Dying in the City of the Blues

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.<br/><br/>Set in Memphis home of one of the nation’s first sickle cell clinics <i>Dying in the City of the Blues</i> 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.<br/><br/>A rich and multilayered narrative <i>Dying in the City of the Blues</i> 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.