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How media influences socialization
Thesis for multiple sclerosis research paper
Thesis for multiple sclerosis research paper
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The Times Colonist report written by Katie Derosa on November 8, 2013, talks about a couple living without recognition from society until an incident of public concern draws them into the spotlight. Linda is a person with a disability of Multiple Sclerosis. Mark is her husband and he is facing charges of neglect to provide the necessities of life, after Linda was brought to the hospital under a medical emergency that almost took her life. The oppression model developed by Franz Fanon and others conceptualizes oppressed people suffer by being disenfranchised and they become invisible to the dominant society (Rothman, 203 p 9). Linda and Mark were invisible until this article was written. The media might not have the power to determine what people think, but they do determine what people think about (Neunedorf, 1990 P. 115). This article portrays Linda as helpless, and at the mercy of her incompetent, husband Mark. This newspaper article is more about what is not reported than what is reported.
Multiple Sclerosis affects about one in 500-1000 people in Canada and is more common in women. Symptoms are weakness, numbness and tingling, extreme fatigue, muscle spasticity, shaking and loss of coordination, poor balance and unsteadiness, difficulty talking and swallowing, depression, pain, memory loss, lack of concentration and problem solving, vision loss and changes, vertigo or dizziness, bladder and bowel issues, and sexual problems. The symptoms associated with this disease vary and different people are individually affected in different ways (C-Health. 1996-2007). This is a very important fact when addressing any person with a disability because each person is an individual and will not have the same personal experience as anot...
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...ervice and care from a social worker that incorporates the social model approach could help the couple engage in a caring relationship with professionals in the community that can bring assistance with their needs and help the couple find a way to become socially active. Rothman articulates that it is often harder to make friends and get around (Rothman, 2003 p 10). This could remove Linda and Mark from isolation that is often associated with a person with a disability and their caregivers. Their dignity and worth would be dignified in accordance with the Social work code of ethics. Implications surrounding this newspaper article choose to focus on the negative aspects of a person with a disability, but a collaboration of issues has contributed to the situation. Societal issues of neglect, ignorance, and aloofness contributed to the exclusion and care for Linda.
For future practice in social work, I learned that it is important to empower your clients to set goals and help push them to reach those goals. Robert wanted to plays sports and kept trying until he found a sport that was the best fit for him. Snow (2013a) talked about “the ‘problem’ of disability is not within the person, but within the social attitudes, and our attitudes shape the world we live in” (p.119). I agree with Snow, if our attitudes in society don’t change about “disabilities” the person will never feel completely welcomed or “fit” for
Joan L. Griscom outlines the struggles of oppression faced by the couple Sharon Kowalski and Karen Thompson in her article “The Case of Kowalski and Thompson: Ableism, Heterosexism, and Sexism”. The injustices these women faced were due to exactly that: ableism, heterosexism, and sexism. With Karen Thompson’s help, her and Sharon’s story is brought to light and shows that fighting the system can lead to making things right. Ableism was the first mode of oppression the women faced.
All these and more evidences used in the book support Peterson’s thesis and purpose—all of them discuss how having a disability made Peterson and others in her situation a part of the “other”. Her personal experience on media and
...to the situations and problems in social work. Poverty had a few chapters on its own. There is nothing wrong with covering poverty, but chapter thirteen should be split into two chapters to give a more comprehensive overview of developmental disabilities. Therefor the book should not exclude the chapter, it should expand the chapter. Developmental disabilities is constantly overlapping in social work. Social workers should have a basic understanding of developmental disabilities. Clients who have disabilities should be understood to an extent, and should get the help they need. The information in chapter thirteen does give helpful information in understanding individuals with developmental disabilities.
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
Multiple sclerosis - is an autoimmune disorder that affects the central nervous system including the spinal cord and brain.
According to National Multiple Sclerosis Society, Multiple Sclerosis (MS) is an unpredictable, often disabling disease of the central nervous system (CNS) that disrupts the flow of information within the brain, and between the brain and body. The central nervous system (CNS) comprises of the brain and the spinal cord. CNS is coated and protected by myelin sheath that is made of fatty tissues (Slomski, 2005). The inflammation and damage of the myelin sheath causing it to form a scar (sclerosis). This results in a number of physical and mental symptoms, including weakness, loss of coordination, and loss of speech and vision. The way the disease affect people is always different; some people experience only a single attack and recover quickly, while others condition degenerate over time (Wexler, 2013). Hence, the diagnosis of MS is mostly done by eliminating the symptoms of other diseases. Multiple sclerosis (MS) affects both men and women, but generally, it is more common in women more than men. The disease is most usually diagnosed between ages 20 and 40, however, it can occur at any age. Someone with a family history of the disease is more likely to suffer from it. Although MS is not
Nancy Mairs, born in 1943, described herself as a radical feminist, pacifist, and cripple. She is crippled because she has multiple sclerosis (MS), which is a chronic disease involving damage to the nerve cells and spinal cord. In her essay Disability, Mairs’ focus is on how disabled people are portrayed, or rather un-portrayed in the media. There is more than one audience that Mairs could have been trying to reach out to with this piece. The less-obvious audience would be disabled people who can connect to her writing because they can relate to it. The more obvious audience would be physically-able people who have yet to notice the lack of disabled people being portrayed by the media. Her purpose is to persuade the audience that disabled people should be shown in the media more often, to help society better cope with and realize the presence of handicapped people. Mairs starts off by saying “For months now I’ve been consciously searching for representation of myself in the media, especially television. I know I’d recognize this self becaus...
The Australian Association of Social Workers (AASW) Code of Ethics (2010) proposes three core values of Social Work, respect for persons, social justice and professional integrity (pp.12). These core values establish “ethical responsibilities” for the social worker (AASW, 2010, pp.12), specifically, the value of respect for persons, which sustains the intrinsic worth of all human beings as well as the right to wellbeing and self determination consistent with others in society (AASW, 2010,p.12). This Code of Ethics stipulates the duty of care a social worker must provide, a...
Primarily, the term MS refers to a chronic disorder that attacks the central nervous system (CNS). It is most common in temperate continents such as Europe and Australia with Asiatic and African continents having a lower risk of the disease (Wiley Online Library, 2013). A search organised by the Multiple Sclerosis Society (2013) has estimated that there are 127,000 people living with MS in the United Kingdom. Further research by Chipps, Clanin, and Campbell (1992, pp. 158-167) shows that MS disorder more likely affects women than men with its symptoms occurring between the ages of 20 and 40 in most cases and is quite uncommon in childhood and old age. The nerve cells known as neurons in the brain constantly transmit and receive signals. They invoke emotions, activities and cognition that constitute the day to day experiences of humans. Under normal circumstances, these signals travel on a protected insulation path known as the myelin sheath. This insulation is vital as it enables signals to reach their target. In Multiple Sclerosis, the myelin sheath gets disintegrated causing the nerve fibre to be damaged leading to a disruption in the abili...
The strengths perspective of social work focuses and utilises the assets family members possess to minimise their difficulties. Social workers are mindful of diversity and, to prevent bias, remain non-judgmental and respectful of families varying norms, values and attitudes, as well as have awareness of the potential of their own values influencing practice. As in many families with parents with relatively low care needs the high cost of assisted care means caring tends to befall upon daughters because of gender inequality and the assumption that females are more nurturing. In the story, Lydia had a strained relationship with her mother, but is was unthinkable for her father and brother to care for Alice as their role was as financial providers for the family’s needs. Consequentially, although Alice felt guilt and a burden to the family, Lydia adopted the role of primary carer, partially out of love and loyalty for her mother, but also necessity due to the family’s traditional views of gender. Although caring and supporting Alice with her mental ill-health needs enabled Lydia and her mother to repair and rekindle a closer relationship. Lydia tailed communication around Alice’s capabilities and through being honest and open, Lydia began to understand Alice as she could empathise with her mother’s plight and its emotional effect.
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.
Her scientific casework methods are still used in assessing clients in today’s practice. The Social Work profession also built off her values of individuality, dignity, and importance of human relationships in the core values of the profession, these can be seen in the National Association of Social Workers’ Code of Ethics. While Social Workers still follow most of Richmond’s values today, other values have been re-evaluated as time has progressed. Instead of Richmond’s suggestions of gathering personal information without the client’s knowledge (Pumphrey, 1961), the Social Work profession now values confidentiality and privacy when dealing with clients.
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.
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...