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They Leave Their Kidneys in the Fields takes the reader on an ethnographic tour of the melon and corn harvesting fields of California’s Central Valley to understand why farmworkers suffer heatstroke and chronic illness at rates higher than workers in any other industry. Through captivating accounts of the daily lives of a core group of farmworkers over nearly a decade, Sarah Bronwen Horton documents in startling detail how a tightly interwoven web of public policies and private interests creates exceptional and needless suffering.
The Affordable Care Act’s impact on coverage, access to care, and systematic exclusion in our health care system The Affordable Care Act set off an unprecedented wave of health insurance enrollment as the most sweeping overhaul of the U.S. health insurance system since 1965. In the years since its enactment, some 20 million uninsured Americans gained access to coverage. And yet, the law remained unpopular and politically vulnerable. While the ACA extended social protections to some groups, its implementation was troubled and the act itself created new forms of exclusion. Access to affordable coverage options were highly segmented by state of residence, income, and citizenship status. Unequal Coverage documents the everyday experiences of individuals and families across the U.S. as they attempted to access coverage and care in the five years following the passage of the ACA.It argues that while the Affordable Care Act succeeded in expanding access to care, it did so unevenly, ultimately also generating inequality and stratification. The volume investigates the outcomes of the ACA in communities throughout the country and provides up-close, intimate portraits of individuals and groups trying to access and provide health care for both the newly insured and those who remain uncovered. The contributors use the ACA as a lens to examine more broadly how social welfare policies in a multiracial and multiethnic democracy purport to be inclusive while simultaneously embracing certain kinds of exclusions. Unequal Coverage concludes with an examination of the Affordable Care Act’s uncertain legacy under the new Presidential administration and considers what the future may hold for the American health care system. The book illustrates lessons learned and reveals how the law became a flashpoint for battles over inequality, fairness, and the role of government. More books on the health care debate
This book is a part of the Ethnographic Studies in Medical Anthropology series.Protecting the health of family members is one of the major responsibilities of women in the Turkish family. Studying women's changing roles from within a rural family, the author presents a complex network of social relations which incorporates both traditional healing methods such as bone-setting and the services of the nationally sponsored health clinic. Following a patient-centered ethnographic approach, the book reveals the community's construction of the “natural” caring of mothers, wives, daughters, and daughters-in-law. Muslim practice and Islamic revivalism; tradition and modernity; global, national and regional identity; and gender shape local concepts of health and illness. For example, a villager who does not believe that microbes cause illness may be flown to relatives in Germany for a surgical operation. Describing the verdant and rugged coast and the everyday life of the spirited individuals who inhabit it, this study examines the metaphors used to describe the body and its suffering — from birth to death — and places a small Black Sea village community in the global context of labor migration, religious trends, and medical technologies.
Working Cures explores black health under slavery showing how herbalism, conjuring, midwifery and other African American healing practices became arts of resistance in the antebellum South and invoked conflicts.
In this chilling history of the bodysnatching trade, the stories of Britain's lesser known Resurrection Men are told. Here are the stories of the men who robbed graves during the winter months of 1742 - 1832, selling fresh cadavers to anatomists up and down the country all in aid of medical advancement. The murders of Burke and Hare often dominate the macabre tales of bodysnatching, but the stories of Henry Gillies, William Patrick and Joseph Grainger are all just as gruesome. Stories involving medical students and anatomists are retold as we discover the cases that have become hidden in history. Anatomy schools, short of fresh cadavers for dissection would pay high prices for corpses, asking no questions about their origins. This resulted in the criminal underworld of the ‘Sack ‘em up Men’ or bodysnatchers, which spread fear and horror throughout the United Kingdom. It’s time to discover these lesser known stories about Britain’s often forgotten history.
Sarah D. Phillips examines the struggles of disabled persons in Ukraine and the other former Soviet states to secure their rights during the tumultuous political, economic, and social reforms of the last two decades. Through participant observation and interviews with disabled Ukrainians across the social spectrum -- rights activists, politicians, students, workers, entrepreneurs, athletes, and others -- Phillips documents the creative strategies used by people on the margins of postsocialist societies to assert claims to "mobile citizenship." She draws on this rich ethnographic material to argue that public storytelling is a powerful means to expand notions of relatedness, kinship, and social responsibility, and which help shape a more tolerant and inclusive society.
When People Come First critically assesses the expanding field of global health. It brings together an international and interdisciplinary group of scholars to address the medical, social, political, and economic dimensions of the global health enterprise through vivid case studies and bold conceptual work. The book demonstrates the crucial role of ethnography as an empirical lantern in global health, arguing for a more comprehensive, people-centered approach. Topics include the limits of technological quick fixes in disease control, the moral economy of global health science, the unexpected effects of massive treatment rollouts in resource-poor contexts, and how right-to-health activism coalesces with the increased influence of the pharmaceutical industry on health care. The contributors explore the altered landscapes left behind after programs scale up, break down, or move on. We learn that disease is really never just one thing, technology delivery does not equate with care, and biology and technology interact in ways we cannot always predict. The most effective solutions may well be found in people themselves, who consistently exceed the projections of experts and the medical-scientific, political, and humanitarian frameworks in which they are cast. When People Come First sets a new research agenda in global health and social theory and challenges us to rethink the relationships between care, rights, health, and economic futures.

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