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Blood Sagaby Susan Resnik
Synopses & Reviews
For thousands of years boys known as "bleeders" faced an early, painful death from hemophilia. Dubbed "the Royal Disease" because of its identification with Queen Victoria, the world's most renowned carrier, hemophilia is a genetic disease whose sufferers had little recourse until the mid-twentieth century. In the first book to chronicle the emergence and transformation of the hemophilia community, Susan Resnik sets her story within our national political landscape—where the disease is also a social, psychological, and economic experience.
Blood Saga includes many players and domains: men with hemophilia and their families, medical personnel, science researchers, and the author herself, who was Director of Education of the National Hemophilia Foundation in the early 1980s. At that time the "miracle treatment" of freeze-dried pooled plasma blood products enabled men with hemophilia to lead full, normal lives. Then the AIDS virus infiltrated the treatment system and over fifty percent of the hemophilia community became HIV-positive. But rather than collapsing, this community refocused its priorities, extended its reach, and helped shape blood safety policies to prevent further tragedy.
The hemophilia community includes people from every socioeconomic and ethnic group, and Resnik's narrative and use of oral histories never lose touch with those affected by the disease. Her extensive informant interviewing allows much of this social history to be told by participants on all levels: parents, wives, nurses, doctors, government agency directors, health care providers, and many others.
Gene insertion therapy now holds the promise of a cure for hemophilia in the near future. Scientific breakthroughs inevitably become intertwined with the industry and academic medical centers that govern the national health care system. And in that system, says Resnik, costs and safety are sometimes contending issues. She makes clear that the lessons learned in Blood Saga apply to all of us.
The social history of hemophilia in the United States, focusing on the patients and their families who fought to participate in the study and treatment of their disease and who advocated for blood safety in the face of AIDS.
"A beautifully wrought book that is an important addition to the social history of medicine. It is a compassionate and highly readable account of a part of the medical picture that is too often ignored—the patients."—Douglas Starr, author of Blood: An Epic History of Medicine and Commerce
"Susan Resnik has interpreted the engrossing story of hemophilia to engage both the sophisticated scientist and the curious general reader. She raises important ethical issues and helps translate words into actions, turning information into real change."—Clarence E. Pearson, President, National Center for Health Education
"The struggles of the hemophilia community are artfully described as the author traces the journey of hemophilia from ignorance and caricature to a growing international awareness of the need for health education, quality control over therapies, and the application of the ethical standards of our public health community in the treatment of hemophiliac persons."—Audrey R. Gotsch, President, American Public Health Association
About the Author
Susan Resnik teaches at the University of California, San Diego, Medical School, and was formerly Director of Education of the National Hemophilia Foundation. She lives in Del Mar, California.
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