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Available From UC Press
Health Care Off the Books
Millions of low-income African Americans in the United States lack access to health care. How do they treat their health care problems? In Health Care Off the Books, Danielle T. Raudenbush provides an answer that challenges public perceptions and prior scholarly work. Informed by three and a half years of fieldwork in a public housing development, Raudenbush shows how residents who face obstacles to health care gain access to pharmaceutical drugs, medical equipment, physician reference manuals, and insurance cards by mobilizing social networks that include not only their neighbors but also local physicians. However, membership in these social networks is not universal, and some residents are forced to turn to a robust street market to obtain medicine. For others, health problems simply go untreated.
Raudenbush reconceptualizes U.S. health care as a formal-informal hybrid system and explains why many residents who do have access to health services also turn to informal strategies to treat their health problems. While the practices described in the book may at times be beneficial to people’s health, they also have the potential to do serious harm. By understanding this hybrid system, we can evaluate its effects and gain new insight into the sources of social and racial disparities in health outcomes.
"Raudenbush breaks new ground by showing how low-income people, locked out of the formal health care system, are forced to turn to a shadow health care network for basic medical necessities. This gripping and beautifully written book is a must-read for anyone interested in poverty, health care, and the connections between them."—Judith A. Levine, author of Ain’t No Trust: How Bosses, Boyfriends, and Bureaucrats Fail Low-Income Mothers and Why It Matters
“Health Care Off the Books demonstrates how the creative strategies that people leverage to address a lack of resources, while perhaps helpful in the short run, can be deadly in the long run. This book is a scathing indictment of our refusal to see access to high-quality health care as a human right. It should be required reading for those interested in understanding the context and consequences of injuries of inequality.”—Celeste Watkins-Hayes, Professor of Sociology and African American Studies at Northwestern University and author of Remaking a Life: How Women Living with HIV/AIDS Confront Inequality