"This book will be an important resource for physicians, medical ethicists, and other health care professionals as they deal with the rights and prerogatives of the dying and the legal and policy questions surrounding the choices to be made in the conduct of their care." -- New Jersey Medicine "Disquieted that the wishes of dying patients do not direct care at the end of life even when their intentions and plans have been put to writing in an advance directive, Olick rethinks and reinvigorates the case for patient and family control in the face of significant challenges to the nature, scope, and importance of autonomy in the care of incompetent dying patients." -- Book News, Inc. "I recommend this book highly to all health care professionals. It is clearly written, and beautifully argued. It was a pleasure to read such lucid prose reflecting clear thinking. It certainly gave a me a different perspective from which to argue for the rights of patients to die in a dignified manner, a topic that is important to all of us, health care professional or not." -- Nursing Ethics "The book is simultaneously a model of scholarship and a work of advocacy that if heeded would dramatically change the way many patients die. Highly recommended for upper-division undergraduate and graduate students and faculty, and essential reading for professionals and practitioners." -- Choice "An important resource for health-care professionals, medical ethicists, and legal scholars who are involved in the legal rights and policy issues surrounding end-of-life decisions." -- Medical Humanities Review
