deprive some groups such as the disabled from self-determination. The section of Pride and Exile brings to light how some members of the disabled community feels that they are denied of their personal autonomy. In Clares case, she explains how the MDA fundraisers
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
Gender has been broadly used within the humanities and social sciences as both a means to categories dissimilarities, and as a logical concept to give details differences. In both the humanities and social sciences. Disability studies has appeared partly as a result of challenges to give details gendered experience of disability and partly as a challenge to contemporary feminist theory on gender which fails to take description of disability. Disabled people have frequently been standing for as without gender, as asexual creatures, as freaks of nature, hideous, the ‘Other’ to the social norm. In this way it may be taking for granted that for disabled people gender has little bearing. However, the image of disability may be make physically powerful by gender - for women a sense of intensified passivity and helplessness, for men a dishonesties masculinity make by put into effected dependence. Moreover these images have real consequences in terms of
The memoir My Body Politic is an inspirational first person framework by Simi Linton. Her powerful stories give the reader a strong understanding on disability studies as well as the challenges Simi endured as she lived through a difficult time period for someone having a disability. When she became disabled in the 70’s, Simi’s life drastically changed. After spending months in the hospital and rehabilitation centers, Simi decided to take the opportunity to move to New York and attend college there. While living in Berkeley, she discovered that her neighborhood was more accommodating for people with wheelchairs, making it a welcoming space to live in. It was there where she discovered the political disability movement which inspired her to go back to university to get her bachelor’s degree in psychology.
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
The Moving Beyond Pity & Inspiration: Disability as a social Justice Issue by Eli Clare took place on April 16, 2014. Thinking about disability before this lecture I feel like I had a general idea of the things Eli spoke about. I attended a school were more than half of the students had a disability. The terms and stereotypes he mentioned I ha heard since sixth grade.
In” Disabling Imagery in the media “Barnes asserts,“Disabled people are rarely shown as integral and productive members of the community; as students, as teachers, as part of the work-force or as parents. “(11). Popular culture excludes women with disabilities because they are different. Through Joanne’s character, Nussbaum demonstrates how women with disabilities operate in their daily lives.Nussbaum description of Joanne’s daily routine shows that women with Nussbaum 's character Joanne also demonstrates how women with disabilities are not burdens on
Not only does Georgiana’s rhetoric depict how she subscribes to the opinion of “better off dead than disabled” but also shows how she falls victim to the medical model of disability. Georgiana refers to her imperfection as potentially “cureless” and demands he “remove” the flaw. Under the medical model, disability is seen as a pathology. If it is simply a pathology, disability not only has the potential to be cured but also must be cured. Additionally, the medical model’s goal of excising disability from society overlooks associated costs such as money and even
The two essays “On Being a Cripple” by Nancy Mairs and “A Plague of Tics” by David Sedaris are excellent pieces of work that share many similarities. This paper would reflect on these similarities particularly in terms of the author, message and the targeted audience. On an everyday basis, people view those with disabilities in a different light and make them conscious at every step. This may be done without a conscious realisation but then it is probably human nature to observe and notice things that deviate from the normal in a society. In a way people are conditioned to look negatively at those individuals who are different in the conventional
The Medical Model is one of the approaches used to understand people with disabilities, and is ‘concerned with the origin, degree, type of loss and the onset’ of a certain disability (Munoz-Baell &Ruiz, 2000; 54:40-44). This approach views a disability as something no human being wants and should be avoided at all costs if possible (Models-Deafness, 2005). The Medical Model aims to treat people with disabilities, but before treatment can take place they need to study the disabilities and conduct experiments. In some cases the tests and investigations conducted violate the subject’s (disabled person/people being studied) fundamental human rights (Chenoweth, 1995; 36). As stated in the Integrated National Disability Strategy (INDS) : Models of Disability (1997) the Medical Model is made up of establishments that cater to people with disabilities in terms of ‘providing treatment or alternatives’ to their impairment. Although they have good intentions (to assist the disabled) this models interventions result in disabled people being dependent on these institutions and the government.
Routledge: New York : New York, 2001. Shakespeare, T (2013) “The Social Model of Disability” in The Disability Studies Reader Ed Davis, L D. Routledge: New York.
Being disabled is just a single facet of their life, and they have the same capacity to be happy as anyone else. While these three authors have different reasons to write their essays, be it media unfairness, ignorance, or ethical disputes, they all share a basic principle: The disabled are not viewed by the public as “normal people,” and they are unfairly cast away from the public eye. The disabled have the same capacity to love, desire and hurt as any other human being, and deserve all of the rights and privileges that we can offer them. They should be able to enter the same buildings, have representation in the media, and certainly be allowed the right to live.
Every day in America, a woman loses a job to a man, a homosexual high school student suffers from harassment, and someone with a physical or mental disability is looked down upon. People with disabilities make up the world’s largest and most disadvantaged minority, with about 56.7 million people living with disabilities in the United States today (Barlow). In every region of the country, people with disabilities often live on the margins of society, deprived of some of life’s fundamental experiences. They have little hope of inclusion within education, getting a job, or having their own home (Cox). Everyone deserves a fair chance to succeed in life, but discrimination is limiting opportunities and treating people badly because of their disability.
Disability: Any person who has a mental or physical deterioration that initially limits one or more major everyday life activities. Millions of people all over the world, are faced with discrimination, the con of being unprotected by the law, and are not able to participate in the human rights everyone is meant to have. For hundreds of years, humans with disabilities are constantly referred to as different, retarded, or weird. They have been stripped of their basic human rights; born free and are equal in dignity and rights, have the right to life, shall not be a victim of torture or cruelty, right to own property, free in opinion and expression, freedom of taking part in government, right in general education, and right of employment opportunities. Once the 20th century