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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.
People today are not only living longer, they are also living sicker-- making aging and caring for elderly loved ones more complicated than ever before. Brent provides a comprehensive, straightforward handbook to help family caregivers with sibling and parent-child communication, end-of-life decision making, and guidance for how to help a loved one medically, financially, and emotionally.
These are collections of Mike Fileys best work from his popular and long-running Toronto Sun column, "The Way We Were."
"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 NEW YORK TIMES BESTSELLER! "I had the choice to come back ... or not. I chose to return when I realized that 'heaven' is a state, not a place" In this truly inspirational memoir, Anita Moorjani relates how, after fighting cancer for almost four years, her body began shutting down—overwhelmed by the malignant cells spreading throughout her system. As her organs failed, she entered into an extraordinary near-death experience where she realized her inherent worth . . . and the actual cause of her disease. Upon regaining consciousness, Anita found that her condition had improved so rapidly that she was released from the hospital within weeks—without a trace of cancer in her body! Within this enhanced e-book, Anita recounts—in words and on video—stories of her childhood in Hong Kong, her challenge to establish her career and find true love, as well as how she eventually ended up in that hospital bed where she defied all medical knowledge. In "Dying to Be Me," Anita Freely shares all she has learned about illness, healing, fear, "being love," and the true magnificence of each and every human being!
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.
When a Stage 4 lung cancer diagnosis upends longtime nurse Sharon Eagle's life, she discovers just how much her illness can teach her--about priorities, trust, and the joyful reconciliation of broken relationships.
Theresa conquered many hurdles in her lifetime, with victorious highs and shattering lows, but at fifty-four years old, she took on the biggest challenge of her life: advanced stage pancreatic cancer. Like most families, there are those times when moments in life tend to strain or burden relationships. Theresa chose humor in the face of death. Confronting her fate with grace, she taught everyone the true meaning of living life without regret. To those who loved her, she gave an amazing gift--showing them how to move past the sadness and truly enjoy the precious time she had left. Annette, her baby sister, didn't realize her strength until she held her sister's life in her hands. As a writer, she did the one thing she thought would have the most impact. She picked up a notebook and chronicled the journey with Theresa, revealing the strength and inspiration of an amazing woman. The two siblings shared a room as kids, and in the end, it was the same. A week or so before Theresa died, she told Annette, "This has been the best year of my life." Most people would have thought she was crazy, but her little sister knew exactly what she meant. The Other Side of Cancer: Living Life with My Dying Sister is a passionate story of two sisters and their extraordinary bond and friendship reignited in the face of cancer.
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.