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In this paper I will be writing about what I have learned from researching Individuals with physical disabilities. I will be writing about the interpersonal relationships they may have with attention more on dating, romance, and sex. Whether it is our friends, relatives or siblings, we all happen to know at least one person in our lives who happens to have physical disability. The fact that they are disabled does not mean that they cease to live life like the rest of their able bodied counterparts. I have learned this from having a sister who is physically disabled. So this topic is yes, personal and important to me. As it should be to everyone who comes in contact with someone with a physical disability. A physical disability is a limitation …show more content…
Yes, they can. However, for some people, their disability can impact sexual function such as a loss or change in sensation, difficulty controlling the muscles, and some men may not be able achieve or maintain an erection. People with spinal cord injuries have reported experiencing great pleasure from stimulation in areas like the arms, earlobe, neck, cheek, and nipple, so much so that it can also lead to orgasms. A lot of sexual pleasure is about what happens in the brain too. There are all sorts of ways to go about this, whether it’s through fantasies, relaxation, meditation or breathing techniques. It’s all just a matter of working out personal turn-ons and turn-offs and the best way to do this is with a loving partner that they trust. There are many ways that people with physical disabilities can find help with their sex lives. Many individuals find a certified sex therapist. Sex therapy can help with a variety of issues including erectile dysfunction, low libido, and other sexual problems. There is also the option to visit a clinical psychologist who will help with understanding, preventing, and relieving psychologically based distress or dysfunction and to promote subjective well-being and personal
She told her readers that she has a muscle-wasting disease and she could only move three fingers on her right hand. She wrote that the reactions she got from most people were “Decidedly negative” (Johnson p.98) She wrote that she would hear thing such as “I admire you for being out; most people would give up.” And “You don’t let the pain hold you back do you?” (Johnson p.98) There is often talk about how popular culture teaches people to both see and not see the people with disabilities. Comments such as these are an example of such blindness. When a child sees a disabled person a parent’s first reaction would be to tell them not to stare. We teach children that it is impolite to be curious about people who live life differently than others. We carry the “its-not-polite-to-stare” idea into adult hood therefore when we come across a disabled we try not to make eye contact not as if we are being rude but because we are taught that it would offend them. All curiosity and attempts to understand are shut down at a young age for fear of offending someone. Therefore, any attempt to encourage is met with a deep misunderstanding of how the life of someone with disabilities truly works. Just because a person has a disability does not mean they are incapable of enjoying
Most people feel relatively uncomfortable when they meet someone with an obvious physical disability. Usually, the disability seems to stand out in ones mind so much that they often forget the person is still a person. In turn, their discomfort is likely to betray their actions, making the other person uncomfortable too. People with disabilities have goals, dreams, wants and desires similar to people without disabilities. Andre Dubus points out very clearly in his article, "Why the Able-bodied Still Don't Get It," how people's attitudes toward "cripples" effect them. It's is evident that although our society has come a long way with excepting those with physical disabilities, people do not understand that those with physical disabilities are as much human as the next person
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.
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
As human beings, we like to make sure never to offend or judge anyone. We even have sayings like “never judge a book by its cover”. A metaphor that is often said whenever trying not to judge someone based on their outward appearance; however, it is not often that people practice what they preach. We judge people based on external factors within seconds. Even though we know what people see on the outside is not a defining factor or who we are as people. Nancy Mairs, author of On Being a Cripple, has to live through this every day. She knows this truth very well, and lives proudly with the fact that as she is disabled. Mairs is admirable for choosing to call herself a “cripple” and not be ashamed of it. Though the word is derogatory and a word that is avoided by society, Mairs identifies herself as a cripple because that is what she is. In explaining her disability, she says, “I haven’t always been crippled, ... to be whole of limb is ... infinitely more pleasant and useful. and if that knowledge leaves me open to bitterness … the physical soundness I once enjoyed is well worth the occasional stab of regret” (Mairs 186). What really
Popular culture does not showcase the intimate lives of people with disabilities because society does not acknowledge that people with disabilities can participate in sexual activities. Nussbaum explores this common misconception in her novel, through the characters of Yessenia Lopez.and Joanne Madsen.Yessenia seems more comfortable with her sexauality than most teenagers with disabilities.She
Society must realize the “collective obligation and responsibility to treat people with disabilities not as recipients of charity and goodwill, not as objects of compassion, but as the primary subjects of justice” (Kuick 292). Every individual deserves the opportunity to be sexually active, regardless of his or her physical or mental abilities.
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
Although the reader is moved by Krents many stories and examples, the lack of objectivity in the essay leaves the reader with doubts. Krent’s theme - that if handicapped persons were viewed fairly their disability would be not be apparent- is one that the reader is aware of and wants to believe in. Yet, Krent’s own pessimistic tones overshadow the greater good. The reader is left with the unpalatable feeling that this essay may be nothing more than a very unconfident and dissatisfied man, attempting to pin his disappointments and failures on society, so that he may feel better about himself.
Tim Rose and his wife Natalie Rose have experienced many assumptions and stereotypical comments solely based on their appearances. Natalie is able-bodied, and Tim was born with cerebral palsy (Verstraten, 2014). The Roses have created the “Rose Centre for Love, Sex, and Disability” which aims to promote disability in a positive light, and educate disabled and able-bodied people around the topics of love, sex, and relationships (Verstraten, 2014). The chosen cultural artifact addresses the conversation of a romantic relationship between an able-bodied and a disabled person, and touches on the stigmatization surrounding this relationship. The cultural artifact is a Toronto Star news article titled “Surprise! Disabled People Have
Disability is defined as a long term condition that restricts an individual’s daily activities (Government of Western Australia Department of Communities, n.d.). A disability can be identified in numerous types which are physical, sensory neurological and psychiatric. Due to the assistance with appropriate aids and services, the restrictions experienced by individuals with a disability may be overcome. However, the ways society perceives disability may have a significant impact on individuals living with it and also families around them. Therefore, the aim of this essay is to reflect on the social construction of disability through examining the social model of disability and how it may impact on the lives of people living with disability.
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.
Societal views and conceptions on disability and disabled sexuality have undergone many changes throughout history. However, negative, misinformed, and neglectful views on the sexuality of the disabled have been prevalent for centuries and can be traced back to 1614 when the first diagnosis of "mental retardation" was recorded, with the cause of the mental condition being stated as an "overindulgence in sexual pleasure" (Wade, 12). These views continued into the first half of the 20th century, seeing some improvement starting in the 1940s, when eugenic sterilization was eradicated in the United States. During the second half of the 20th century, there was some progress made in the way people with disabilities were regarded and treated in society,
...eglected social issues in recent history (Barlow). People with disabilities often face societal barriers and disability evokes negative perceptions and discrimination in society. As a result of the stigma associated with disability, persons with disabilities are generally excluded from education, employment, and community life which deprives them of opportunities essential to their social development, health and well-being (Stefan). It is such barriers and discrimination that actually set people apart from society, in many cases making them a burden to the community. The ideas and concepts of equality and full participation for persons with disabilities have been developed very far on paper, but not in reality (Wallace). The government can make numerous laws against discrimination, but this does not change the way that people with disabilities are judged in society.
There can be many reasons for the issues. It can be a disease such as diabetes, substance abuse, medication, or even a psychological issue that causes the sexual dysfunction. I have had and experience with a man who had erectile dysfunction. (Impotency) Not only was his caused from diabetes, but also the fear of not being able to perform contributed to the issue. Women experience sexual dysfunction as well. Menopause can contribute to sexual dysfunction in women. Many women have to use lubrications because their body does not produce adequate lubrication for intercourse. The book states that people with spinal cord injuries can have sex lives. I was actually surprised by this. I could not imagine desiring to be sexually active if I were in a wheelchair. I think I would feel useless if that were the case and would have little desire to do much of anything. However, I have never been faced with that so I am unsure as to how I would