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Set in Memphis, home of one of the nation's first sickle cell clinics, Dying in the City of the Blues reveals how the recognition, treatment, social understanding, and symbolism of the disease evolved in the twentieth century, shaped by the politics of race, region, health care, and biomedicine. Using medical journals, patients' accounts, black newspapers, blues lyrics, and many other sources, Keith Wailoo follows the disease and its sufferers from the early days of obscurity before sickle cell's "discovery" by Western medicine; through its rise to clinical, scientific, and social prominence in the 1950s; to its politicization in the 1970s and 1980s. Looking forward, he considers the consequences of managed care on the politics of disease in the twenty-first century.
A rich and multilayered narrative, Dying in the City of the Blues offers valuable new insight into the African American experience, the impact of race relations and ideologies on health care, and the politics of science, medicine, and disease.
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A simple introduction to sickle cell anemia, describing its symptoms, its effects on the body, and how to cope with this disease.
Sickle Cell Anemia: A Mother's Perspective offers information that every parent should know when caring for a child diagnosed with this disease. The goal of this book is to share a firsthand ...
This is a reproduction of a book published before 1923. This book may have occasional imperfections such as missing or blurred pages, poor pictures, errant marks, etc. that were either part of the ...
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For anyone who has or is predisposed to sickle cell disease, this informative and compassionate guide provides all the facts patients, loved ones, and caregivers need to know in order to reduce ...
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