Discrimination Against People With Multiple Sclerosis
Kevin is a quiet man who has known he has multiple sclerosis (MS) for six years. He hasn\'t told anyone. [Kevin explains] “I went to a doctor because I had a serious fall. He decided to run some tests and a week later he told me that I have MS. No one can tell when they look at me. I\'ve learned how to cover losing my balance. I\'m only thirty-two. I\'m not going to tell anyone because they might think I can\'t do my job. I\'m sure not going to tell any woman I want to date. What\'s she going to think—I\'m a cripple?” (qtd. in “Disclosure”) This story is a prime example of what people who have MS live with every day of their lives. Kevin’s initial reaction was not concern for his health or well-being, but the kind of discrimination he would now have to face because of this devastating disease. People with MS are discriminated against in several aspects of life. According to the National Multiple Sclerosis Society (NMSS) Web page, MS is a disease that affects the brain and the spinal cord. When a person has MS the tissue called myelin which protects the nerves are damaged. The damage to the myelin is called “sclerosis,” commonly known as
People who suffer from MS are people who can not afford health benefits for many reasons. Many of them are facing the need to been on some sort of disability. Another way in which people with MS are discriminated against is in healthcare. The NMSS informs us that “many members of Congress believe that the current budget deficit requires limitation of prescription drug coverage to low-income beneficiaries… others believe a universal benefit is needed and that incremental steps to limit drug coverage to low-income beneficiaries will reduce the likelihood that Congress will enact a universal Medicare benefit in the future.” However, in most cases disability benefits are not granted immediately creating monetary hardship (Shaw). “Of MS patients who were diagnosed with the disease more than five years ago, 49 percent are not taking drugs…the Harris poll interviewed 562 MS patients and 251 neurologists who treat MS patients. In addition to the patients who weren’t taking drugs because they didn’t have physical symptoms of the disease, 32 percent said they couldn’t afford the medicine”(Neenan). This is a continuous problem for suffers of MS. According to the NMSS Congress is unlikely to pass any form of Medicare prescription coverage in the coming year (“Advocacy”). Unfortunate for many MS suffers discrimination in healthcare will be an on-going battle that does not seem to be ending in the near future. scar tissue, and “multiple” means many. These scars impair the activity of the nerves, by making it difficult for commands to reach and leave the brain. This causes the different symptoms of MS (“What is MS”). According to the NMSS approximately one third of a million Americans acknowledge having MS (“About MS”). Further people with MS are discriminated against in the workplace. Th
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Approximate Word count = 1240
Approximate Pages = 5 (250 words per page double spaced)
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