{"title":"Studies In Social Medicine","description":"\u003cp\u003eDelve into the complex interplay of society and health with the Studies in Social Medicine series. Explore key research and perspectives shaping our understanding of well-being and healthcare policies.\u003c\/p\u003e","products":[{"product_id":"prozac-as-a-way-of-life-book-tod-chambers-9780807828809","title":"Prozac As a Way of Life","description":"Prozac and its chemical cousins, Paxil, Celexa, and Zoloft, are some of the most profitable and most widely used drugs in America. Their use in the treatment of a multitude of disorders - from generalized anxiety disorder and premenstrual syndrome to eating disorders and sexual compulsions - has provoked a whirlwind of public debate. Talk shows ask, Why is Prozac so popular? What, exactly, do these drugs treat? But sustained critical discussion among bioethicists and medical humanists has been surprisingly absent. The eleven essays in Prozac as a Way of Life provide the groundwork for a much-needed philosophical discussion of the ethical and cultural dimensions of the popularity of SSRI antidepressants. Focusing on the increasing use of medication as a means of self-enhancement, contributors from the fields of psychiatry, psychology, bioethics, and the medical humanities address issues of identity enhancement, the elasticity of psychiatric diagnosis, and the aggressive marketing campaigns of pharmaceutical companies. They do not question the fact that these antidepressants can, in some cases, provide great benefit to alleviate real suffering. 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Abel offers the first history of fatigue, one that is scrupulously researched but also informed by her own experiences as a cancer survivor. Abel reveals how the limits of medicine and the American cultural emphasis on productivity intersect to stigmatize those with fatigue. Without an agreed-upon approach to confirm the problem through medical diagnosis, it is difficult to convince others that it is real. When fatigue limits our ability to work, our society sees us as burdens or worse.   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With a compassionate look at the individual decision making behind the desire to become pregnant and the use of assisted reproductive technologies (ART), Harwood extends the public conversation beyond debates about individual choice by considering the experiences of families and by addressing the broader ethical problems presented by these technologies. Incorporating the personal narratives of women who are members of RESOLVE, the nation's leading organization for people who are infertile, Harwood demonstrates that repeated unsuccessful attempts to use ART may ironically help women come to terms with their infertility. Yet ART is problematic for a number of reasons, including the financial, physical, and emotional costs for women and their families as well as the effects of these technologies on the health and well-being of the children conceived. Issues such as consumerism, workplace norms that encourage delayed childbearing, and narrow definitions of family all come into play. 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Highlighting the rise of Parents Anonymous and connecting their activism to the sexual abuse moral panic that swept the country in the 1980s, Raz argues that these panics and policies?as well as biased viewpoints regarding race, class, and gender?played a powerful role shaping perceptions of child abuse. 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Since 1990, immigration to the United States has risen sharply, and rural areas have seen the highest increases. Thurka Sangaramoorthy reveals that that the corporatization of health care delivery and immigration policies are deeply connected in rural America. Drawing from fieldwork that centers on Maryland's sparsely populated Eastern Shore, Sangaramoorthy shows how longstanding issues of precarity among rural health systems along with the exclusionary logics of immigration have mutually fashioned a landscape of care in which shared conditions of physical suffering and emotional anxiety among immigrants and rural residents generate powerful forms of regional vitality and social inclusion. Sangaramoorthy connects the Eastern Shore and its immigrant populations to many other places around the world that are struggling with the challenges of global migration, rural precarity, and health governance. Her extensive ethnographic and policy research shows the personal stories behind health inequity data and helps to give readers a human entry point into the enormous challenges of immigration and rural health.","brand":"WoB","offers":[{"title":"US \/ VERY_GOOD \/ SBYB","offer_id":49888015745297,"sku":"CIN1469674173VG","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"GB \/ NEW \/ GARDNERS","offer_id":50630817382673,"sku":"NGR9781469674162","price":0.0,"currency_code":"GBP","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0784\/4072\/6801\/files\/1469674165.jpg?v=1763479317"},{"product_id":"dying-in-the-city-of-the-blues-book-keith-wailoo-9780807848968","title":"Dying in the City of the Blues","description":"Understanding the connections between culture, race, politics, and disease 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, where one of the nation's first sickle cell clinics was founded in the 1950s, 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.","brand":"WoB","offers":[{"title":"US \/ GOOD \/ SBYB","offer_id":49950951244049,"sku":"CIN0807848964G","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"US \/ NEW \/ INGRAM","offer_id":51007753322769,"sku":"NIN9780807848968","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"US \/ VERY_GOOD \/ SBYB","offer_id":51416418812177,"sku":"CIN0807848964VG","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"GB \/ NEW \/ INGRAM","offer_id":52406794715409,"sku":"NLS9780807848968","price":0.0,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0784\/4072\/6801\/files\/0807848964.jpg?v=1752959329"},{"product_id":"remaking-the-american-patient-book-nancy-tomes-9781469622774","title":"Remaking the American Patient","description":"In a work that spans the twentieth century, Nancy Tomes questions the popular - and largely unexamined - idea that in order to get good health care, people must learn to shop for it. 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Told they were being treated for \"\"bad blood,\"\" the nearly four hundred men with late-stage syphilis and two hundred disease-free men who served as controls were kept away from appropriate treatment and plied instead with placebos, nursing visits, and the promise of decent burials. Despite the publication of more than a dozen reports in respected medical and public health journals, the study continued for forty years, until extensive media coverage finally brought the experiment to wider public knowledge and forced its end. This edited volume gathers articles, contemporary newspaper accounts, selections from reports and letters, reconsiderations of the study by many of its principal actors, and works of fiction, drama, and poetry to tell the Tuskegee story as never before. Together, these pieces illuminate the ethical issues at play from a remarkable breadth of perspectives and offer an unparalleled look at how the study has been understood over time. |This book uniquely reveals the history and legacy of the infamous Tuskegee syphilis study through a comprehensive collection of documents: articles, reports, letters, and newspaper accounts, as well as works of fiction, poetry, and drama.","brand":"WoB","offers":[{"title":"US \/ GOOD \/ SBYB","offer_id":50100342522129,"sku":"CIN0807848522G","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"US \/ NEW \/ INGRAM","offer_id":51007837372689,"sku":"NIN9780807848524","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"US \/ VERY_GOOD \/ SBYB","offer_id":51326311760145,"sku":"CIN0807848522VG","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"GB \/ NEW \/ INGRAM","offer_id":52407214080273,"sku":"NLS9780807848524","price":0.0,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0784\/4072\/6801\/files\/0807848522.jpg?v=1763472438"},{"product_id":"death-retold-book-peter-guarnaccia-9780807857731","title":"A Death Retold","description":"In February 2003, an undocumented immigrant teen from Mexico lay dying in a prominent American hospital due to a stunning medical oversight - she had received a heart-lung transplantation of the wrong blood type. In the following weeks, Jesica Santillan's tragedy became a portal into the complexities of American medicine, prompting contentious debate about new patterns and old problems in immigration, the hidden epidemic of medical error, the lines separating transplant \"\"haves\"\" from \"\"have-nots,\"\" the right to sue, and the challenges posed by \"\"foreigners\"\" crossing borders for medical care. This volume draws together experts in history, sociology, medical ethics, communication and immigration studies, transplant surgery, anthropology, and health law to understand the dramatic events, the major players, and the core issues at stake. Contributors view the Santillan story as a morality tale: about the conflicting values underpinning American health care; about the politics of transplant medicine; about how a nation debates deservedness, justice, and second chances; and about the global dilemmas of medical tourism and citizenship.","brand":"WoB","offers":[{"title":"US \/ VERY_GOOD \/ SBYB","offer_id":50167767630097,"sku":"CIN0807857734VG","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"US \/ GOOD \/ SBYB","offer_id":52326433063185,"sku":"CIN0807857734G","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"GB \/ NEW \/ INGRAM","offer_id":52614174998801,"sku":"NLS9780807857731","price":0.0,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0784\/4072\/6801\/files\/0807857734.jpg?v=1752929314"},{"product_id":"infectious-fear-book-samuel-kelton-roberts-jr-9780807859346","title":"Infectious Fear","description":"This title uncovers the links between race, class, and health. For most of the first half of the twentieth century, tuberculosis ranked among the top three causes of mortality among urban African Americans. Often afflicting an entire family or large segments of a neighborhood, the plague of TB was as mysterious as it was fatal. Samuel Kelton Roberts Jr. examines how individuals and institutions - black and white, public and private - responded to the challenges of tuberculosis in a segregated society. Reactionary white politicians and health officials promoted 'racial hygiene' and sought to control TB through Jim Crow quarantines, Roberts explains.African Americans, in turn, protested the segregated, overcrowded housing that was the true root of the tuberculosis problem. Moderate white and black political leadership reconfigured definitions of health and citizenship, extending some rights while constraining others. Meanwhile, those who suffered with the disease - as its victims or as family and neighbors - made the daily adjustments required by the devastating effects of the 'white plague'. Exploring the politics of race, reform, and public health, \"\"Infectious Fear\"\" uses the tuberculosis crisis to reveal the limits of racialized medicine and the roots of modern health disparities. 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Stowe provides an in-depth study of the midcentury culture of everyday medicine in the South. Reading deeply in the personal letters, day-books, diaries, bedside notes, and published writings of doctors, Stowe illuminates an entire world of sickness and remedy, suffering and hope, and the deep ties between medicine and regional culture. In a distinct American region where climate, race and slavery, and assumptions about \"\"southernness\"\" profoundly shaped illness and healing in the lives of ordinary people, Stowe argues that southern doctors inhabited a world of skills, medicines, and ideas about sickness that allowed them to play moral, as well as practical, roles in their communities. Looking closely at medical education, bedside encounters, and medicine's larger social aims, he describes a \"\"country orthodoxy\"\" of local, social medical practice that highly valued the \"\"art\"\" of medicine. While not modern in the sense of laboratory science a century later, this country orthodoxy was in its own way modern, Stowe argues, providing a style of caregiving deeply rooted in individual experience, moral values, and a consciousness of place and time.","brand":"WoB","offers":[{"title":"US \/ GOOD \/ SBYB","offer_id":50307017769233,"sku":"CIN0807828858G","price":0.0,"currency_code":"GBP","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0784\/4072\/6801\/files\/0807828858.jpg?v=1750702918"},{"product_id":"pharmacopolitics-book-arthur-a-daemmrich-9780807828441","title":"Pharmacopolitics","description":"Advocates of rapid access to medicines and critics fearful of inadequate testing both argue that globalization will supersede national medical practices and result in the easy transfer of pharmaceuticals around the world. In Pharmacopolitics, Arthur Daemmrich challenges their assumptions by comparing drug laws, clinical trials, and systems for monitoring adverse reactions in the United States and Germany, two countries with similarly advanced systems for medical research, testing, and patient care. Daemmrich proposes that divergent \"therapeutic cultures\" - the interrelationships among governments, patients, the medical profession, and the pharmaceutical industry - underlie national differences and explain variations in pharmaceutical markets and medical care. Daemmrich carries the United States-Germany comparison from 1950 to the present through case studies of Terramycin (an antibiotic), thalidomide (a sedative), propranolol (a heart medication), interleukin-2 (a cancer therapy), and indinavir (an AIDS drug). He points to important differences in government policies and in the distribution of power among key social actors. 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Some medical men claimed that women were naturally weak, that education would make them physically ill, and that women physicians endangered the profession. Mary Putnam Jacobi (1842-1906), a physician from New York, worked to prove them wrong and argued that social restrictions, not biology, threatened female health.\"\"Mary Putnam Jacobi and the Politics of Medicine in Nineteenth-Century America\"\" is the first full-length biography of Jacobi, the most significant woman physician of her era and an outspoken advocate for women's rights. Jacobi rose to national prominence in the 1870s and went on to practice medicine, teach, and conduct research for over three decades. She campaigned for co-education, professional opportunities, labor reform, and suffrage - the most important women's rights issues of her day. Downplaying gender differences, she used the laboratory to prove that women were biologically capable of working, learning, and voting. 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Focusing on the Kalaupapa Settlement in Moloka'i and the U.S. National Leprosarium in Carville, Michelle Moran shows not only how public health policy emerged as a tool of empire in America's colonies, but also how imperial ideologies and racial attitudes shaped practices at home. Although medical personnel at both sites considered leprosy a colonial disease requiring strict isolation, Moran demonstrates that they adapted regulations developed at one site for use at the other by changing rules to conform to ideas of how \"\"natives\"\" and \"\"Americans\"\" should be treated. By analyzing administrators' decisions, physicians' treatments, and patients' protests, Moran examines the roles that gender, race, ethnicity, and sexuality played in shaping both public opinion and health policy. \"\"Colonizing Leprosy\"\" makes an important contribution to an understanding of how imperial imperatives, public health practices, and patient activism informed debates over the constitution and health of American bodies.","brand":"WoB","offers":[{"title":"US \/ GOOD \/ SBYB","offer_id":50366430576913,"sku":"CIN0807858390G","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"GB \/ NEW \/ INGRAM","offer_id":52654645969169,"sku":"NLS9780807858394","price":0.0,"currency_code":"GBP","in_stock":true},{"title":"US \/ NEW \/ INGRAM","offer_id":52858333135121,"sku":"NIN9780807858394","price":0.0,"currency_code":"GBP","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0784\/4072\/6801\/files\/0807858390.jpg?v=1752987581"},{"product_id":"aids-pandemic-book-lawrence-o-gostin-9780807828304","title":"The AIDS Pandemic","description":"In this collection of essays, Lawrence O. Gostin, a scholar of AIDS law and policy, confronts the most pressing and controversial issues surrounding AIDS in America and around the world. He shows how HIV\/AIDS affects the entire US population - infected and uninfected - by influencing its social norms, economy, and the country's role as a world leader. The nation and the world still fail to respond to the needs of people living with HIV\/AIDS and continue to tolerate injustice in their treatment, Gostin argues. AIDS, both in the USA and globally, deeply affects poor and marginalized populations, and many US policies are based on conservative moral values rather than public health and social justice concerns. Gostin tackles the hard social, legal, political and ethical issues of the HIV\/AIDS pandemic: privacy and discrimination, travel and immigration, clinical trials and drug pricing, exclusion of HIV-infected health-care workers, testing and treatment of pregnant women and infants, and needle-exchange programmes. 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At a time when most women physicians laid claim to \"\"female\"\" qualities of care and nurturance to justify their professional choice, Zakrzewska insisted that all physicians, regardless of gender, should depend upon the rational faculties developed through training in the natural sciences. She viewed science as a democratizing tool - anyone could master science, she asserted, and therefore the doors to the elite profession of medicine should be opened to all. 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But as Chris Feudtner demonstrates, the subsequent transformation of the disease from a fatal condition into a chronic illness is a story of success tinged with irony, a revealing saga that illuminates the complex human consequences of medical intervention.   Bittersweet chronicles this history of diabetes through the compelling perspectives of people who lived with this disease. Drawing on a remarkable body of letters exchanged between patients or their parents and Dr. Elliot P. Joslin and the staff of physicians at his famed Boston clinic, Feudtner examines the experience of living with diabetes across the twentieth century, highlighting changes in treatment and their profound effects on patients' lives. Although focused on juvenile-onset, or Type 1, diabetes, the themes explored in Bittersweet have implications for our understanding of adult-onset, or Type 2, diabetes, as well as a host of other diseases that, thanks to drugs or medical advances, are being transformed from acute to chronic conditions. 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The twelve original essays inthis volume show that common public debates routinely bypass complexethical, sociocultural, historical, and political questions about how we shouldaddress ideals of justice and equality in health care. Integrating perspectivesfrom the humanities, social sciences, medicine, and public health, the contributorsilluminate the relationships between justice and health inequalitiesto complicate and enrich debates often dominated by simplistic narratives.  Understanding Health Inequalities and Justice grounds key conceptualdiscussions in timely case studies and policy analyses that explore threeoverarching questions: first, how do scholars approach relations betweenhealth inequalities and ideals of justice; second, when do justice considerationsinform solutions to health inequalities, and how do specific healthinequalities affect perceptions of injustice; and third, how can diverse scholarlyapproaches contribute to better health policy? From addressing patientagency in an inequitable health care environment to examining how scholarsof social justice and health care amass evidence, this volume combines theskills and sensibilities of diverse scholars to promote a richer understandingof health and justice and the successful paths to their realization.  The contributors are Judith C. Barker, Paula Braveman, Paul Brodwin,Jami Suki Chang, Debra DeBruin, Leslie A. Dubbin, Sarah Horton, Carla C.Keirns, J. Paul Kelleher, Nicholas B. King, Eva Feder Kittay, Joan Liaschenko,Anne Drapkin Lyerly, Mary Faith Marshall, Carolyn Mokley Rouse, JenniferPrah Ruger, and Janet K. 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Examining medical ideas about operations (including cesarean section, abortion, hysterectomy, and eugenic sterilization), Catholic theology, and notions of modernity and identity, O'Brien argues that present-day claims about fetal personhood are rooted in the use of surgical force against marginalized and racialized women. This history illuminates the theological, patriarchal, and epistemological roots of obstetric violence and racism today.  O'Brien illustrates how ideas about maternal worth and unborn life developed in tandem. Eighteenth-century priests sought to save unborn souls through cesarean section, while nineteenth-century doctors aimed to salvage some unmarried women's social reputations via therapeutic abortion. By the twentieth century, eugenicists wished to regenerate the nation's racial profile, in part by sterilizing women in public clinics. 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Both societies have faced rising rates of diabetes, but their social and biomedical responses to its ascendance have diverged. To explain the emergence of distinctive strategies to explain and manage diabetes, Armstrong-Hough argues that physicians act on not only increasingly globalized professional standards but also on local knowledge, explanatory models, and cultural toolkits. As a result, strategies for clinical management diverge sharply from one country to another. Armstrong-Hough demonstrates how distinctive practices endure in the midst of intensifying biomedicalization, both on the part of patients and on the part of physicians, and how these differences grow from broader cultural narratives about diabetes in each setting.","brand":"WoB","offers":[{"title":"- \/ - \/ -","offer_id":50537837429009,"sku":"","price":0.0,"currency_code":"GBP","in_stock":true},{"title":"GB \/ NEW \/ GARDNERS","offer_id":50537837723921,"sku":"NGR9781469646688","price":0.0,"currency_code":"GBP","in_stock":true},{"title":"GB \/ NEW \/ INGRAM","offer_id":52619214815505,"sku":"NLS9781469646688","price":0.0,"currency_code":"GBP","in_stock":true},{"title":"US \/ NEW \/ INGRAM","offer_id":52749805781265,"sku":"NIN9781469646688","price":0.0,"currency_code":"GBP","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0784\/4072\/6801\/files\/1469646684.jpg?v=1753005310"},{"product_id":"abusive-policies-book-mical-raz-9781469661209","title":"Abusive Policies","description":"In the early 1970s, a new wave of public service announcements urged parents to ?help end an American tradition? of child abuse. The message, relayed repeatedly over television and radio, urged abusive parents to seek help. Support groups for parents, including Parents Anonymous, proliferated across the country to deal with the seemingly burgeoning crisis. At the same time, an ever-increasing number of abused children were reported to child welfare agencies, due in part to an expansion of mandatory reporting laws and the creation of reporting hotlines across the nation. Here, Mical Raz examines this history of child abuse policy and charts how it changed since the late 1960s, specifically taking into account the frequency with which agencies removed African American children from their homes and placed them in foster care. Highlighting the rise of Parents Anonymous and connecting their activism to the sexual abuse moral panic that swept the country in the 1980s, Raz argues that these panics and policies?as well as biased viewpoints regarding race, class, and gender?played a powerful role shaping perceptions of child abuse. These perceptions were often directly at odds with the available data and disproportionately targeted poor African American families above others.","brand":"WoB","offers":[{"title":"- \/ - \/ -","offer_id":50630755746065,"sku":"","price":0.0,"currency_code":"GBP","in_stock":true},{"title":"GB \/ NEW \/ GARDNERS","offer_id":50630760005905,"sku":"NGR9781469661209","price":0.0,"currency_code":"GBP","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0784\/4072\/6801\/files\/1469661217_293af266-85ca-430d-b56f-dbc50fe1d481.jpg?v=1763479151"},{"product_id":"sick-and-tired-book-emily-k-abel-9781469661780","title":"Sick and Tired","description":"Medicine finally has discovered fatigue. Recent articles about various diseases conclude that fatigue has been underrecognized, underdiagnosed, and undertreated. Scholars in the social sciences and humanities have also ignored the phenomenon. As a result, we know little about what it means to live with this condition, especially given its diverse symptoms and causes. Emily K. Abel offers the first history of fatigue, one that is scrupulously researched but also informed by her own experiences as a cancer survivor. Abel reveals how the limits of medicine and the American cultural emphasis on productivity intersect to stigmatize those with fatigue. Without an agreed-upon approach to confirm the problem through medical diagnosis, it is difficult to convince others that it is real. When fatigue limits our ability to work, our society sees us as burdens or worse.   With her engaging and informative style, Abel gives us a synthetic history of fatigue and elucidates how it has been ignored or misunderstood, not only by medical professionals but also by American society as a whole.","brand":"WoB","offers":[{"title":"GB \/ NEW \/ GARDNERS","offer_id":50630763282705,"sku":"NGR9781469661780","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"US \/ WELL_READ \/ SBYB","offer_id":51329397850385,"sku":"CIN1469661780A","price":0.0,"currency_code":"GBP","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0784\/4072\/6801\/files\/1469661780.jpg?v=1762595773"},{"product_id":"landscapes-of-care-book-thurka-sangaramoorthy-9781469674179","title":"Landscapes of Care","description":"This insightful work on rural health in the United States examines the ways immigrants, mainly from Latin America and the Caribbean, navigate the health care system in the United States. 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Her extensive ethnographic and policy research shows the personal stories behind health inequity data and helps to give readers a human entry point into the enormous challenges of immigration and rural health.","brand":"WoB","offers":[{"title":"GB \/ NEW \/ GARDNERS","offer_id":50630821904657,"sku":"NGR9781469674179","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"US \/ NEW \/ INGRAM","offer_id":51028562018577,"sku":"NIN9781469674179","price":0.0,"currency_code":"GBP","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0784\/4072\/6801\/files\/1469674173.jpg?v=1752959276"},{"product_id":"in-pursuit-of-health-equity-book-eric-d-carter-9781469674452","title":"In Pursuit of Health Equity","description":"Throughout Latin America, social medicine has been widely recognized for its critical perspectives on mainstream understandings of health and for its progressive policy achievements. Nevertheless, it has been an elusive subject: hard to define, with puzzling historical discontinuities and misconceptions about its origins. Drawing on a vast archive and with an ambitious narrative scope that transcends national borders, Eric D. Carter offers the first comprehensive intellectual and political history of the social medicine movement in Latin America, from the early twentieth century to the present day.  While maintaining a consistent focus on health equity, social medicine has evolved with changing conditions in the region. Carter shows how it shaped early Latin American welfare states, declined with the dominance of midcentury technocratic health planning, resurged in the 1970s in solidarity against authoritarian regimes, and later resisted neoliberal reforms of the health sector. He centers socialist and anarchist doctors, political exiles, intellectuals, populist leaders, and rebellious technocrats from Argentina, Chile, Brazil, and other countries who responded to and shaped a dynamic political environment around health equity. The lessons from this history will inform new thinking about how to achieve health equity in the twenty-first century.","brand":"WoB","offers":[{"title":"GB \/ NEW \/ GARDNERS","offer_id":50630830063889,"sku":"NGR9781469674452","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"US \/ NEW \/ INGRAM","offer_id":51028406305041,"sku":"NIN9781469674452","price":0.0,"currency_code":"GBP","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0784\/4072\/6801\/files\/1469674459.jpg?v=1763479255"},{"product_id":"in-pursuit-of-health-equity-book-eric-d-carter-9781469674445","title":"In Pursuit of Health Equity","description":"Throughout Latin America, social medicine has been widely recognized for its critical perspectives on mainstream understandings of health and for its progressive policy achievements. Nevertheless, it has been an elusive subject: hard to define, with puzzling historical discontinuities and misconceptions about its origins. 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He argues that racist health disparities emerged as a key component of the city's slave-based economy and  quickly became institutionalized with the end of Reconstruction and the rise of Jim Crow. McQueeney also shows that, despite legislation and court victories in the civil rights era, a segregated health care system still exists today.  In addition to charting this history of neglect, McQueeney also suggests pathways to fix the deeply entrenched inequities, taking inspiration from the \"long civil rights\" framework and reconstructing the fight for improved health and access to care that started long before the boycotts, sit-ins, and marches of the 1950s and 1960s. In telling the history of how New Orleans has treated its Black citizens in its hospitals, McQueeney uncovers the broader story of how urban centers across the country have ignored Black Americans and their health needs for the entire history of the nation.","brand":"WoB","offers":[{"title":"GB \/ NEW \/ GARDNERS","offer_id":50630835896593,"sku":"NGR9781469673929","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"US \/ NEW \/ INGRAM","offer_id":51028180140305,"sku":"NIN9781469673929","price":0.0,"currency_code":"GBP","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0784\/4072\/6801\/files\/1469673916.jpg?v=1752986971"},{"product_id":"city-without-care-book-kevin-mcqueeney-9781469673912","title":"A City Without Care","description":"New Orleans is a city that is rich in culture, music, and history. It has also long been a site of some of the most intense racially based medical inequities in the United States. 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In telling the history of how New Orleans has treated its Black citizens in its hospitals, McQueeney uncovers the broader story of how urban centers across the country have ignored Black Americans and their health needs for the entire history of the nation.","brand":"WoB","offers":[{"title":"- \/ - \/ -","offer_id":50630838190353,"sku":"","price":0.0,"currency_code":"GBP","in_stock":true},{"title":"GB \/ NEW \/ GARDNERS","offer_id":50630842253585,"sku":"NGR9781469673912","price":0.0,"currency_code":"GBP","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0784\/4072\/6801\/files\/1469673916_cf408be7-4486-4a15-ac14-01fb51814589.jpg?v=1750956030"},{"product_id":"dying-in-the-city-of-the-blues-book-keith-wailoo-9780807825846","title":"Dying in the City of the Blues","description":"Understanding the connections between culture, race, politics, and disease 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, where one of the nation's first sickle cell clinics was founded in the 1950s, 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.","brand":"WoB","offers":[{"title":"US \/ GOOD \/ SBYB","offer_id":50660680597777,"sku":"CIN0807825840G","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"US \/ WELL_READ \/ SBYB","offer_id":51073190265105,"sku":"CIN0807825840A","price":0.0,"currency_code":"GBP","in_stock":false},{"title":"US \/ VERY_GOOD \/ SBYB","offer_id":51717665456401,"sku":"CIN0807825840VG","price":0.0,"currency_code":"GBP","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0784\/4072\/6801\/files\/0807825840.jpg?v=1764162435"},{"product_id":"prozac-as-a-way-of-life-book-tod-chambers-9780807855515","title":"Prozac As a Way of Life","description":"Prozac and its chemical cousins, Paxil, Celexa, and Zoloft, are some of the most profitable and most widely used drugs in America. Their use in the treatment of a multitude of disorders - from generalized anxiety disorder and premenstrual syndrome to eating disorders and sexual compulsions - has provoked a whirlwind of public debate. Talk shows ask, Why is Prozac so popular? What, exactly, do these drugs treat? But sustained critical discussion among bioethicists and medical humanists has been surprisingly absent. The eleven essays in Prozac as a Way of Life provide the groundwork for a much-needed philosophical discussion of the ethical and cultural dimensions of the popularity of SSRI antidepressants. Focusing on the increasing use of medication as a means of self-enhancement, contributors from the fields of psychiatry, psychology, bioethics, and the medical humanities address issues of identity enhancement, the elasticity of psychiatric diagnosis, and the aggressive marketing campaigns of pharmaceutical companies. They do not question the fact that these antidepressants can, in some cases, provide great benefit to alleviate real suffering. 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