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Dying at Home: A Family Guide for Caregiving (Johns Hopkins Press Health Books)
  
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Dying at Home: A Family Guide for Caregiving (Johns Hopkins Press Health Books) [Hardcover]

Professor Andrea Sankar (Author)


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Book Description

0801862027 978-0801862021 September 10, 1999 Revised

A growing number of people choose to live their final weeks or months at home. For patients who cannot benefit from acute care in the hospital, home care offers an alternative to a nursing home or hospice. Advances in medical technology and pharmacology allow even those with serious illnesses to remain at home relatively free of pain and symptoms, and professional services are increasingly available to assist family caregivers with work that is often physically and emotionally exhausting.

First published in 1991, Dying at Home examined the reasons behind this trend and offered practical advice about assuming as much control as possible over the process of dying. In this thoroughly updated edition, medical anthropologist and gerontologist Andrea Sankar keeps her focus on the patient and loved ones while providing the latest information on hospice home care teams, pain medications, HIV and AIDS, legislation on death with dignity, physician-assisted suicide, and sources of information and support for patients and families.

Dying at Home is an intimate account based on extensive interviews with family and professional caregivers as well as with other family members, friends, and patients. The author addresses the concerns and problems of those who face the decision of whether to care for a dying loved one at home, including preparing the home environment for caregiving; how to use professional caregivers in the home setting; managing the patient's pain, agitation, and other conditions; and how to recognize impending death and what to do immediately after death. She draws from stories that represent a wide range of circumstances and causes of death.

At home, surrounded by family and friends in a comforting environment, patients have some control over what remains of their lives. "Home death is a powerfully significant experience," the author writes, "despite the strain, exhaustion, and conflict that sometimes accompany it. Its power lies in the fact that in the face of certain death, the caregiver can give the person life, that is, the continuation of life as a social being."

Praise for Dying at Home:

"A wealth of practical information and thoughtful discussion."--Milwaukee Journal

"Begins to fill our deficit of experience with accurate information and compassionately told stories." -- San Francisco Chronicle

"The author combines her professional knowledge of home care with her personal experience of caring for her dying mother at home. The result is a concise volume geared to the lay person that presents a clear picture of the issues, problems, and accomplishments arising from the patient's decision to die at home and the special role of the patient's caregiver."--Cathy Coyle, Social Work in Health Care

"One of the book's most appealing features, beyond its sympathetic yet straightforward manner, is that it reports research while including helpful hints and extensive quotations from actual caregivers."--Jeanne E. Bader, Aging Today

"Andrea Sankar tells us we have not solved the problem of caregivers' pain... She gives voice to the caregivers of dying patients and highlights their concerns... Andrea Sankar may be the Benjamin Spock for care of the terminally ill."--Priscilla Kissick, Hospice Journal

"This book is meant for lay readers, but could serve as a valuable resource for health care professionals. It is an outstanding reference for the physician to recommend to the family or caregiver of the patient who wants to die at home. Using a variety of illustrative case studies, Dying at Home provides useful and practical guidance for the caregivers of a dying family member or friend."--Joseph R. Stenger, Journal of Family Practice


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Editorial Reviews

From Publishers Weekly

Sankar's book is more than just a practical how-to for those who are caring for the terminally ill at home. It is also a deeply moving, painfully honest look at the experience of tending a dying loved one. Drawing on her home-care expertise and training as a medical anthropologist, Wayne State University professor Sankar (coauthor of The Home Care Experience ) interviewed 13 caregivers. What's essential, say she and her subjects, is to give patients "the recognition that they are still among the living." The process can provide families with a sense of intimacy and empowerment they might never feel in a hospital setting. Chapters are organized around significant issues discussed by the caregivers: the decision to take the patient home to die, use of professional help in the home, caregiving and social support, and death. All of the caregivers evidently felt that they were not "special" because of their efforts. They were beneficiaries, too. "Home death is a powerfully significant experience. . . . Its power lies in the fact that . . . the caregiver can give the person life, that is, the continuation of life as a social being."
Copyright 1991 Reed Business Information, Inc. --This text refers to an out of print or unavailable edition of this title.

From Library Journal

Sankar, a medical anthropologist and co-editor of The Home Care Experience: Ethnography and Policy (Sage Pubns., 1990), has written a book on home death for those already caring for a terminally ill loved one at home or those considering it. The author examines the physical, social, and emotional toll involved and illuminates each topic--discharge to home, formal and informal support, caregiving, signs of death, and after death--with apt and often moving observations made by people who experienced the home death of a child, parent, or spouse or companion. Recommended for health, hospice, gerontology, and larger general collections. See also Harry A. Cole's Helpmates: Support in Times of Chronic Illness, reviewed in this issue, p. 105.--Ed.
- Anne C. Tomlin, Auburn Me morial Hosp . Lib., N.Y.
Copyright 1991 Reed Business Information, Inc. --This text refers to an out of print or unavailable edition of this title.

Product Details

  • Hardcover: 328 pages
  • Publisher: The Johns Hopkins University Press; Revised edition (September 10, 1999)
  • Language: English
  • ISBN-10: 0801862027
  • ISBN-13: 978-0801862021
  • Product Dimensions: 9.1 x 6.1 x 1.2 inches
  • Shipping Weight: 1.4 pounds
  • Amazon Best Sellers Rank: #5,877,830 in Books (See Top 100 in Books)

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Inside This Book (learn more)
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First Sentence:
"We did it!" exclaimed one woman after her husband died at home. Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
disciplinary subcommittee, patient surrogate, amendatory act, dying person, recommended medical treatment, hospice agency, hospice personnel, discharge planner, home care agency, patient log, hospice benefit, main caregiver, home death, medical treatment decisions, home care agencies, venous access device, external catheter
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Elizabeth Krolick, John Wright, Visiting Nurse Association
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