Caring for a loved one who is terminally ill can be tremendously stressful under any circumstances. If that person has a degenerative and dementing disease such as Alzheimer's, and is unable to participate in decisions regarding his or her care, the stress is that much greater. When it comes to making those difficult moral and ethical decisions which will preserve the dignity and integrity of the patient while also maintaining the caregiver's own selfhood, this is the book that can help.How much should the patient be told? How strongly should he be urged to plan for his own future? Is it ever right to lie to the patient about her condition? When is it right to place your loved one in a nursing home--and not feel guilty about it? How do different family members arrive at agreement among themselves in each of these situations?Authors and bioethicists James and Hilde Lindemann Nelson have written an invaluable step-by-step guide to tackling these and other difficult decisions. Using their extensive research on moral issues in health care, the Nelsons create hypothetical scenarios that demonstrate some of the most common situations caregivers will have to face during every stage of the illness, and show by example how they can make the right choices for themselves, the patient, and the rest of the family. This invaluable information, combined with a state-by-state and city-by-city guide to agencies and support groups offering practical assistance, as well as a list of suggested reading on the subject, make this book unique--and the most complete source of advice available.
From the Hardcover edition.
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Authors and bioethicists James and Hilde Lindemann Nelson have written an invaluable step-by-step guide to tackling these and other difficult decisions. If that person has a degenerative and dementing disease such as Alzheimer's, and is unable to participate in decisions regarding his or her care, the stress is that much greater. When it comes to making those difficult moral and ethical decisions which will preserve the dignity and integrity of the patient while also maintaining the caregiver's own selfhood, this is the book that can help. How much should the patient be told?
Nelson, James Lindemann & Hilde Lindemann Nelson. Alzheimer's: Answers to Hard Questions for Families .
Nelson, James Lindemann & Hilde Lindemann Nelson. The Nelsons write clear, untechnical prose with an uncommonly fine eye for detail, and the case descriptions are superb. -John Hardwig, East Tennessee State University. Their critique of the current dogmas that tend to guide medical decision-making in the care of incompetent patients is very powerful.
by James Lindemann Nelson and Hilde Lindemann Nelson. A Useful Guide to Alzheimer's. com User, June 11, 1999
by James Lindemann Nelson and Hilde Lindemann Nelson. com User, June 11, 1999. Answers to Hard Questions for Families guides readers through the difficult moral and ethical problems any family dealing with the disease will have to face.
Similar books and articles. The Patient in the Family: An Ethics of Medicine and Families, Hilde Lindemaiin Nelson and James Lindemann Nelson. Hilde Lindemann Nelson & Daniel Callahan - 2005 - Hastings Center Report 35 (4):15-16. Lindemann Hilde & Nelson James Lindemann - 2008 - Hastings Center Report 38 (4):19-21. New York: Routledge, 1995.
Alzheimer's: Answers to hard questions for families, James Lindemann Nelson and Hilde Lindemann Nelson. Authors and affiliations.
Nelson, James Lindemann; Nelson, Hilde Lindemann. Alzheimer's disease - Popular works, Alzheimer's disease - Patients - Family relationships, Caregivers, Alzheimer's disease. New York : Main Street Books. inlibrary; printdisabled; ; ctlibrary; china; americana.
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Lindemann Nelson, Hilde; Lindemann Nelson, Jamie (1995). The patient in the family. Lindemann Nelson, Hilde; Lindemann Nelson, Jamie (1996). In Dutch translation, Amsterdam: De Arbeiderspers, 1998. Lindemann Nelson, Hilde; Lindemann Nelson, Jamie (1999). Retrieved 2016-04-04. Moody, Harry (Jun 1, 1998). The Journal of Value Inquiry. Lindemann, Hilde Theoretical Resources for a Globalized Bioethics.