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Item Details
Title: IN THE SHADOW OF ILLNESS
PARENTS AND SIBLINGS OF THE CHRONICALLY ILL CHILD
By: Myra Bluebond-Langner
Format: Hardback

List price: £39.95


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ISBN 10: 0691027838
ISBN 13: 9780691027838
Publisher: PRINCETON UNIVERSITY PRESS
Pub. date: 3 November, 1996
Pages: 328
Description: This text suggests that understanding the impact of the illness of a chronically ill child on their family lies not in identifying deficiencies in the lives of those affected, but in appreciating how family members carry on with their lives in the face of the disease's intrusion.
Synopsis: "This book powerfully illuminates the everyday experience of families living with a chronicallyill child."--Patricia A. Marshall, Associate Director of Medical Humanities Program at Loyola University Chicago, Strich School of MedicineWhat is it like to live with a child who has a chronic, life-threatening disease? What impact does the illness have on well siblings in the family? Myra Bluebond-Langner suggests that understanding the impact of the illness lies not in identifying deficiencies in the lives of those affected, but in appreciating how family members carry on with their lives in the face of the disease's intrusion.The Private Worlds of Dying Children, Bluebond-Langner's previous book, now considered a classic in the field, explored the world of terminally ill children. In her new book, she turns her attention to the lives of those who live in the shadow of chronic illness: the parents and well siblings of children who have cystic fibrosis. Through a series of narrative portraits, she draws us into the daily lives of nine families of children at different points in the natural history of the illness--from diagnosis through the terminal phase. In these portraits, as family members talk about their experiences in their own words, we see how parents, well siblings, and the ill children themselves struggle, in different ways, to contain the intrusion of the disease into their lives.Bluebond-Langner looks at how parents adjust their priorities and their idea of what constitutes a normal life, how they try to balance the needs of other family members while caring for the ill child, and how they see the future. This context helps us understand how well siblings view the illness and howthey relate to their ill sibling and parents. Since the issues raised are not unique to cystic fibrosis but are common to other chronic and life-threatening illnesses, this book will be of interest to all who study, care for, or live with the seriously ill.
Illustrations: 3 tables
Publication: US
Imprint: Princeton University Press
Returns: Non-returnable
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