A guide to proactively prepare for the end of life covers topics ranging from financial planning and medical issues to emotional considerations, with advice on health care proxies, wills, funeral preparations, and palliative care.

Most readers know Jane Brody as a staunch advocate of living a healthy life, to the fullest. But even the healthiest of lives end. This guide will help readers proactively make that end as peaceful, and even enjoyable, as it can be. From financial planning, important medical issues, to the oft-overlooked emotional considerations, Jane Brody shows that preparing for the end of life goes far beyond writing a will.

From the beloved New York Times columnist, trusted authority on health, and bestselling author comes this complete guide to everything you need to know–emotionally, spiritually, and practically–to prepare for the end of life. An invaluable road map to putting your affairs in order–or helping your loved ones do the same–this comprehensive book will answer every question you might have about what does and does not help smooth the transition between life and the Great Beyond. Wise, practical, and characteristically straightforward throughout, Brody advises on • the intricacies of a well-thought-out (and fully spelled-out) living will that health care practitioners readily understand–and how to designate a health care proxy. • planning a funeral or memorial to ensure your wishes are followed, including tips on how to reduce expenses. • discussing prognoses and treatment options with doctors. • your options for controlling pain, shortness of breath, bed sores, and other physical symptoms–plus the facts on feeding tubes. • receiving the support you need through hospice care–and suggestions for loved ones and friends who want to help. • lightening and enlightening your trials by incorporating spirituality into your life. • understanding what happens, physically and mentally, when death is imminent, and recognizing when hand-holding and reassurance, not food or drink or an oxygen mask or CPR, is the proper course of action. • easing your way through the journey of grief by admitting the reality of the loss, showing your emotions, and allowing yourself the time you feel you need. No matter your age or current health, preparing for the inevitable when you are still fully in control of your faculties ensures that you’ll be in a far better position to enjoy the time you have left. As Brody notes, “From the start, consider the finish.”

One of the most devastating losses a family can experience is the loss of a child. Whether the loss is through illness, accident, drugs, suicide, or other tragedy, the pain is overwhelming and often paralyzing. Often we think of "loss" as death. However, in our broken world there are many ways to suffer the loss of a child. This book discusses how a family can learn to cope with loss of a child due not only to death, but also to a custody battle, addiction (and other choices a child makes), chronic illness, crime (human trafficking, kidnap), and other issues where hopes and dreams disappear. Wright helps readers through the grieving process and assists them in finding God's grace and comfort during this very difficult time of life. This book is unique as it is for parents as well as grandparents.

Tapping the collective wisdom of the young adult cancer community Each year, nearly 70,000 young adults between 18 and 40 are diagnosed in the United States with cancer. While there are many sources of information for patients, the special concerns of this age group are rarely discussed. One remarkable exception is PlanetCancer.org. For nearly a decade, those in this “gap” age have sought out this online community for resources, networks, and support from those who have been there and done that. Planet Cancer is an honest, down-to-earth guide to living in this new world, from Diagnosis to Post-Treatment. Each chapter is informed by Planet Cancer's voice—authoritative, funny, friendly, no-nonsense. Experts address issues from all sides around bedrock “What It's Really Like” essays: deeply personal, unflinching, and often hilarious pieces written by people who actually experienced on Planet Cancer things like banking sperm, adopting a child, or undergoing brain radiation. The book, enlivened with quotes and real-life stories from Planet Cancer members, gives the uninitiated a sense of community and removes some of the mystery and fear of the unknown. Planet Cancer is now a LIVESTRONG initiative.

This novel, cross-disciplinary collection explains how dying, death, and grieving have changed in America, for better or worse, since the turn of the millennium. What does dying with dignity mean in a diverse society with rapidly advancing technology, an aging population, and finite resources? In this fascinating collection, scholars from across the nation illuminate the remarkable changes that have taken place in recent years, are now underway, and loom on the horizon as they lead readers on an exploration of the ways Americans think about and handle dying and death. Volume 1, New Paths of Engagement, addresses changes in the circumstances and expressions of death, dying, and grief in 21st-century America. Volume 2, New Venues in the Search for Dignity and Grace, delves into the challenges inherent in creating a medical and social system that allows for an optimal end-of-life experience for all and proposes ways in which society can be reshaped to move toward that ideal.

The Oxford Textbook of Palliative Social Work is a comprehensive, evidence-informed text that addresses the needs of professionals who provide interdisciplinary, culturally sensitive, biopsychosocial-spiritual care for patients and families living with life-threatening illness. Social workers from diverse settings will benefit from its international scope and wealth of patient and family narratives. Unique to this scholarly text is its emphasis on the collaborative nature inherent in palliative care. This definitive resource is edited by two leading palliative social work pioneers who bring together an array of international authors who provide clinicians, researchers, policy-makers, and academics with a broad range of content to enrich the guidelines recommended by the National Consensus Project for Quality Palliative Care.