The first resource on end-of-life care for healthcare
practitioners who work with the terminally ill and their families,
"Living with Dying" begins with the narratives of five healthcare
professionals, who, when faced with overwhelming personal losses
altered their clinical practices and philosophies. The book
provides ways to ensure a respectful death for individuals,
families, groups, and communities and is organized around
theoretical issues in loss, grief, and bereavement and around
clinical practice with individuals, families, and groups.
"Living with Dying" addresses practice with people who have
specific illnesses such as AIDS, bone marrow disease, and cancer
and pays special attention to patients who have been stigmatized by
culture, ability, sexual orientation, age, race, or homelessness.
The book includes content on trauma and developmental issues for
children, adults, and the aging who are dying, and it addresses
legal, ethical, spiritual, cultural, and social class issues as
core factors in the assessment of and work with the dying. It
explores interdisciplinary teamwork, supervision, and the
organizational and financing contexts in which dying occurs.
Current research in end-of-life care, ways to provide leadership
in the field, and a call for compassion, insight, and respect for
the dying makes this an indispensable resource for social workers,
healthcare educators, administrators, consultants, advocates, and
practitioners who work with the dying and their families.
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