Men and women who have done the hardest thing of all--lived lives of virtue so heroically that their deeds will be honored as long as there's Church. Let these superheoes and superheroines show you how exciting a life of Faith can be.
Bioethics emerged at a time when infectious diseases were not a major concern. Thus bioethics never had to develop a normative framework sensitive to situations of disease transmission. The Patient as Victim and Vector explores how traditional and new issues in clinical medicine, research, public health, and health policy might look different in infectious disease were treated as central. The authors argue that both practice and policy must recognize that a patient with a communicable infectious disease is not only a victim of that disease, but also a potential vector- someone who may transmit an illness that will sicken or kill others. Bioethics has failed to see one part of this duality, they document, and public health the other: that the patient is both victim and vector at one and the same time. The Patient as Victim and Vector is jointly written by four authors at the University of Utah with expertise in bioethics, health law, and both clinical practice and public health policy concerning infectious disease. Part I shows how the patient-centered ethic that was developed by bioethics- especially the concept of autonomy- needs to change in the context of public health, and Part II develops a normative theory for doing so. Part III examines traditional and new issues involving infectious disease: the ethics of quarantine and isolation, research, disease screening, rapid testing, antibiotic use, and immunization, in contexts like multi-drug-resistant tuberculosis, syphilis, hepatitis, HIV/AIDS, and HPV. Part IV, beginning with a controversial thought experiment, considers constraint in the control of infectious disease, include pandemics, and Part V 'thinks big' about the global scope of infectious disease and efforts to prevent, treat, or eradicate it. This volume should have a major impact in the fields of bioethics and public health ethics. It will also interest philosophers, lawyers, health law experts, physicians, and policy makers, as well as those concerned with global health.
Notes at the end of each book Vatican II Constitution on Divine Revelation Presentation page Family record page Land of the Bible in full color Gift box 1,556 pp.
This biography of an early twentieth-century South Carolina doctor sheds light on his pioneering work with the mentally ill to combat a public health scourge. Thousands of Americans died of pellagra before the cause—vitamin B3 deficiency—was identified. Credit for solving the mystery is usually given to Dr. Joseph Goldberger of the US Public Health Service. But in Asylum Doctor, Charles S. Bryan demonstrates that a coalition of American asylum superintendents, local health officials, and practicing physicians set the stage for Golberger’s historic work—chief among them was Dr. James Woods Babcock. As superintendent of the South Carolina State Hospital for the Insane from 1891 to 1914, Babcock sounded the alarm against pellagra. He brough out the first English-language treatise on the subject and organized the National Association for the Study of Pellagra. He did so in the face of troubled asylum governance which, coupled with Governor Cole Blease’s political intimidation and unblushing racism, eventually drove Babcock from his post. Asylum Doctor describes the plight of the mentally ill in South Carolina during an era when public asylums had devolved into convenient places to warehouse inconvenient people. It is the story of an idealistic humanitarian who faced conditions most people would find intolerable. And it is important social history for, as this book’s epigraph puts it, “in many ways the Old South died with the passing of pellagra.”
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