360 pp., 6.125 x 9.25, 9 illus. , notes, bibl., index
Studies in Social Medicine
Sickle Cell Anemia and the Politics of Race and Health
2005 William H. Welch Medal, American Association for the History of Medicine
2002 Humanities Honor Book, New Jersey Council for the Humanities
2001 Susanne M. Glasscock Humanities Book Prize for Interdisciplinary Scholarship, Melbern G. Glasscock Center for Humanities Research
2002 Lillian Smith Book Award, Southern Regional Council
2002 Best Book Prize in Race, Ethnicity, and Politics, American Political Science Association
This groundbreaking book chronicles the history of sickle cell anemia in the United States, tracing its transformation from an "invisible" malady to a powerful, yet contested, cultural symbol of African American pain and suffering. 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
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.
"Wailoo's comprehensive telling . . . is the definitive story of race and health in the United States."
"A compelling demonstration of how powerful and significant [the] underappreciated interaction between illness and race has been. . . . This unassuming masterpiece of revelation focuses a new, more precise lens on the intersection of race, illness and politics."
--Publishers Weekly, starred review
"A well-documented, sophisticated study by an important scholar in the field of race and American medicine. . . . This first-rate study of how a disease discourse reflects social relations beautifully demonstrates the significance of the politics of race and health to American history and the contributions that historical analysis can make to contemporary health care debates."
--Journal of American History
"An important contribution to the larger project of documenting the health history of black people in the United States."
--Bulletin of the History of Medicine
"When one finishes the book and reflects back on its contents one realizes just how rich Wailoo's approach to his subject is, how much he has covered, how skillfully he has informed, and how nicely he has used the story of [sickle cell anemia] to tell the stories of race, politics, and health in twentieth-century American society."
"The power of black bodies and their afflictions to 'tell a moral tale' about changing racial relations in US society is bound to fascinate, infuriate and inspire reads of Dying in the City of the Blues . . . . This remarkable text on the social construction of the illness speaks of how ancient, bloody, brutal and enduring the facts of racial disparity in health and care really are in the American experience . . . . What makes this book such an achievement is the author's eye and ear for luminous detail."
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