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Dying at Home: A Family Guide for Caregiving [Hardcover]

Professor Andrea Sankar (Author)


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Dying at Home: A Family Guide for Caregiving (Johns Hopkins Press Health Books) Dying at Home: A Family Guide for Caregiving (Johns Hopkins Press Health Books)
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Book Description

October 1, 1991 0801842301 978-0801842306 1
A powerful new movement is underway to return the dying to their own homes. This unique and much-needed book is for anyone who wonders what it would be like, and--for those who have made the decision--a comforting yet realistic guide to daily caregiving.

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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.

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.

Product Details

  • Hardcover: 280 pages
  • Publisher: The Johns Hopkins University Press; 1 edition (October 1, 1991)
  • Language: English
  • ISBN-10: 0801842301
  • ISBN-13: 978-0801842306
  • Product Dimensions: 9.1 x 6.1 x 1 inches
  • Shipping Weight: 1.3 pounds
  • Amazon Best Sellers Rank: #5,130,456 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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