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OverviewA moving cultural history of disability—and a powerful call to action to change how our medical system and society supports those with complex chronic conditions From lupus to Lyme, invisible illness is often dismissed by everyone but the sufferers. Why does the medical establishment continually insist that, when symptoms are hard to explain, they are probably just in your head? Inspired by her work with long Covid patients, medical anthropologist Emily Mendenhall traces the story of complex chronic conditions from hysteria to long Covid to show why both research and practice fail so many. Mendenhall points out disconnects between the reality of chronic disease—which typically involves multiple intersecting problems resulting in unique, individualized illness—and the assumptions of medical providers, who behave as though illnesses have uniform effects for everyone. And while invisible illnesses have historically been associated with white middle-class women, being believed that you are sick is even more difficult when you're Black, trans, poor, young, disabled, or undocumented. Weaving together cultural history with intimate interviews, Invisible Illness lifts up the experiences of those living with complex illness to expose the failures of the American healthcare system—and how we can do better. Full Product DetailsAuthor: Emily MendenhallPublisher: University of California Press Imprint: University of California Press ISBN: 9780520421523ISBN 10: 0520421523 Pages: 264 Publication Date: 06 January 2026 Audience: Professional and scholarly , College/higher education , Professional & Vocational , Postgraduate, Research & Scholarly Format: Hardback Publisher's Status: Active Availability: Out of stock The supplier is temporarily out of stock of this item. It will be ordered for you on backorder and shipped when it becomes available. Table of ContentsContents A Note on Names A Glossary of Conditions Introduction PART ONE: HISTORY 1. Hysteria Is an Old Story 2. The Case of Chronic Fatigue 3. Lyme Wars 4. Pain without Verifiability PART TWO: POLITICS 5. Disabling Culture 6. The Rise of Patient Activism 7. Structural Silencing 8. Disability Consciousness Conclusion Acknowledgments Notes Bibliography IndexReviews“Elegantly written and rigorously researched . . . An incisive study that illuminates the myriad complexities of chronic illness.” * Kirkus Reviews, starred review * “Elegantly written and rigorously researched . . . An incisive study that illuminates the myriad complexities of chronic illness.” * Kirkus Reviews, starred review * ""Movingly spotlights the struggles of chronically ill patients who experience maddening dismissals by their own doctors. An urgent argument for updating standards of care and a hopeful look at how long Covid could prompt a major medical turning point."" * Publishers Weekly * Author InformationEmily Mendenhall is Professor in the Walsh School of Foreign Service at Georgetown University, a Guggenheim Fellow, and contributor to Scientific American, Psychology Today, and Vox. Tab Content 6Author Website:Countries AvailableAll regions |
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