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Criticism of conventional medicine is often regarded as a product of the 1960s. Before then, "scientific medicine" enjoyed uncontestable cultural prestige, with kindly but strict doctors wielding unquestioned authority over grateful patients while "quacks" flogged dubious remedies to the poor and credulous - or so go popular perceptions and - for the most part - received scholarly wisdom. But the very nature of cancer - mysterious, capricious, and deadly - challenged medical authority in the past as much as it does today, and in Negotiating Disease Barbara Clow lays to rest old assumptions about the monopoly of health care by doctors in the first half of the twentieth century. Her detailed analysis of popular beliefs and behaviours reveals the compelling logic of personal decisions about health and healing. Experience and expectation, not fear and ignorance, shaped the health care choices of both cancer sufferers and the "healthy" public. A close examination of three unconventional practitioners in Ontario demonstrates the importance and vitality of alternative medicine. By presenting treatment options that were congenial and plausible to cancer sufferers, these healers contested the authority of conventional medicine. An investigation of government cancer care policy, particularly the activities of Ontario's Commission for the Investigation of Cancer Remedies, exposes the difficulties of defining legitimate health care and the limits of state support for the medical profession. This is, ultimately, a book about who held power in medical encounters in the past. With masterful assurance and a highly readable style, Clow portrays the disputes between sufferers and healers, practitioners and politicians, and legislators and laity that coloured perceptions of medical authority and constrained the power of the profession.
Emerging Illnesses and Society by Randall M. Packard Pdf
"Presenting a theoretical model of the social process of "emerging" illness, the volume's introductory chapter identifies critical factors that shape different trajectories toward the construction of public health priorities. Through case studies of individual diseases and analyses of public awareness campaigns and institutional responses, later chapters provide important insights into the reasons why some illnesses receive more attention and funding than others."--Jacket.
Her detailed analysis of popular beliefs and behaviours reveals the compelling logic of personal decisions about health and healing. Experience and expectation, not fear and ignorance, shaped the health care choices of both cancer sufferers and the "healthy" public. A close examination of three unconventional practitioners in Ontario demonstrates the importance and vitality of alternative medicine. By presenting treatment options that were congenial and plausible to cancer sufferers, these healers contested the authority of conventional medicine. An investigation of government cancer care policy, particularly the activities of Ontario's Commission for the Investigation of Cancer Remedies, exposes the difficulties of defining legitimate health care and the limits of state support for the medical profession. This is, ultimately, a book about who held power in medical encounters in the past. With masterful assurance and a highly readable style, Clow portrays the disputes between sufferers and healers, practitioners and politicians, and legislators and laity that coloured perceptions of medical authority and constrained the power of the profession.
Contributing a unique perspective to health reform, Negotiating Health Care presents the findings of a large qualitative investigation of the experiences of the chronically ill within today′s health care system. The author develops the argument that chronic illness and acute illness are social experiences of a vastly different order that lead to different health care consequences, especially in a health system geared to the "miracle cure." From interviews with chronically ill patients, Thorne discusses the onset of their diseases, handling acute episodes, and their attempts to normalize life. The author also examines the interpersonal experience with health care providers exploring the issues of trust, confidence, and compliance. The institutional experience can, and often does, pose daunting problems for the chronically ill because of organizational and sociocultural issues, health care politics and ideology, and the individual patient′s response to the system. In her concluding chapter, Thorne proposes future directions for health care organization, biomedical technology, and social policy. Students and professionals in the fields of nursing, allied health/medical sciences, and human services will find Negotiating Health Care a valuable resource. "This book is highly recommended for all health care professionals and anyone involved in legislation regarding chronic health care on a national basis. The book also could be very useful for lay people who are chronically ill and for their caregivers and families." --Rehabilitation Nursing "Finally, a window is opened to the experience of chronic illness as it exists within the North American health care system. Just in time. Every health care provider and reformer who looks inside will be changed by the reflections of themselves they see. This book is a courageous voice for both the bolder, more conclusive clinical research and for the chronically ill who may yet show us a better way." --William L. Miller, M.D., The University of Connecticut "Although there are a number of texts available on chronic illness, Dr. Thorne′s approach to the topic is unique in that it provides a graphic illustration of how the beliefs and values guiding the health care system contribute to problems which the chronically ill encounter in obtaining care. By setting the experience of chronic illness in the broader context of the health care system, the [book] provides some clear guidelines for needed changes, something I have not found elsewhere. . . . This is a valuable piece of work . . . which is a valuable contribution to our understanding of chronic illness and which provides a guide both to practice and to health policy revision." --Lee Walker, R.N., Ph.D., The University of Utah "This extraordinary book provides rich description and unique insights into the illness experience. Data obtained from interviews with 91 informants provides remarkable detail, strong linkages to existing theory, and powerful development of the illness trajectory. The book is well documented, methodologically rigorous, and presented in a refreshing style. Dr. Thorne has written a classic! Negotiating Health Care will become the book of the 90s for anyone interested in providing humanistic care." --Jan Morse, R.N., Ph.D., College of Health and Human Development, The Pennsylvania State University "The book provides a view into the major issues adults with chronic illness experience in obtaining health care, a perspective that is rarely available to those of use who use the health care system mainly for acute problems, or indeed, who are the providers. The book is powerful, intense, and often uncomfortable reading; the ′patients′ own words should sensitize all of us who work with the chronically ill. Verbatim accounts of patients′ experiences are woven into a lucid and perceptive view of the structure and organization of Canadian health care, which should be read by health policymakers in all the western industrialized countries." --Juliene G. Lipson, Ph.D., F.A.A.N., University of California, San Francisco "Thorne takes a unique approach in providing a graphic illustration of how the beliefs and values guiding the health care system contribute to the problems the chronically ill encounter in obtaining care. . . . Those concerned with the evolving social and health policy in the United States would be well served in reading Negotiating Health Care." --Academic Library Book Review
Voices of Illness: Negotiating Meaning and Identity by Peter Bray Pdf
This book offers accounts of scholarly interdisciplinary practices and perspectives that examine and discuss the positive potential of attending to the voices and stories of those who live and work with illness in real world settings.
When Carolyn Ellis, a graduate student, and Gene Weinstein, her Professor, fell in love, he was experiencing the first stages of emphysema. As he became increasingly disabled and immobile, these two intensely connected partners fought to maintain their love and to live a meaningful life. They learned to negotiate their daily lives in a way that enabled each of them to feel sufficiently autonomous—him not always like a patient and her not always like a caretaker. Writing as a sociologist, Ellis protrays their life together as a way to understand the complexities of romance, of living with a progressive illness, and, in the final negotiation and reversal of positions, of coping with the loss of a loved one. This rare memoir full of often raw details and emotions becomes an intimate conversation about the intricacies of feeling and relating in a relationship. What Ellis calls experimental ethnography is a finely crafted, forthright, and daring story framed by the author's reflections on writing about and analyzing one's own life. Casting off the safe distance of most social science inquiry, she surrenders the private shroud of a complex relationship to bring sociology closer to literature.
Negotiating the Pandemic by Inayat Ali,Robbie Davis-Floyd Pdf
This book centers on negotiations around cultural, governmental, and individual constructions of COVID-19. It considers how the coronavirus pandemic has been negotiated in different cultures and countries, with the final part of the volume focusing on South Asia and Pakistan in particular. The chapters include auto-ethnographic accounts and ethnographic explorations that reflect upon experiences of living with the pandemic and its implications for all areas of life. The book explicates people’s dealings with COVID-19 at various levels, situates the spread of rumors, conspiracy theories, and new social rituals within micro- and/or macro-contexts, and describes the interplay between the virus and various institutionalized forms of inequalities and structural vulnerabilities. Bringing together a variety of perspectives, the volume relates to the past, describes the Covidian present, and offers futuristic implications. It enlists distinct imaginaries based on current understandings of an extraordinary challenge that holds significant importance for our human future.
Negotiating the French Pox in Early Modern Germany by Claudia Stein Pdf
"Combining medical, religious, economic, municipal and institutional history this book offers a fascinating insight into how early modern society came to terms with disease both in a practical and theoretical sense. This revised English translation of Dr Stein's original German book adds new layers of understanding to a fascinating but complex subject."--BOOK JACKET.
Negotiating Public Health in a Globalized World by David Fairman,Diana Chigas,Elizabeth McClintock,Nick Drager Pdf
Negotiating Public Health in a Globalized World provides health policy-makers with practical information and tools for negotiation, to help them create better international health agreements and programs.
Stephanie L. Kerschbaum,Laura T. Eisenman,James M. Jones
Author : Stephanie L. Kerschbaum,Laura T. Eisenman,James M. Jones Publisher : University of Michigan Press Page : 401 pages File Size : 41,9 Mb Release : 2017-11-15 Category : Education ISBN : 9780472053704
Negotiating Disability by Stephanie L. Kerschbaum,Laura T. Eisenman,James M. Jones Pdf
"Disability is not always central to claims about diversity and inclusion in higher education, but should be. This collection reveals the pervasiveness of disability issues and considerations within many higher education populations and settings, from classrooms to physical environments to policy impacts on students, faculty, administrators, and staff. While disclosing one's disability and identifying shared experiences can engender moments of solidarity, the situation is always complicated by the intersecting factors of race and ethnicity, gender, sexuality, and class. The contributors to Negotiating Disability use disclosure as a statrting point to explore how disability is named, identified, claimed, and negotiated within higher education settings. The essays reflect a broad set of scholarly approaches (e.g., interviews with disabled students and analyses of statistical data) and research interests (e.g., implications for future policy and change, representations of disability in popular culture, literature, and media.)". --Cover.
Negotiating And Navigating Global Health: Case Studies In Global Health Diplomacy by Rosskam Ellen,Kickbusch Ilona Pdf
Diplomacy is undergoing profound changes in the 21st century, and global health is one of the areas where this is most apparent. The negotiation processes that shape and manage the global policy environment for health are increasingly conducted not only between public health experts representing health ministries of nation states but include many other major players at the national level and in the global arena. These include philanthropists and public-private players. As health moves beyond its purely technical realm to become an ever more critical element in foreign policy, security policy, and trade agreements, new skills are needed to negotiate global regimes, international agreements and treaties, and to maintain relations with a wide range of actors.The intent of this book is to provide learning tools for today's broad group of “new health diplomats” in the landscape of this ever-shifting, complex technical and political arena. The case studies are told as the negotiations were experienced by individuals who participated in the various debates, dialogues, negotiations, or by experts who have studied them. This collection fills an important gap in both knowledge and practice providing insight on how negotiations on global health issues have transpired, the successes, challenges, failures, tools and frameworks for negotiation, mechanisms of policy coherence, ways to achieve global health objectives internationally, and how global health diplomacy used as a foreign policy tool can improve relations between nations.
Negotiating the Emotional Challenges of Conducting Deeply Personal Research in Health by Alexandra "Xan" C.H. Nowakowski,J. E. Sumerau Pdf
Public health researchers and clinicians regularly work with people who have suffered physical and mental trauma. Knowing how to conduct a study or treat a patient while navigating deep emotional issues requires special skills and overall awareness of how trauma can impact the process and outcomes of participating in research and/or receiving health care. This book presents a diverse array of case examples from scholars of health-related topics, focusing on biographical narrative as a window into understanding key needs in trauma informed scholarship and medicine. Exploring stories from people of varied backgrounds, experiences, and contexts can help professionals within and beyond the academic research and clinical care spheres create rewarding experiences for patients. Negotiating the Emotional Challenges of Conducting Deeply Personal Research in Health will be of interest to public health practitioners, educators and researchers as well as students.
