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Makes a powerful ethical argument for treating communities as critical moral actors that play key roles in defining and upholding just health policy. Drawing together the key community dimensions of health care, and demonstrating their neglect in most prominent theories of health care justice, Charlene Galarneau postulates the ethical norms of community justice.

The sudden call, the race to the hospital, the high-stakes operation - the drama of transplant surgery is well known. But what happens before and after the surgery? In Transplanting Care, Laura L. Heinemann examines the daily lives of midwestern organ transplant patients and those who care for them, from pretransplant preparations through to the long posttransplant recovery.

Current public health literature suggests that the mentally ill may represent as much as half of the smokers in America. In Smoking Privileges, Laura D. Hirshbein highlights the complex problem of mentally ill smokers, placing it in the context of changes in psychiatry, in the tobacco and pharmaceutical industries, and in the experience of mental illness over the last century.

The 1960s revolutionized American contraceptive practice. Diaphragms, jellies, and condoms with high failure rates gave way to newer choices of the Pill, IUD, and sterilization. This book provides a history of sterilization and what would prove to become, at once, socially divisive and a popular form of birth control.

Chronicles changes in Catholic hospitals during the twentieth century, many of which are emblematic of trends in the US healthcare system. It explores the Church's struggle to safeguard its religious values, examines the power of women, and the gender disparity in these institutions. These critical transformations are situated within the context of changing Church policy during the 1960s.

Traces the growth of depression as an object of medical study and as a consumer commodity. This book addresses gender issues in the construction of depression, explores key questions of how its diagnosis was developed, how it has been used, and how we should question its application in American society.

Fighting around the globe, American soldiers were at high risk for contracting malaria, yet quinine - a natural cure - became harder to acquire. This historical study shows the roots and branches of an enormous drug development project during World War II.

The ability to obtain health care is fundamental to the security, stability, and well-being of poor families. Drawing upon statistical data and interviews with over five hundred families in Oregon, this work assesses the ways in which welfare reform affects the well-being of adults and children who leave the program for work.

In the first decade of the AIDS epidemic, New York City was struck badly. This book presents a social history of New York's AIDS community, and focuses on the ways that these disparate groups formed networks of people and organizations that supported persons with AIDS, reduced transmission, funded research, and gave a face to this epidemic.

Employing historical and contemporary data and case studies, this title examines tonsillectomy, cancer, heart disease, anxiety, and depression, and identify differences between rhetoric and reality and the weaknesses in diagnosis and treatment.

Provides a critical lens through which to view both the contemporary debate about immigration and the US response to the emergent global tuberculosis epidemic. This book shows how the association of the disease with ""tramps"" during the 1880s and 1890s and Dust Bowl refugees during the 1930s provoked exclusionary measures against both groups.

Offers an analysis of public health and family welfare through the lens of the tuberculosis preventorium. This book explains how the child-saving themes embedded in the preventorium movement continue to shape children's health care delivery and family policy in the United States.

Viewing death as a natural event, hospices seek to enable people to live as fully and painlessly as possible. Award-winning medical historian Emily Abel provides insight into several important issues surrounding the growth of hospice care. Using a unique set of records, this book expands our understanding of the history of US hospices.

Examines the working environments of the heartlands of the British and American cotton textile industries from the nineteenth to the late twentieth centuries. Janet Greenlees contends that the air quality within these pioneering workplaces was a key contributor to the health of the wider communities of which they were a part.

Brings together a group of professionals and activists whose lives have been dedicated to health internationalism. By presenting a combination of historical accounts and first-hand reflections, this collection of essays draws attention to the longstanding international activities of the American health left and the lessons they brought home.

At the turn of the twentieth century, Frederick Novy was the leader among a new breed of full-time bacteriologists at American medical schools. Powel H. Kazanjian uses Novy's archived letters, laboratory notebooks, lecture notes, and published works to examine medical research and educational activities during a formative period in modern medical science.

Brings together a group of professionals and activists whose lives have been dedicated to health internationalism. By presenting a combination of historical accounts and first-hand reflections, this collection of essays draws attention to the longstanding international activities of the American health left and the lessons they brought home.

Patients as Policy Actors offers groundbreaking accounts of one of the health field's most important developments of the last fifty years--the rise of more consciously patient-centered care and policymaking. The authors in this volume illustrate, from multiple disciplinary perspectives, the unexpected ways that patients can matter as both agents and objects of health care policy yet nonetheless too often remain silent, silenced, misrepresented, or ignored.

When the new HIPAA privacy rules regarding the release of health information took effect, medical historians suddenly faced a raft of new ethical and legal challenges - even in cases where their subjects had died years, or even a century, earlier. In Privacy and the Past, medical historian Susan C. Lawrence explores the impact of these new privacy rules.

Drawing on oral history interviews, medical journals, newspapers, meeting minutes, and private institutional records, Selling Science sheds light on the ethics of scientific conduct, and on the power of marketing to shape public opinion about medical experimentation.

Shows how various aspects of our understanding and discussion of cancer bears the imprint of its Cold War entanglement.

Neurasthenic Nation investigates how the concept of neurasthenia, the ill effects of modern civilization such as insomnia or impotence, helped doctors and patients, men and women, and advertisers and consumers negotiate changes commonly associated with ï¿¿modernity.ï¿¿ Combining a survey of medical and popular literature on neurasthenia with original research into rare archives of personal letters, patient records, and corporate files, David Schuster charts the emergence of a ï¿¿neurasthenic nationï¿¿â€"a place where people saw their personal health as inextricably tied to the pitfalls and possibilities of a changing world.

Traces how an ever-changing coalition of mental health experts, patients' rights activists, and politicians envisioned the community-based system of psychiatric services. This work shows how policies shifted emphasis from radical reform to incremental change.