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Author: Alan Meisel
Publisher: Wolters Kluwer
ISBN: 0735546657
Category : Law
Languages : en
Pages : 2023
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Book Description
The Right to Die, Third Edition analyzes the statutory and case law
Author: Alan Meisel
Publisher: Wolters Kluwer
ISBN: 0735546657
Category : Law
Languages : en
Pages : 2023
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Book Description
The Right to Die, Third Edition analyzes the statutory and case law
Author: Anne Kenny
Publisher: JHU Press
ISBN: 1421426684
Category : Health & Fitness
Languages : en
Pages : 232
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Book Description
Making Tough Decisions about End-of-Life Care in Dementia is a lifeline, an invaluable guide to assist in the late stage of dementia.
Author: Nancy Berlinger
Publisher: Oxford University Press
ISBN: 0199974578
Category : Medical
Languages : en
Pages : 265
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Book Description
This major new work updates and significantly expands The Hastings Center's 1987 Guidelines on the Termination of Life-Sustaining Treatment and Care of the Dying. Like its predecessor, this second edition will shape the ethical and legal framework for decision-making on treatment and end-of-life care in the United States. This groundbreaking work incorporates 25 years of research and innovation in clinical care, law, and policy. It is written for physicians, nurses, and other health care professionals and is structured for easy reference in difficult clinical situations. It supports the work of clinical ethicists, ethics committee members, health lawyers, clinical educators, scholars, and policymakers. It includes extensive practical recommendations. Health care reform places a new set of challenges on decision-making and care near the end of life. The Hastings Center Guidelines are an essential resource.
Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 0309303133
Category : Medical
Languages : en
Pages : 470
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Book Description
For patients and their loved ones, no care decisions are more profound than those made near the end of life. Unfortunately, the experience of dying in the United States is often characterized by fragmented care, inadequate treatment of distressing symptoms, frequent transitions among care settings, and enormous care responsibilities for families. According to this report, the current health care system of rendering more intensive services than are necessary and desired by patients, and the lack of coordination among programs increases risks to patients and creates avoidable burdens on them and their families. Dying in America is a study of the current state of health care for persons of all ages who are nearing the end of life. Death is not a strictly medical event. Ideally, health care for those nearing the end of life harmonizes with social, psychological, and spiritual support. All people with advanced illnesses who may be approaching the end of life are entitled to access to high-quality, compassionate, evidence-based care, consistent with their wishes. Dying in America evaluates strategies to integrate care into a person- and family-centered, team-based framework, and makes recommendations to create a system that coordinates care and supports and respects the choices of patients and their families. The findings and recommendations of this report will address the needs of patients and their families and assist policy makers, clinicians and their educational and credentialing bodies, leaders of health care delivery and financing organizations, researchers, public and private funders, religious and community leaders, advocates of better care, journalists, and the public to provide the best care possible for people nearing the end of life.
Author: Jeff Spiess
Publisher: Rowman & Littlefield Publishers
ISBN: 1538141906
Category : Self-Help
Languages : en
Pages : 204
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Book Description
Death may be inevitable, but fearing the end-of-life is avoidable. Learn how to put your fear of your final days to rest. We all know we are going to die, but live as though we don’t believe it. Rather than explore our options and consider the possibilities that can impact our final days, we ignore the idea altogether out of fear. By avoiding the topic of death, we increase the pain and grief we experience at the end of life, and the suffering of those left behind. After three decades of caring for the dying, Dr. Jeff Spiess argues that if we honestly face our mortality, we will make wiser decisions, die with less distress, and live the remainder of our lives, whether days or decades, more fully and with less anxiety. Using cultural and religious references alongside poignant narratives, this optimistic work informs, inspires, and challenges our cognitive and emotional understandings of our own lives and deaths. Dying with Ease contains the practical nuts and bolts information about advance care planning, hospice, palliative care, and ethical and legal issues surrounding dying in America. Dr. Spiess answers such questions as: How can I plan for the last part of my life? What options do I have if my suffering is unbearable? What do religion and spiritual philosophy have to say about dying? What does it feel like to die? While dying can be difficult, it can also be beautiful. By learning to relax in the face of death at our current stage of life, we can make wiser and more authentic decisions throughout the rest of our lives-- however long they may be.
Author: James L. Werth Jr.
Publisher: Taylor & Francis
ISBN: 1135918848
Category : Education
Languages : en
Pages : 417
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Book Description
Decision Making near the End of Life provides a comprehensive overview of the recent developments that have impacted decision-making processes within the field of end-of-life care. The most current developments in all aspects of major underlying issues such as public attitudes, the impact of media, bioethics, and legal precedent provide the background information for the text. The authors examine various aspects of end-of-life choices and decision-making, including communication (between and among family, medical personnel, the dying person), advance directives, and the emergence of hospice and palliative care institutions. The book also explores a variety of psychosocial considerations that arise in decision-making, including religion/spirituality, family caregiving, disenfranchised and diverse groups, and the psychological and psychiatric problems that can impact both the dying person and loved ones. Case studies and first-person stories about decision-making, written by professionals in the field, bring a uniquely personal touch to this valuable text.
Author: Betty Ferrell
Publisher:
ISBN: 0190244186
Category : Family & Relationships
Languages : en
Pages : 161
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Book Description
Pediatric palliative care is a field of significant growth as health care systems recognize the benefits of palliative care in areas such as neonatal intensive care, pediatric ICU, and chronic pediatric illnesses. Pediatric Palliative Care, the fourth volume in the HPNA Palliative Nursing Manuals series, highlights key issues related to the field. Chapters address pediatric hospice, symptom management, pediatric pain, the neonatal intensive care unit, transitioning goals of care between the emergency department and intensive care unit, and grief and bereavement in pediatric palliative care. The content of the concise, clinically focused volumes in the HPNA Palliative Nursing Manuals series is one resource for nurses preparing for specialty certification exams and provides a quick-reference in daily practice. Plentiful tables and patient teaching points make these volumes useful resources for nurses.
Author: Bill Davis
Publisher: P & R Publishing
ISBN: 9781629952598
Category : Religion
Languages : en
Pages : 300
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Book Description
Decisions at the End of the create deep anxiety for those involved. But it is possible to find peace and comfort amid the hard choices. As a church elder and hospital ethics consultant, Bill Davis has talked, walked, and prayed with many people in end-of-life situations. Employing varied case studies and biblical, ethical insight, he guides you in making decisions for yourself and others, preparing advance directives, taking financial concerns into account, and navigating new realities in American hospitals Book jacket.
Author: Tom Wallace
Publisher: Createspace Independent Publishing Platform
ISBN: 9781542318051
Category :
Languages : en
Pages : 72
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Book Description
Who wants to think about dying? Most of us quickly answer that question, "Not me." Author Tom Wallace, however, has been contemplating how we die since the death of his first wife and his diagnosis with vascular dementia. For the past four years, he has been living day-to-day and grappling with the issues he writes about in this book. Making End-of-Life Decisions is the output of Tom's journey - the steps he's taken to remain in control of his life to the very end. Through the book, you'll understand how to create a "good death" which allows people to remain autonomy over how their life ends, as well as how to avoid a "bad death" in which others control when and how you die. With the help of Wallace and Making End-of-Life Decisions, you can learn how to make your wishes clear to loved ones, caretakers, and medical practitioners. How? You make your wishes clear through conversations, either verbally or in writing. His guide will teach you how to decide what a "good death'" means to you; start that initial conversation with your loved ones, medical team, and others; choose which kinds of end-of-life care you prefer; and prepare the documents that will help ensure that you get the care you desire. Never has the phrase "Plan Ahead" been more appropriate or more helpful.
Author: Ira Byock
Publisher: Penguin
ISBN: 110150028X
Category : Medical
Languages : en
Pages : 321
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Book Description
From Ira Byock, prominent palliative care physician and expert in end of life decisions, a lesson in Dying Well. Nobody should have to die in pain. Nobody should have to die alone. This is Ira Byock's dream, and he is dedicating his life to making it come true. Dying Well brings us to the homes and bedsides of families with whom Dr. Byock has worked, telling stories of love and reconciliation in the face of tragedy, pain, medical drama, and conflict. Through the true stories of patients, he shows us that a lot of important emotional work can be accomplished in the final months, weeks, and even days of life. It is a companion for families, showing them how to deal with doctors, how to talk to loved ones—and how to make the end of life as meaningful and enriching as the beginning. Ira Byock is also the author of The Best Care Possible: A Physician's Quest to Transform Care Through the End of Life.
