The Troubled Dream Of Life

Drawing on his own experience, and on literature, philosophy, and medicine, Daniel Callahan offers great insight into how to deal with the rewards of modern medicine without upsetting our perception of death. He examines how we view death and the care of the critically ill or dying, and he suggests ways of understanding death that can lead to a peaceful acceptance. Callahan's thoughtful perspective notably enhances the legal and moral discussions about end-of-life issues. Originally published in 1993 by Simon and Schuster.

Drawing on his own experience and on literature, philosophy, and medicine, Callahan offers profound insight on how to deal with the rewards of modern medicine without upsetting our equilibrium and perspective on death and dying. "A profound essay on what it means to die in a world shaped by medical technology".--The Washington Times.

Winner of the History of Science category of the Professional and Scholarly Publishing Awards given by the Association of American Publishers Why do racial and ethnic controversies become attached, as they often do, to discussions of modern genetics? How do theories about genetic difference become entangled with political debates about cultural and group differences in America? Such issues are a conspicuous part of the histories of three hereditary diseases: Tay-Sachs, commonly identified with Jewish Americans; cystic fibrosis, often labeled a "Caucasian" disease; and sickle cell disease, widely associated with African Americans. In this captivating account, historians Keith Wailoo and Stephen Pemberton reveal how these diseases—fraught with ethnic and racial meanings for many Americans—became objects of biological fascination and crucibles of social debate. Peering behind the headlines of breakthrough treatments and coming cures, they tell a complex story: about different kinds of suffering and faith, about unequal access to the promises and perils of modern medicine, and about how Americans consume innovation and how they come to believe in, or resist, the notion of imminent medical breakthroughs. With Tay-Sachs, cystic fibrosis, and sickle cell disease as a powerful backdrop, the authors provide a glimpse into a diverse America where racial ideologies, cultural politics, and conflicting beliefs about the power of genetics shape disparate health care expectations and experiences.

William F. May, a leading expert on medical ethics, here explores two of today's most crucial tests of the medical covenant - active euthanasia and health care reform.May begins with an incisive introduction that delineates the covenantal, or relational, nature of the practice of medicine over against the merely contractual view - the quid pro quos of the commercial buying and selling of professional services. In the subsequent chapters, May follows the implications of the medical covenant with respect to the related issues of euthanasia and health care reform. He also provides a covenantal view of professional character and virtue - what virtues we should look for in covenanted physicians and nurses - discusses the limits of the medical covenant in the face of medical futility, and examines the implications of covenant keeping for the shape of future health care reform.

Theo and her young, irresponsible mother seem trapped forever in their miserable, poverty-stricken life … but Theo can’t stop dreaming of belonging to a “real” family. When she is mysteriously adopted by the large, warm Kaldor family, her dream seems to be coming true. But as time passes, the magic of Theo’s new life begins to fade, and soon she finds herself back with her mother. Were the Kaldors real or just a dream? Who is the shadowy figure who haunts Theo’s thoughts? And, most importantly, will Theo ever be able to find a real home with a family she can truly call her own?