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Viewing Alzheimer's disease through new lenses: Protecting personhood, combating stigma, and preserving decision-making capacity.

机译:通过新的视角观察阿尔茨海默氏病:保护人格,对抗耻辱感并保留决策能力。

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摘要

Alzheimer's disease (AD) is an incurable chronic neurodegenerative disorder. Since there is no cure for AD, the focus of the disease is negative and hopeless. A negative view of AD poses problems; it strips individuals with the disease of their personhood, perpetuates personal and societal stigma, and removes autonomous decision-making capacity from those with AD.;Some philosophers have included memory and cognition as criteria for personhood, placing persons with AD at risk for losing their status as persons. Further, our culture strongly values cognition, intellect, and independence, and fears anything that erodes those principles. Therefore, our society fears AD. As a consequence, society tends to discriminate against, stereotype, and devalue those suffering from the disease. When stigma and stereotyping occurs, this further reinforces the lack of personhood of those with the disease. Our culture also values autonomy. It is traditionally believed that when a person experiences cognitive deficits, he or she needs a third party to make legal and medical decisions. Persons with AD can exert previous autonomous wishes but problems arise when their previous wishes conflict with what is in their current best interests.;This dissertation examines the writings of philosophers throughout history to determine criteria for personhood, explores theories of stigma, and explores the narratives of persons with AD to gain an insight into how society treats them once they are diagnosed, and presents the bioethical standards for decision-making to apply them to persons with AD.;Disputing the belief that cognition and memory are sole criteria for personhood, this work explores cognitive capacities that remain in a person throughout the course of AD, identifies other criteria for personhood, and discusses how the loss of one's memory affects personal identity, but not one's status as a person. Finally, it proposes a model for decision-making that honors a person's current autonomy and considers his or her best interests, and offers a new way for our society to view AD, a view that brings hope rather than despair.
机译:阿尔茨海默氏病(AD)是一种无法治愈的慢性神经退行性疾病。由于无法治愈AD,因此该疾病的重点是消极且无望的。对AD的否定看法会带来问题。它剥夺了患有人格障碍的人,使个人和社会的耻辱永久化,并消除了患有AD的人的自主决策能力。;一些哲学家将记忆和认知作为人格的标准,从而使患有AD的人有失去自己的风险身份。此外,我们的文化强烈重视认知,智力和独立性,并惧怕侵蚀这些原则的任何事物。因此,我们的社会担心公元。结果,社会趋向于歧视,刻板印象和贬低那些患有该疾病的人。当出现污名和陈规定型观念时,这进一步加剧了患有这种疾病的人的缺乏人格。我们的文化也重视自治。传统上认为,当一个人遇到认知缺陷时,他或她需要第三方做出法律和医疗决定。患有AD的人可以行使先前的自主愿望,但是当他们的先前愿望与他们当前的最大利益冲突时,就会出现问题。;本论文研究了整个历史上哲学家的著作,以确定人格标准,探讨了污名化的理论,并探讨了叙事的AD患者了解被诊断出的社会如何对待他们,并提出了将其应用于AD患者的决策的生物伦理标准。认为认知和记忆是人格的唯一标准,这项工作探索了整个AD过程中人的认知能力,确定了其他人格标准,并讨论了记忆力的丧失如何影响个人身份,而不影响人的身份。最后,它提出了一种决策模型,该模型应尊重一个人当前的自主权并考虑他或她的最大利益,并为我们的社会提供一种看待广告的新方式,这种看法带来希望而不是绝望。

著录项

  • 作者

    Wesner, Susan B.;

  • 作者单位

    Drew University.;

  • 授予单位 Drew University.;
  • 学科 Gerontology.;Philosophy.;Sociology Social Structure and Development.
  • 学位 D.M.H.
  • 年度 2010
  • 页码 180 p.
  • 总页数 180
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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