The subject of ‘disability’ has always become an awkward and unsure one. The trouble, perhaps, is caused primarily by a sense of discomfort regarding the ‘proper’ emotional response towards the ‘disabled’ people. Generally, it is a confused feeling of compassion, anxiety, apprehension, pity, annoyance, detachment, self-complacency and even guilt. Moreover, the borderline between ‘ability’ and disability remains vulnerable and indefinite, as nobody can assure that the ‘able-bodied’ people will remain so till their death. It creates another uncomfortable realisation about the impermanence of body. In fact, the attitude to disability is a cultural construct. The emotional reaction to it is closely associated with the accepted standard of physical …show more content…
Excessive emotional reaction to ‘disabled’ ones often tended to become melodramatic. It was, in turn, subject to manipulations. This is reflected in Henry Mayhew’s encyclopaedic London Labour and the London Poor (1861-2). Andrew Halliday presents here a vivid picture of the numerous kinds of physical disability that could be found frequently on the streets of the city in the mid-nineteenth century. It reveals that many of them were imposters. A considerable number of ‘beggars’ “exhibited” their impaired bodies as their sources of income (431). Those who used their ‘disability’ and ‘deformity’ seemed to dwell on a different sphere of life and …show more content…
Referring to Catherine Peter’s biography of Wilkie Collins, Kate Flint suggests that Collins’s interest in “obstacles to full physical functioning”, may be seen partly as a result of his own eyesight-related problems (he suffered from chronic ‘eye gout’ and consulted the ophthalmic surgeon George Critchett about this) (Flint 153). Collins’s reliance on melodramatic tradition has also been suggested as a reason for his interest in physical disability. On the other hand, Flint refers to a broader nineteenth-century concern “with the operation of the senses” in this respect (Flint 154). In her observation, this concern was demonstrated in various fields such as literature and science of the period. The popular literary texts often showed a “theological bias”, suggesting that some spiritual consolation could follow physical deprivation. Contemporary scientific works that studied and made various developments in the fields of physiology and psychology paid attention to “variation and aberration within human perceptual systems”. There was an attempt to make generalisations about the ‘normal’ functioning of the senses (154). This attitude was duly mirrored in the representation of ‘disabled’ characters in the contemporary English novels. For example, we may mention the diminutive persons of The Marchioness in Dickens’s The Old
And if “Had anyone been there with her, she’d have been still and faint and hot with chagrin, (Mairs 259).” Instead of pitying herself, Mairs is able joke about her hardships in her day-to-day life despite having physical incapabilities. She then continues with a steady, yet uplifting tone as she explains the reasoning behind why she labels herself as a “cripple”, stating that it is a “clean word, straightforward, and precise, (Mairs 260).” She believes that words like “disabled” or “handicapped” are words that are “moving [her] away from her condition, to be widening the gap between word and reality, (Mairs 260).” By using these euphemisms for her condition, people tend to view her as something she isn 't.
Society perceives disable people as unable of doing the daily duty’s that a normal person could do. But in fact, they are wrong. Nancy Mairs describes how she was able to teach writing courses and teach medical students on how to give neurological examinations, making reader able to see that although , she was a “cripple” , she was able to perform some of the work of a professional person in the work- field. According to Mairs’essay “with only one usable hand, I have to select my clothing with care not so much for style as for ease of ingress and egress, and even so, dressing can be laborious”(3). Making it almost impossible for Mairs to dress up, she was to put on the necessary clothes that she needed to be covered by a piece of fabric clothing.
In Eli Clare’s essay titled “The Mountain”, she writes about her disability and how societal attitudes about it affects her experience of her own body.
In American society, if American’s do not look the same as society’s ideal image, then they are not considered normal. Those non normal American’s are treated as if they have a plague and are left on the outside always looking in. The people who have something that sets them apart from the norm, such as a disability, should not be treated differently than the people who are society’s version of normal. In “Disability” by Nancy Mairs, the problem of judging a book by its cover discusses individual examples relating to people who have a disability. Mairs’ essay discusses having a disability in a world where disability is ignored, especially by the media.
Today in the present, we as well have handicaps in our society, but as mentioned before, they are ‘hidden in plain sight’. An example
Murphy lacks mobility and sensation in his lower body other than the feeling of occasional muscle spasms, and has limited movement in his upper body below the neck including his arms. Murphy writes the story as it recounts events throughout his entire life, from childhood onwards. He was sixty-two when he wrote the novel. The story provides Murphy’s anthropological commentary on the life of a person with a disability and how society views and treats people with disabilities (Murphy, 1990). Murphy’s performance patterns both support and inhibit his occupational engagement.
In the essay, “On Being a Cripple,” Nancy Mairs uses humorous diction and a positive tone to educate people about life as a cripple and struggles of people with disabilities. She does this to show how hard it is to be disabled and how it differs from the life of someone without a disability. She talks about the struggles and the fears that disabled people must deal with on a daily basis. Mairs use of rhetoric creates a strong sense of connection and understanding for the reader. Nancy Mairs is successful in using detailed imagery, diction, and tone to educate her readers about the difficulties of living with a disability.
Mairs states, “People-crippled or not-wince at the word “cripple”... Perhaps I want them to wince” (245). She does not believe in just trying to sympathize what she has, or to even fool anyone. Her choice of the word “cripple” is a strategy she uses to confront the social issues regarding her
When people hear handicap they think not able to care for themselves. Nancy wants to be known as a tough individual able to take care of herself. The reader can feel the agony of what Nancy is feeling. The tone of this passage is determination and agony. Nancy feels that cripple is more stronger word than “handicap” or ‘disabled.”
Individuals, who suffer from any type of disabilities, sadly live a different life due the societal stigma attached to it. The film When Billy Broke His Head and the reading Deaf Matters Compulsory Hearing and Ability Trouble both illustrate the hardships and struggles disabled individuals go through as a result of stereotypical misconceptions created by the media and the larger society. Firstly, exemplified in the media through a portrayal of disheartened characteristics like constant anger and bitterness about life, a misconception of an unapproachable individual starts to become produced. Through a continuous loop of negative illustrations of disability, an unawareness and lack of knowledge about certain disabilities, a stigma of this unfamiliar
Within Sheila Black’s Passing on my Disability is the opinion that a disadvantage, like having a disability, does not mean the withdrawal of a person from what would be considered an ordinary life. In the opening of Black’s essay, the author mainly focuses on laying down the foundational knowledge required to understand her story, including her family and her condition, X-linked hypophosphatemia (XLH) — a form of dwarfism — that debilitated herself and two of her children. During the most of the middle of her essay, Black proceeded to further elaborating on her and her children’s life. The author mentions many of their difficulties and pains, such as when Black writes on the difficulty of seeing her “loved one [with] that psychic pain” everyday
n Nancy Mairs essay, “Disability”, she illustrates the lack of representation of people with disabilities in the media. While disability plays a major role in Mairs’ life, she points out the various ways her everyday life is ordinary and even mundane. Despite the normalcy of the lives of citizens with disabilities Mairs argues the media’s effacement of this population, is fear driven. She claims, “To depict disabled people in the ordinary activities of daily life is to admit that there is something ordinary about the disability itself, that it may enter anybody’s life” (Mairs 14). Able bodied people worry about the prospect of eventually becoming physically impaired.
For anybody, being employed can have a crucial impact on their lives. It also has great importance on our social and material well being. Income, self-esteem, identity and sense of independence are just a number of benefits that people can gain from being an active and useful member of the workforce. Yet from a historical perspective, many disabled people have been denied such benefits because of their exclusion from mainstream social and societal activities such as worthwhile employment in particular. Interestingly, disable workers have in the past found themselves welcomed and encouraged into employment during time of shortage of able bodied workers during times of war (Barnes, Mercer & Shakespeare 1999, p.22).
In this report I will discuss both the Social and Medical Models, define their pros and cons and give a short reflection on my own opinion of the two models in everyday use today. Both the medical and the social models of disability describe how they see disability and how they feel disabilities and those suffering should be treated. Both models have very different views on the causes of, how disabilities should be taken care of and by whom and both have their strengths and weaknesses when it comes to caring for those with disabilities. Medical Model
And a disabled person’s ambition is like all other human beings, the looks of pity and compassion negatively affect that ambition. People should embrace the disabled person and give them a helping hand, and they should have laws, which defend their rights, which should be respected. However, most societies do not have laws that ensure an equal life for the disabled population. It is a shame that the rights of the disabled people has turned many times to mere slogans.