Living And Dying With Cancer

Living and Dying with Cancer is a powerful and moving account of the experiences of those affected by one of the most common causes of death in the Western world. Through a series of individual narratives based on extensive interviews carried out by the author, the book explores the impact of being diagnosed with cancer on those with the disease and the people around them. It follows the different trajectories of the disease from the very first symptoms, through treatment to death and shows how the experience of the disease and even the way it develops is affected by the social context of the people involved, as well as their own physical and psychological characteristics. This book will be an invaluable resource not only for social scientists and health professionals but also for those coming to terms with the impact of cancer on their own lives.

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.

Explores the impact of cancer on those with the disease and the people around them.

How can anyone feel hopeful after learning she is fatally ill? Sharon Eagle seeks to answer that very question in Terminal Hope, which chronicles her experience with stage 4 lung cancer. After receiving her diagnosis, Eagle, a longtime nurse and educator, understands immediately that her cancer will probably kill her. What she can’t foresee is the remarkable wisdom she gains from the spiritual and emotional quest that her diagnosis sparks. As she navigates the land of cancer, seeking new purpose and meaning, Eagle discovers that her illness has a great deal to teach her. Among many other lessons, cancer inspires her to examine her own faith journey, rebuild relationships, and reconsider patient-caregiver communication and support. Above all, she uncovers compelling evidence for her belief that death is not the end but rather merely a transition to something even better. A moving memoir about the power of positivity, gratitude, and faith, Terminal Hope offers a new perspective for people of all belief systems.

"Built on her ... Modern Love column, 'When a Couch is More Than a Couch' (9/23/2016), a ... memoir of living meaningfully with 'death in the room' by the 38-year-old great-great-great granddaughter of Ralph Waldo Emerson--mother to two young boys, wife of 16 years--after her terminal cancer diagnosis"--

The author, a successful businessman, describes his seven-year struggle against cancer, recounts his experiences with surgery and chemotherapy, and explains how the disease has affected his family life.