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"The book is extremely well balanced: in each section there is usually an argument for and against the positions raised. It is a useful and well-thought-out text. It will make people think and discuss the problems raised, which I think is the editor's main purpose." -- Journal of Medical Ethics "... a volume that is to be commended for the clarity of its contributions, and for the depth it gains from its narrow focus. In places, this is a deeply moving, as well as closely argued, book." -- Times Literary Supplement "This work is an excellent historical and philosophical resource on a very difficult subject." -- Choice "This collection of well-written and carefully argued essays should be int...
This book will show the richness and diversity of death as a subject in a variety of literary genres. Second, it will demonstrate the timelessness of the subject of death in literature, as evidence by selections ranging from 2300 B.C. to A.D. 1979. Third, it will reflect a variety of cultural traditions through selections from India, China, Japan, Greece, Nigeria, Lebanon, Russia, Germany, England, France, Spain, Ireland, and the United States. Fourth, it will be a helpful book for teaching courses on death in the humanities and a beneficial book for all persons who want to enrich their lives by sensitizing themselves to the mortality shared by us all.
For Bioethicists and their students; physicians; philosophers; all those concerned with death and dying in a clinical setting. This book offers an in-depth analysis of 'passive euthanasia' - the process involved in 'allowing to die' decisions. The author develops a new conceptual model for this issue, provides an insightful historical overview, discusses clinical settings in which abating treatment takes place, and interprets relevant legal documents pertaining to the right to refuse life-sustaining treatment. After interpreting widely disparate ethical positions, he develops his own comprehensive ethical theory, one that is medically realistic, philosophically sound, and legally viable.
Contains the papers of various members of the Weir family, including Robert Walter Weir (1803-1889), John F. Weir (1841-1926), and Julian Alden Weir (1852-1919) and others. Contains correspondence, diaries, scrapbooks, manuscripts, speeches, artwork, clippings, and published material relating to the family, dating from between 1765 to 1952. The bulk of the collection relates to Julian Alden Weir.
Genetics research with stored human tissues provides many benefits and holds much promise. Yet how this critical research is conducted sometimes raises serious ethical, legal, and social concerns, and it is difficult to balance the promise of biomedical research with our time-honored commitments to individual choice in such fundamental matters as control over personal health information and the disposition of our bodily tissues. Weir and Olick provide a thorough analysis of this critical phase in the era of genomic medicine. While strongly supportive of the biomedical research enterprise, they develop a critique of many common research practices with banked tissues, DNA, and genetic data. No...
Who decides, and on what basis, how to treat a child with severe birth defects? Any decisions made on such cases are painful and complex, and have far-reaching consequences for society at large. Addressing the medical, legal, and ethical aspects of the issue, Robert Weir presents the first serious survey of the major arguments regarding selective non-treatment, which have been advanced by physicians, attorneys, and the judicial system.
"Title of papers, addresses, &c., from 1807 to 1874": 1875 p. 94-111.
Progress in biomedical science has called for an international discussion of the medical, ethical, and legal problems that confront physicians, medical researchers, infertile couples, pregnant women, and parents of premature or disabled infants. In addition, the unprecedented technological developments in obstetrical, perinatal, and neonatal medicine in recent years have indicated a need for an international forum for interdisciplinary dialogue regarding the definition of early human life, the neurological development of early human life, the value of early human life, the obligations for its protection and prolongation, and the limits to these obligations.