What 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 how they 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.
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