Exploring the multiple communities of healing among the Tuareg people of Niger, this work examines the beliefs and practices that surround healing and the quest for medicine. In studying ideals of healing that face challenges from wider political and economic forces, the author enables us to understand these culturally and historically constructed processes. This leads us to comprehend how many Tuareg construct and deconstruct local notions of medicine and healers, how patients cope with current problems in health care, and more broadly, how medical knowledge is constructed in anthropology and ethnography.

Rasmussen reveals new perspectives on healing in systems of power and symbolism, bridging interpretive cultural and political economy approaches. This book explores the consequences and implications of the idea that in order to obtain medicine, one must submit to authority, but proceeds beyond merely demonstrating this idea, already largely a truism in anthropology. The Tuareg data show how local residents are not passive victims, but rather active agents in responding to and resisting authority structures of medicine and medical knowledge.

More than sixty years ago, author Dr. Frank G. Moody began treating patients as a second-year medical student at Dartmouth Medical School-Mary Hitchcock Clinic in Hanover, New Hampshire. He was an academic surgeon for the next fifty-five years. In his memoir, Frank Reflections, he offers both a personal and professional overview of his life-his birth in 1928 in New Hampshire; his childhood during the Great Depression; his extensive schooling, both academic and medical; his military service; his experiences serving the sick as a surgical educator; the challenges of his profession; his personal joys of raising three grown children; and his love of skiing and hiking. Recalling a wide range of place, including New York, California Alabama, Utah, and Texas, this memoir communicates Moody's dedication to his craft. Recapping a long and productive, but sometimes winding and turbulent career, Frank Reflections shares insights into Moody's world, in which he tried to enjoy life while helping others get well from their illnesses.

Nathan Smith has struggled with schizophrenia his entire life. Overwhelmed by thoughts of suicide and depression, he disappeared into a haze of alcoholism to deal with the daily challenges of his disease. But instead of alleviating his disease, the alcohol made it ten times worse. Spending most of his time in an alcoholic stupor, he was not in control of his thoughts or actions, thanks to his schizophrenia. Each time he tried to get control of his life, he failed miserably."Mom's Idea" is the heartbreaking story of Smith's struggles to deal with his schizophrenia while ultimately realizing that he also had to find a way to stop drinking. With the encouragement of his mother, he began the long road to sobriety and a more productive life. "Mom's Idea" offers an in-depth account of an average person suffering from schizophrenia; it chronicles the frequently changing ups and downs of dealing with a debilitating disease and the compounding problem of alcoholism.

Today, individuals have greater access to information about their healththaneverbefore(Randeree,2009;Eysenbach,2008).Muchofthis changeisdue, inlargepart, toadvancesinbiotechnologyandtheseque- ing of the human genome (Manolio & Collins, 2009). It is now possible, forexample, forindividualstologontotheInternetand, forafeeofs- eral hundred dollars, order an at-home DNA collection kit and have the resultsofamyriadofgenetictestsdelivereddirectlytotheire-mailinbox (Gurwitz&Bregman-Eschet,2009).Insomecases, thesetestresultsmay indicatepersonalriskforcommonchronicdiseases, suchascertainforms ofcancer, diabetes, cardiovasculardisease, andseveralothers.Companies marketing these test kits often claim that promoting greater access to and awareness of the association between genes and health, and one's genetic susceptibilities to disease, leads to more proactive and insig- fulmethodsofindividualhealthmanagement(Hogarth, Javitt,&Melzer, 2008). Moreover, it is consistent with an emerging trend in medicine - that of consumer-oriented medicine - which places health information toolsdirectlyinthehandsofpatientsunderthepremiseoffosteringbetter patient-providercollaboration(Silvestre, Sue,&Allen,2009). Though the principles behind this direct-to-consumer approach to genetics seem laudable and perhaps even exciting, there is consid- ablecontroversyastowhat, ifany, utilitytheinformationactuallyholds (Geransar&Einsiedel,2008;Wasson, Cook,&Helzlsouer,2006).Unlike geneticteststhatarediagnostic(e.g., chromosomeanalysisforDowns- drome)orhighlypredictive(e.g., BRCA1andBRCA2testingforhereditary breast-ovarian cancer risk), this new wave of presymptomatic predictive genetictestsforcommondiseaseyieldsresultsthataremuchmoreunc- tainbecausethestatisticalmodelsonwhichtheyarepresentlybasedare imperfectandwithlimiteddata(Ng, Murray, Levy,&Venter,2009). Theabovescenarioraisesmanyquestionsfortoday'shealth-carec- sumers. For example, for whom is this information applicable, and for whatpopulationsorsubpopulationsisitnot?Underwhatcircumstances might this information be useful, and when should it be disregarded as irrelevant?Andperhapsmostimportantly, what, ifanything, canbedone inlightofinformationaboutpersonalgeneticrisktoeffectivelylowerthe oddsofbecomingsickandraisetheoddsofstayinghealthy? vii viii PREFACE Becausetheprevalenceofmostdiseasesvariesasafunctionofage, gender, race/ethnicity, and other personal characteristics, answers to these questions are complex and many are just beginning to be und- stood(Khouryetal.,2009).Someexpertshaveconcludedthattheanswers tosuchquestionsremainoutofreachatthepresenttimeandmayc- tinue to be elusive for another 5-10 years (Frazer, Murray, Schork, & Topol,2009).Yet, twenty-?rstcenturyhealth-careconsumers, providers, and policy makers face these choices now about incorporating personal genetic information into health management and often do so without a complete and accurate understanding of the potential impact of their decisionsonmultiplelevels(Carlson,2009).

This volume presents a systematic review of interprofessional education in health and social care. This is accompanied by a wider-ranging critique of interprofessional education, grounded by experience, and informed by sources beyond the evaluations that qualified for inclusion in the review. Synthesising the evidence base for interprofessional education nevertheless remains central, with 353 studies surveyed in the first instance, from which 107 studies form the basis for the final analysis.

The book does much more than amass evidence. It revisits conventional wisdom; setting an agenda to help interested parties perform better by applying lessons learned, remedying weaknesses and renewing efforts to address unanswered questions. The first three chapters set the scene for the systematic review and its findings. The middle section of the book articulates the findings of the review. Finally, the closing chapters consider values and attitudes, theoretical perspectives and offer conclusions.

Identifies optimum conditions for harnessing the benefits of interprofessional education
Offers case studies about interprofessional education worldwide
Provides a glossary to demystify terminology by offering clear definitions

Arguments, assumptions and evidence in this publication are presented to inform policy making, programme planning, teaching and research.

'Successful medical leaders are usually, but not always, experienced and credible clinicians with good people skills, who look beyond the boundaries of their own specialty or institution, who are positive and perseverant and who are prepared to take reasonable risks to achieve their goals. Most importantly they know how to engage their colleagues and effect change. They understand the principles of organisational performance and the balance between professional autonomy and corporate behaviour - ' Sir Bruce Keogh, in the Foreword This book is a comprehensive account of the key aspects of medical leadership. Easy to read and highly accessible, it explores how the medical profession has evolved in tandem with administrative and structural aspects of the NHS: previously reluctant leaders, doctors are increasingly positive about adopting management and organisational responsibility. Assuming leadership roles at all stages of their training and career is a progressively vital component of the definition of a 'good doctor'. Completely up-to-date, this book features exciting and critical developments such as the embedding of the Medical Leadership Competency Framework as a statutory element of the training and development of all doctors, and the establishment of a new Faculty of Medical Leadership and Management. It is highly recommended, inspiring reading for all medical professionals taking on formal leadership roles. Junior doctors, too, will find much of interest.

Through engaging case studies and clear explanations of the underlying science, this book makes the social impacts and ethical consequences of recent advances in biomedicine understandable for general readers. Recent biomedical discoveries promise considerable improvement in the quality of human life, but they also hold the potential to permanently alter society. Are the anticipated benefits worth the price we would have to pay for them? In Where Science and Ethics Meet: Dilemmas at the Frontiers of Medicine and Biology, a biochemist and a biomedical researcher who are highly experienced in explaining ethics for lay audiences present the most innovative advances in biomedicine and enable readers to develop their own opinions about the ethical and social consequences these technologies will bring. Each controversial topic in modern medicine and ethics is introduced through a hypothetical case study that highlights thorny ethical issues before explaining the key aspects of the science and technology involved and addressing the associated ethical considerations in detail. The interdisciplinary treatment of the topics makes the book relevant to students of science, medicine, ethics, law, and sociology as well as health care professionals.

This book sets out to define and consolidate the field of bioinformation studies in its transnational and global dimensions, drawing on debates in science and technology studies, anthropology and sociology. It provides situated analyses of bioinformation journeys across domains and spheres of interpretation. As unprecedented amounts of data relating to biological processes and lives are collected, aggregated, traded and exchanged, infrastructural systems and machine learners produce real consequences as they turn indeterminate data into actionable decisions for states, companies, scientific researchers and consumers. Bioinformation accrues multiple values as it transverses multiple registers and domains, and as it is transformed from bodies to becoming a subject of analysis tied to particular social relations, promises, desires and futures. The volume harnesses the anthropological sensibility for situated, fine-grained, ethnographically grounded analysis to develop an interdisciplinary dialogue on the conceptual, political, social and ethical dimensions posed by bioinformation.

Kidney failure, dialysis, and transplantation are three words that most people hope never to hear in their lifetimes. Mina Gonzales wasn't so lucky. In her memoir, she shares the story of her experiences, a story about choices, destiny, and the ultimate sacrifice that gives life. She knows the pitfalls and setbacks one faces when dealing with the realities of dialysis, organ donation, and kidney transplantation. She recalls those here, along with her journey of personal discovery, family strength, and community involvement. She faced trials and tribulations during dialysis but ultimately emerged victorious, having survived a kidney transplant for more than fifteen years.

Her story could be anyone's story. Along with her experiences, she focuses on facing the truth about life and recognizing the gift that it is. For anyone facing kidney failure, Gonzales provides the information that you need to know. She addresses not only broad questions of life through the lens of her personal experiences, but also specific questions relating to living with kidney failure: What is dialysis? What types are there? How long is a session?

My Choice My Destiny: My Kidney Transplant Journey is intended to be used as a daily spiritual guide to help get through the long hours of dialysis. It is an honest expression of hope that you too will find your donor angel and live a long and healthy life.

Intellectual disability is a generalized disorder appearing before adulthood characterized by significantly impaired cognitive functioning and deficits in two or more adaptive behaviors. With the current limitations in curative treatment for intellectual disabilities, the rehabilitation and management of affected individuals remains a major factor in the management and treatment of symptoms and for the improvement of daily life. Developmental Challenges and Societal Issues for Individuals With Intellectual Disabilities is a comprehensive academic resource that examines treatment and rehabilitation options for those who have intellectual disabilities and examines educational, vocational, and psychosocial needs that can improve quality of life for these individuals. Featuring a range of topics such as comorbidities, epidemiology, and stigma, this book is ideal for psychologists, psychiatrists, pediatricians, psychiatric nurses, clinicians, special ed teachers, social workers, hospital administrators, mental health specialists, managers, academicians, rehabilitation centers, researchers, and students.