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Books : Nonfiction : Law : Family & Health Law : Right to Die
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What has become known as the Schiavo affair-the death of a brain-damaged woman in Florida in 2005, and the controversy that surrounded it-was a revelatory moment in American society. For the first time, the nation got a clear view of both the fanaticism gripping the religious right and the political power it could bring to bear even when the vast majority of the country disagreed with it. But it was also a turning point: a moment when America seemed to glimpse a dangerous radicalism, and began to pull back. Eleanor Clift witnessed this event from a unique vantage point. At the same time that Schiavo was dying in her Florida hospice, Clift’s husband, Tom Brazaitis, was dying of cancer at home; the two passed away within a day of each other. Two Weeks of Life alternates between these two stories to provide a moving commentary on how we deal, or fail to deal, with dying in modern America.
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It often seems that medical technology is a never-ending string of miracles. But it is also a double-edged sword. More often than not, death today happens because of a decision to stop doing something, or to not do it at all. As the tragic life and death of Terri Schiavo so poignantly illustrated, universal definitions of life, death, nature, and many other concepts are elusive at best. Unplugged addresses the fundamental questions of the right-to-die debate, and discusses how the medical advances that bring so much hope and healing have also helped to create today’s dilemma.
Now in paperback, this compelling book illuminates the complex legal, ethical, medical, and deeply personal issues of a debate that ultimately affects us all. Compassionate and beautifully written, the book helps readers understand the implications of current laws and proposed legislation, various medical options (including hospice), and the typical end-of-life decisions we all must face in order to make informed decisions for ourselves and our loved ones.
The hardcover edition was chosen by The Library Journal as one of the Best Consumer Health Books of 2006.
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As the trial over her fate rages in a stately old courtroom in southwestern Missouri, the unmistakable voice of Ted Koppel tells the nation about Nancy Cruzan— "This is, at one and the same time, one of the simplest and one of the most complicated stories with which we have ever dealt." Long Goodbye: The Deaths of Nancy Cruzan follows an ordinary family’s extraordinary journey to the United States Supreme Court. The book looks behind the scenes at the painful human cost exacted in a highly public legal battle. It is the true story of an American tragedy—a tragedy that could visit any of us in an instant.
On a black January night Nancy Cruzan’s 20-year-old Rambler flies off the road and travels the length of two football fields before flipping to a stop. Nancy is thrown out face down on the cold ground, apparently dead. But not quite. Five years later, Nancy has not emerged from her coma, and her family makes the grim request that the state hospital remove Nancy’s feeding tube, which the family authorized years before when hope remained. But the state refuses, and the battle begins. Before the battle is over, powerful forces in society will team up to oppose the family—including the Missouri Attorney General, Missouri Governor John Ashcroft, United States Solicitor General Ken Starr, and the U.S. Conference of Catholic Bishops. Near the end, protestors from around the country converge on Missouri, and attempt to storm the hospital. Their fight reaches its climax, and resolution, shortly after midnight on a bitter cold Christmas Day. This blue-collar family keeps one goal from! beginning to end – trying to do what they know in their hearts their loved one would want them to do. In the process, they help to raise the consciousness of a nation, and "free countless Americans of some of the fears attending death," according to the New York Times.
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Assisted suicide remains one of the most emotionally charged and controversial topics—and the issue isn’t going away any time soon. As the baby boomer generation ages, many of us will watch as our parents—and ourselves—grow older, and wonder at the decisions that lie ahead.
Understanding Assisted Suicide provides both a fresh take on this important topic and the framework for intelligent participation in the discussion. Uniquely, the author frames the issue using his own experience watching both his parents die, which led him to ask fundamental questions about death, dying, religion, and the role of medicine and technology in alleviating human suffering.
In concerns about assisted suicide, each person’s “big picture” has largely been created out of picking and choosing from nine separate snapshot albums.
Understanding this offers a perspective for quickly determining the sources of another’s opinion on assisted suicide, as well as the issues they are not considering. Most importantly, Understanding Assisted Suicide offers a clear, easy-to-traverse landscape over which those who are sincerely looking for their own answers can navigate. The “nine-issue structure” allows both careful exploration of separate issues and a view of the full spectrum of ideas involved.
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One of the country's most distinguished scholars presents a brilliantly original approach to the twin dilemmas of abortion and euthanasia, showing why they arouse such volcanic controversy and how we as a society can reconcile our values of life and individual liberty.
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Explores the issue of euthanasia & the right to die. Poses the questions we should all ask ourselves & helps us determine the spiritual lessons that dying is meant to teach us. The Hippocratic Oath decrees that physicians prolong life & relieve suffering. However, technological advancements have blurred the lines between these issues. He rails against the inadequate treatment of physical pain & gives sensible medical & spiritual perspectives on chronic & terminal emotional & physical pain. Discusses the deeper meanings of life, death, suicide, & euthanasia. Asks whether we have the right to kill ourselves even though we have the power.
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After the Nancy Cruzan case was decided by the Supreme Court in 1990, and ultimately resolved by the Courts of the State of Missouri, the decision to withhold or withdraw life-prolonging nutrition and hydration appeared to many to be as noncontroversial as decisions to refuse respirators or dialysis. Even the Catholic Church held that, although there should be a presumption in favor of providing nutrition and hydration, the patient or the patient’s surrogate could overrule this presumption, if either believed the treatment was disproportionate or burdensome.
The Schiavo case changed all that. Although the decision to remove Terri Schiavo’s nutrition and hydration was made by her husband—her legal surrogate—based on his wife’s belief that such treatment was disproportionate, Schiavo’s immediate family protested so much that the case took years to resolve. It eventually involved all branches of government at both the state and federal levels.
The ethical dilemmas that such cases pose continue to stir great controversy. This in-depth examination of these dilemmas provides information and documentation from many perspectives. The editors have included a foreword by Dr. Jay Wolfson, Terri Schiavo’s court-appointed guardian ad litem, as well as Dr. Wolfson’s report to Gov. Jeb Bush on the case and Gov. Bush’s reply; public statements by President George Bush and Senators David Weldon, Rick Santorum, Tom DeLay, Bill Frist, and Barney Frank; statements by the pope and other representatives of the Catholic Church on this issue; plus much medical and legal background material on both precedents to the Schiavo case and its aftermath, including the results of the autopsy report.
For anyone wishing an in-depth understanding of these complex ethical issues, issues many of us will have to confront in our own families, this volume is indispensable.
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While it may seem that debates over euthanasia began with Jack Kervorkian, the practice of mercy killing extends back to Ancient Greece and beyond. In America, the debate has raged for well over a century.
Now, in A Merciful End, Ian Dowbiggin offers the first full-scale historical account of one of the most controversial reform movements in America. Drawing on unprecedented access to the archives of the Euthanasia Society of America, interviews with important figures in the movement today, and flashpoint cases such as the tragic fate of Karen Ann Quinlan, Dowbiggin tells the dramatic story of the men and women who struggled throughout the twentieth century to change the nation's attitude--and its laws--regarding mercy killing. In tracing the history of the euthanasia movement, he documents its intersection with other progressive social causes: women's suffrage, birth control, abortion rights, as well as its uneasy pre-WWII alliance with eugenics. Such links brought euthanasia activists into fierce conflict with Judeo-Christian institutions who worried that "the right to die" might become a "duty to die." Indeed, Dowbiggin argues that by joining a sometimes overzealous quest to maximize human freedom with a desire to "improve" society, the euthanasia movement has been dogged by the fear that mercy killing could be extended to persons with disabilities, handicapped newborns, unconscious geriatric patients, lifelong criminals, and even the poor. Justified or not, such fears have stalled the movement, as more and more Americans now prefer better end-of-life care than wholesale changes in euthanasia laws.
For anyone trying to decide whether euthanasia offers a humane alternative to prolonged suffering or violates the "sanctity of life," A Merciful End provides fascinating and much-needed historical context. -
Whether people have a right to control their own death has become a topic of increasing interest to everyone involved – governments that try to impose their will on individuals, advocates on both sides of the question, and those most directly affected, the terminally ill. This book, inspired by the Compassion in Dying Federation, looks at the issue personally, from the standpoint of the dying and those directly involved in the process. Editor Barbara Coombs Lee highlights stories of individuals and their graceful release into death that can happen when people are given a choice. But there are also powerful accounts by family members, friends, and religious advisers who respected and supported that choice – including those who opted for physician-assisted death. This publication coincides with the 10th anniversary of the Compassion in Dying Federation.
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Recent headlines from Florida involved a brain-damaged woman on life support for more than 13 years. Because there was no written living will, decisions concerning her incapacitation were repeatedly taken to court and even addressed by the governor of the state.
Discusses specifics of a living will, including medical emergencies Contrasts a living will and health care power of attorney Details regulations in all 50 states and the District of Columbia Contains state-specific living will forms Covers cancellation of living will information
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There are few issues more divisive than what has become known as "the right to die." One camp upholds "death with dignity," regarding the terminally ill as autonomous beings capable of forming their own judgment on the timing and process of dying. The other camp advocates "sanctity of life," regarding life as intrinsically valuable, and that should be sustained as long as possible. Is there a right answer? Raphael Cohen-Almagor takes a balanced approach in analyzing this emotionally charged debate, viewing the dispute from public policy and international perspectives. He offers an interdisciplinary, compelling study in medicine, law, religion, and ethics. It is a comprehensive look at the troubling question of whether physician-assisted suicide should be allowed. Cohen-Almagor delineates a distinction between active and passive euthanasia and discusses legal measures that have been invoked in the United States and abroad. He outlines reasons non-blood relatives should be given a role in deciding a patient's last wishes. As he examines euthanasia policies in the Netherlands and the 1994 Oregon Death with Dignity Act, the author suggests amendments and finally makes a circumscribed plea for voluntary physician-assisted suicide.
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Do you own your body? Advances in science and the development of genetic databases have added an aura of modern controversy to this long-standing and, as yet, unresolved problem. In particular, English law governing separated human tissue (including body parts and cell-lines) is unsatisfactory. Despite the enactment of the Human Tissue Act 2004 UK, it remains uncertain what property rights living persons can claim over their separated human tissue. The development of clear legal principles is necessary so that individuals can have effective control over human tissue separated from their bodies whilst also enabling the efficient use of such materials in medical research. Part I of Law and the Human Body traces the evolution of English, Australian, United States and Canadian law in relation to human tissue separated from living persons and dead bodies. This includes a comprehensive examination of the Human Tissue Act 2004 UK as well as prominent judicial decisions, including Re Organ Retention Group Litigation [2005 QB 506, Colavito v New York Organ Donor Network Inc 8 NY 3d 43 (NY CA 2006) and Washington University v Catalona 437 F Supp 2d 985 (USDC Ed Mo 2006). Analysis demonstrates that, although property rights and non-proprietary interests in separated human tissue are recognized in limited circumstances, no principled basis has been accepted either at common law or by statute for the recognition of these rights and interests. Part II of this book therefore develops and defends a principled basis in English law for the creation and legal recognition of property rights and non-proprietary interests in separated human tissue. Significantly, the analysis and principles presented in Law and the Human Body have application across common law and civil law jurisdictions worldwide.
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It won't happen to me.
I'm too busy to worry about a living will.
My family will know what to do.
No one wants to plan for death or incapacitating illness. But, as the emotional legal battle in the Terri Schiavo case made all too clear, people of all ages need to document and communicate clear decisions about the final details of their lives while they are healthy and have time to fully consider their own values and preferences.
Here, Drs. David Doukas and William Reichel help individuals make decisions and communicate their wishes to health care providers and family members and other loved ones.
Drs. Doukas and Reichel use a question-and-answer format to guide readers through the process -- emphasizing the crucial connection between values and treatment preferences. They explain advance directives and the health care decision-making process, including the values history, family covenants, proxies, and proxy negation. The appendix includes resources and Web links for learning about advance directive requirements and obtaining legal forms in all fifty states.
This practical guide helps people navigate the important but often intimidating process of thinking about, and planning for, an uncertain future.
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When her husband was dying from prostate cancer, former Oregon Governor Barbara Roberts had to look inside herself to survive. What she found in that journey fills the pages of this frank but inspiring book. Written for both the patient facing death and those he or she leaves behind, Death Without Denial, Grief Without Apology shows readers how to abandon the silence that too often accompanies these natural processes and find peace within them. Chapter titles include “A Culture in Denial,” “Hospice,” “Permission to Be Weird,” “The Long Slow Climb Back,” and “Reaching Out to Others.”
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Simple forms that protect and save money for you and your family.
Admit it. You have been thinking about getting together all the documents you need to protect yourself and your family should something unexpected happen. But the thought of the time it would take and the amount of work involved has just seemed like too much. Not anymore.
The Easy Will and Living Will Kit provides all the documents you need in one place. In just minutes, you can follow the simple steps it takes to prepare your will, living will and powers of attorney. Begin by choosing the will form that is right for you.
Every form is ready-to-use and modifiable for your needs.
Putting your affairs in order has never been easier. -
Your guide to state law on powers of attorney, right to die, nursing home benefits, wills, trusts, probate, and more.
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Guide to Texas Elder Law for more details visit www.Premack.com
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