Medical

Compassion as Remedy is a quietly revolutionary book about healthcare, ethics, and spiritual practice delivered as a commentary on a 2,500-year-old Tibetan text—the rGyud-bZhi (The Four Tantras), which is the guiding treatise for Traditional Tibetan Medicine. This book, which is a translation of “The Physician Chapter” of rGyud-bZhi, helps readers grasp the essence of healing and teaches healthcare practitioners how to develop limitless compassion, a quality that is essential—as our current healthcare situation makes starkly clear.

Moral development and the practice of compassion should be of great importance to all medical practitioners and “The Physician Chapter” provides detailed instructions, drawn from a millennia-old culture and tradition that is attracting increased attention. Although many books have been written about Ayurveda, Traditional Chinese Medicine, and more, there are very few approachable books regarding the unique features of Tibetan medicine and spiritual and meditation practice.

By integrating healthcare with spiritual practice, Compassion as Remedy provides guidelines for ethics, along with suggestions for developing wisdom and compassion. Throughout the world today, both medical practitioners and their patients are increasingly curious about holistic healing traditions, seeking to find natural, organic, and noninvasive remedies with few side effects. This book shows that compassion itself is a source for the alleviation of suffering.

Dr. Yonten includes examples from his clinical practice, drawn from cross-cultural perspectives and neuroscience, giving readers a rare view of compassion as remedy. In the words of His Holiness the Fourteenth Dalai Lama, one of Dr. Yonten’s teachers, “The ideal physician is one who combines sound medical understanding with compassion and wisdom.”

Firsthand accounts of COVID-19’s devastating effects on working-class communities of color

The first months of the COVID-19 pandemic were filled with talk of heroes, the frontline workers who kept the country functioning. “And when they write those history books, the heroes of the battle will be the hardworking families of New York,” Governor Andrew Cuomo trumpeted on Labor Day 2020. But what if those heroes, those essential workers and their families, wrote the book themselves?

In Until We’re Seen, the heroes write their own stories. Through firsthand accounts by college students at Brooklyn College and California State University Los Angeles, Until We’re Seen chronicles COVID-19’s devastating, disproportionate effects on working-class communities of color, even as the United States has declared the pandemic over and looks away from its impacts.

Very few of these students and their families had the luxury of laboring from home; if they were able to keep their jobs, they took subways and buses, and they worked. They drove delivery trucks, worked in private homes, cooked food in restaurants for people to pick up, worked as EMTs, and did construction. They couldn’t escape to second homes; if anything, more people moved in, as families were forced to consolidate to save money. Together, the accounts in this book show that the COVID-19 pandemic did discriminate, following the race and class fissures endemic to US society. But if these are tales of hardship, they are also love stories—of students’ families, biological and chosen—and of the deep resolve, mundane carework, and herculean efforts such love entails.

Recounting 2020–2022 through the experiences of predominantly young, working-class immigrants and people of color living in the first two major US COVID-19 epicenters, Until We’re Seen spotlights previously untold stories of the pandemic in New York, Los Angeles, and the nation as a whole.

An important analysis of the difference class makes in reproductive health choices

Can you run a marathon, drink coffee, eat fish, or fly on a plane while pregnant? Such questions are just the tip of the iceberg for how most pregnant women’s bodies are managed, surveilled, and scrutinized during pregnancy. The Reproduction of Inequality examines the intense social pressure that expectant and new mothers face when it comes to their health and body-care choices.

Drawing on interviews with dozens of pregnant women and new mothers from poor, middle-class, and mixed-class backgrounds, Katherine Mason paints a vivid picture of the immense weight of expectation that comes with the early stages of motherhood. The women in Mason’s study universally sought to give their children a healthy start in life; however, their chosen approaches varied based on their socio-economic class. Whereas middle-class mothers attempted a complete lifestyle change and absolute devotion to the achievement and maintenance of “the healthy pregnant body,” poorer women made strategic choices about which health goals to prioritize on a limited budget, lacking the economic and cultural capital required to speak and perfectly adhere to the language of “good health.” The unfortunate result is that middle-class mothers are more likely to be seen by others and by themselves as “good” parents, whereas the efforts of working-class mothers are often misread as displaying inadequate concern about their health and that of their child. This in turn contributes to longstanding stereotypes about poor families and communities, and limits their children's chances for upward mobility. The Reproduction of Inequality is a compelling analysis of the impact of class on new mothers’ approaches to health and wellness, and a sobering examination of how inequality shapes mothers’ efforts to maximize their own health and that of their children.

An eye-opening and compelling ethnography about how doctors make decisions

The oath that doctors take to "do no harm" suggests that patient welfare is at the center of what it means to be a successful medical professional. It is also understood, however, that hospitals are not only vessels for medical care—they are businesses, educational institutions, and complex bureaucracies with intricate codes of etiquette that dictate how each staff member should approach situations with patients. In Conflicted Care, Hyeyoung Oh Nelson provides an in-depth look at the decision-making processes of physicians at a large, prestigious academic medical center—that she calls Pacific Medical Center—and finds that more often than not patient wellbeing is only one of several factors governing day-to-day decisions.

The steps physicians take reveal a kind of hidden curriculum of the medical world, one that is guided by status and hierarchy, bureaucracy, norms for consulting with third-parties, regulations for interactions with patients, and medical uncertainty. While at an institutional and individual level patient care continues to be integral to everything the physicians do, they are forced to reconcile that vow with these other, often-conflicting internal logics. Harm, Nelson argues, is thus built into the practice of medicine in the United States. This harm can take the form of unnecessary treatments and consultations or inadequate treatment for pain to motivate specialist intervention that would otherwise be resisted. These and other practices have the overall consequence of significantly driving up inpatient care costs, which then results in patients forgoing needed, ongoing treatment once they receive their medical bills.

Drawing on a deep ethnography of physicians in the Internal Medicine Service unit, Nelson offers a sharp assessment of current policies aimed at alleviating medical costs and explains why they are ineffective. She concludes by offering novel policy and practice recommendations for health care practitioners, policy makers, and healthcare institutions.

Winner, 2025 Thomas & Znaniecki Best Book Award, given by the American Sociological Association International Migration Section

Reveals the presence of an informal system of valuable support and care for marginalized migrants

The United States’ health care system not only consists of a formal safety net, but also an informal and disjointed network of organizations that offer basic care to millions of migrants. This “Third Net” provides free or low-cost health care for the undocumented, low-income, and uninsured migrants who are excluded from the formal system. This groundbreaking study sheds light on the existence of the Third Net and its implications for the overall inequalities in the US health care system.

The Third Net is made up of diverse providers with varying levels of service, organizational culture, and mission. These providers operate in unconventional settings, such as mobile clinics on wheels; pop-up clinics in repurposed spaces; and unlicensed, makeshift clinics run by health activists. Despite their unassuming appearances, these clinics are vital resources for marginalized populations that often go unnoticed by the general public, revealing the shortcomings of our formal health care system.

By examining these alternative health care spaces, the authors expose the inequities entrenched in the broader health care system and urge a reevaluation of it entirely in order to address these injustices.

A bold exposé of how the very foundation of toxicology has been contaminated by sexist and racist ideologies

The first critical understanding of the field of toxicology from a feminist and antiracist perspective, Toxic Sexual Politics asserts that the science of toxicants must be held accountable for the uneven distribution of toxic pollution along racial and sexual lines. Drawing upon in-depth interviews and extensive ethnographic and archival research, including participant observations in toxicology classrooms, conferences, and laboratories, Melina Packer urges environmental health advocates to place toxicant science within its masculinist, militarist, and eugenicist history.

Toxic Sexual Politics shows how the founding fathers of U.S. toxicology were ideologically aligned with the chemical industry, inventing a science that could “make chemicals safe,” as opposed to one that could adequately protect planetary health from toxicants’ hazards. While many toxicologists today are critical of the chemical industry, they continue to rely on the highly limited tools of toxicology as accurate measures of toxicity, as do government regulators, the courts, and environmental advocates.

Unlike most critiques of the chemical industry and narratives of environmental health movements, Toxic Sexual Politics refuses to take the science at face value. By focusing on the sexist, racist, and ableist biases reinforced by toxicology, Packer powerfully argues that this scientific discipline reproduces the very same white supremacist and heterosexist logics that generated environmental injustices in the first place. The field of toxicology can explicitly confront chemical corporate power by building from queer, feminist, anti-ableist, and antiracist movements for environmental and reproductive justice.

Now that the health community is in a state of reflection, how do we put the lessons learned into practice?

As we step back to examine the worldwide response to the COVID-19 pandemic, now is the time to think about how to raise the bar for our response to the next public health emergency. Now is the time to revisit health preparedness strategies and plans. And now is the time to review what the health community did that worked—and how we can do that again.

Learning from COVID-19: GIS for Pandemics tells real-life stories about how spatial thinking became invaluable in both local and full-scale outbreaks during the COVID-19 pandemic.

Needing to answer the question of “where” sat at the forefront of everyone’s mind, and using a geographic information system (GIS) for real-time surveillance transformed possibly overwhelming data into location intelligence that provided agencies and civic leaders with valuable insights. 

Co-edited by Esri chief medical officer Dr. Este Geraghty, this book highlights best practices, key GIS capabilities, and lessons learned during the COVID-19 response that can help communities prepare for the next crisis. GIS has empowered:

• Organizations to use human mobility data to estimate the adherence to social distancing guidelines
• Communities to monitor their health care systems’ capacity through spatially enabled surge tools
• Governments to use location-allocation methods to site new resources (i.e., testing sites and augmented care sites) in ways that account for at-risk and vulnerable populations
• Communities to use maps and spatial analysis to review case trends at local levels to support reopening of economies
• Organizations to think spatially as they consider “back-to-the-workplace” plans that account for physical distancing and employee safety needs

Learning from COVID-19 also includes a “next steps” section that provides ideas, strategies, tools, and actions to help jump-start your own use of GIS, either as a citizen scientist or a health professional. A collection of online resources, including additional stories, videos, new ideas and concepts, and downloadable tools and content, complements this book.

Now is the time to use science and data to make informed decisions for our future, and this book shows us how we can do it.

Explores informal global health action and the importance of intentions of those who volunteer

In the past two decades, medical missions have gained popularity among medical professionals, who view these excursions as important ethical interventions. Indeed, the notion of giving back by volunteering in rural or impoverished communities is celebrated as an ideal act of selflessness, one whose effects are unquestionably beneficial to those being served.

Good Intentions in Global Health is a groundbreaking exploration of the growing realm of informal global health engagement, shedding light on the intricate interplay between intentions, emotions, and ethical considerations. Drawing on fieldwork in Guatemala, Nicole S. Berry investigates those who volunteer for short-term medical missions, revealing how the intent to do good shapes their everyday understandings of their own actions taken in the global health domain.

Berry uncovers how the glorification of medical missions can obscure problems that stem from North American clinicians doctoring in places where they typically do not understand the context. The short-term nature of missions also means that volunteers are not privy to the long-term effects of their actions—the potential harms that may arise from a lack of sustained follow-up care or the utter absence of documentation that they were even there. By relying on gut instincts to reassure themselves that they are doing good, volunteers often bypass a comprehensive assessment of the ethical dimensions underlying their global health work.

Good Intentions in Global Health shows why desires and emotions are increasingly important to contemporary global health. She makes the case that we must pay attention to volunteers’ perceptions of their work, however wrongheaded or naïve, in order to truly influence global health on the ground.

Healthcare providers in the American medical system may find that patients from different cultures bring unfamiliar expectations, anxieties, and needs into the examination room. To provide optimal care for all patients, it is important to see differences from the patient's perspective and to work with patients from a range of demographics. Caring for Patients from Different Cultures has been a vital resource for nurses and physicians for more than twenty years, offering hundreds of case studies that illustrate crosscultural conflicts or misunderstandings as well as examples of culturally competent health care.

Now in its fifth edition, Caring for Patients from Different Cultures covers a wide range of topics, including birth, end of life, communication, traditional medicine, mental health, pain, religion, and multicultural staff challenges. This edition includes more than sixty new cases with an expanded appendix, introduces a new chapter on improving adherence, and updates the concluding chapter with examples of changes various hospitals have made to accommodate cultural differences. Grounded in concepts from the fields of cultural diversity and medical anthropology, Caring for Patients from Different Cultures provides healthcare workers with a frame of reference for understanding cultural differences and sound alternatives for providing the best possible care to multicultural communities.

An inside look at how patients living with terminal illness created one of the country’s first medical marijuana collectives

Marijuana as medicine has been a politically charged topic in this country for more than three decades. Despite overwhelming public support and growing scientific evidence of its therapeutic effects (relief of the nausea caused by chemotherapy for cancer and AIDS, control over seizures or spasticity caused by epilepsy or MS, and relief from chronic and acute pain, to name a few), the drug remains illegal under federal law.

In Dying to Get High, noted sociologist Wendy Chapkis and Richard J. Webb investigate one community of seriously-ill patients fighting the federal government for the right to use physician-recommended marijuana. Based in Santa Cruz, California, the Wo/Men’s Alliance for Medical Marijuana (WAMM) is a unique patient-caregiver cooperative providing marijuana free of charge to mostly terminally ill members. For a brief period in 2004, it even operated the only legal non-governmental medical marijuana garden in the country, protected by the federal courts against the DEA.

Using as their stage this fascinating profile of one remarkable organization, Chapkis and Webb tackle the broader, complex history of medical marijuana in America. Through compelling interviews with patients, public officials, law enforcement officers and physicians, Chapkis and Webb ask what distinguishes a legitimate patient from an illegitimate pothead, good drugs from bad, medicinal effects from just getting high. Dying to Get High combines abstract argument and the messier terrain of how people actually live, suffer and die, and offers a moving account of what is at stake in ongoing debates over the legalization of medical marijuana.

An engaging history of the role that George Washington, Thomas Jefferson, and Benjamin Franklin played in the origins of public health in America

Before the advent of modern antibiotics, one’s life could be abruptly shattered by contagion and death, and debility from infectious diseases and epidemics was commonplace for early Americans, regardless of social status. Concerns over health affected the founding fathers and their families as it did slaves, merchants, immigrants, and everyone else in North America. As both victims of illness and national leaders, the Founders occupied a unique position regarding the development of public health in America. Revolutionary Medicine refocuses the study of the lives of George and Martha Washington, Benjamin Franklin, Thomas Jefferson, John and Abigail Adams, and James and Dolley Madison away from the usual lens of politics to the unique perspective of sickness, health, and medicine in their era. For the founders, republican ideals fostered a reciprocal connection between individual health and the “health” of the nation. Studying the encounters of these American founders with illness and disease, as well as their viewpoints about good health, not only provides us with a richer and more
nuanced insight into their lives, but also opens a window into the practice of medicine in the eighteenth century, which is at once intimate, personal, and first hand. Perhaps most importantly, today’s American public health initiatives have their roots in the work of America’s founders, for they recognized early on that government had compelling reasons to shoulder some new responsibilities with respect to ensuring the health and well-being of its citizenry.

The state of medicine and public healthcare today is still a work in progress, but these founders played a significant role in beginning the conversation that shaped the contours of its development.

Hand in hand with such health crises as HIV/AIDS, breast cancer, and the resurgence of tuberculosis has come an explosion of scientific and medical technologies. As technology documents illness with ever greater precision and clarity, the knowledge and vocabulary of patients is being similarly expanded by activists, consumer advocates, and artists working with new electronic technologies.
Into this breach steps The Visible Woman, collecting professional, academic, and lay viewpoints on gender and the role of visual and textual representation in contemporary health and science. From fetal photography and mammography to mental retardation and chronic fatigue syndrome, The Visible Woman reveals how identities are constructed in medical research and public health initiatives, as well as in popular press accounts of health. New ways of seeing the body, through medical imaging, plastic and sexual surgery, and services for people with disabilities, are all informed, the book argues, by a broader cultural fascination with visuality and media.
Emphasizing the authors' first-hand experiences as medical practitioners, activists, scholars, and patients, The Visible Woman breaks with more established approaches that cast patients as passive objects of medical inquiry, and medical professionals as perpetrators of institutional exploitation in the name of the public good. Asking what it means to be on both ends of the microscope, The Visible Woman highlights the complex perspectives of medical and scientific practitioners who themselves exist both inside and outside their workplaces and professional identities.
The contributors are Michael Bérubé, Lisa Cartwright, Stacie A. Colwell, Richard Cone, Anne Eckman, Valerie Hartouni, Janet Lyon, Emily Martin, Gaye Naismith, Mark Rose, Ella Shohat, Vivian Sobchack, Carol Stabile, Sandy Stone, and Paula A. Treichler.

Do doctors fix patients? Or do they heal them? For all of modern medicine’s many successes, discontent with the quality of patient care has combined with a host of new developments, from aging populations to the resurgence of infectious diseases, which challenge medicine’s overreliance on narrowly mechanistic and technical methods of explanation and intervention, or “fixing’ patients. The need for a better balance, for more humane “healing” rationales and practices that attend to the social and environmental aspects of health and illness and the experiencing person, is more urgent than ever. Yet, in public health and bioethics, the fields best positioned to offer countervailing values and orientations, the dominant approaches largely extend and reinforce the reductionism and individualism of biomedicine.

The collected essays in To Fix or To Heal do more than document the persistence of reductionist approaches and the attendant extension of medicalization to more and more aspects of our lives. The contributors also shed valuable light on why reductionism has persisted and why more holistic models, incorporating social and environmental factors, have gained so little traction. The contributors examine the moral appeal of reductionism, the larger rationalist dream of technological mastery, the growing valuation of health, and the enshrining of individual responsibility as the seemingly non-coercive means of intervention and control. This paradigm-challenging volume advances new lines of criticism of our dominant medical regime, even while proposing ways of bringing medical practice, bioethics, and public health more closely into line with their original goals. Precisely because of the centrality of the biomedical approach to our society, the contributors argue, challenging the reductionist model and its ever-widening effects is perhaps the best way to press for a much-needed renewal of our ethical and political discourse.

What does it mean to oppose AIDS, to be at odds with AIDS? What kind of rupture with history does AIDS represent? How does AIDS and what is said about AIDS relate to gay identity? How does AIDS relate to thinking and acting, particularly deconstructive thinking? The author confronts these questions from a broad philosophical background that ranges from Kant, Nietzsche, Kierkegaard, and Heidegger to contemporary thought concerning gay activism and AIDS research, all brought together in an effort to find a philosophical language capable of doing justice to the singularity of lived experience in the shadow of AIDS.

In examining what AIDS reveals about the conditions of existence, García Düttmann develops the idea of the “dis-unity” or “at-odds-ness” of existence, of the “non-belonging” that characterizes the marginalized, outcast, or abandoned, and exposes human existence itself. He analyzes what AIDS reveals about the character of history through two intertwined issues. First, he examines arguments bearing on the epochal significance of AIDS, the idea that AIDS reveals something uniquely characteristic of our time, hence that the epidemic marks a historical caesura. Second, he develops a theory of historical witnessing suggesting that the phenomena of historical event and bearing witness are not at all separate, but instead are co-originary, inhering in the same complex.

In Discovery and Healing: Reflections on Five Decades of Hematology/Oncology at the Perelman School of Medicine at the University of Pennsylvania, David Vaughn describes the history of the Perelman School of Medicine's Division of Hematology/Oncology. Vaughn knows the subject well: he trained in the Division's Hematology/Oncology fellowship program from 1990 -1993 and has been on the faculty of the Division since 1993.

Since its founding in 1972, the Division of Hematology/Oncology at the Perelman School of Medicine at the University of Pennsylvania has made important contributions to the fields of blood disorders and cancer medicine. Based largely on his personal experience and extensive interviews with former and present faculty, Vaughn describes the evolution of the Division from a small group of research hematologists to a comprehensive program of fundamental and translational researchers and clinical specialists in benign and malignant hematology and solid tumor oncology. He highlights the importance of leadership as he examines the successes of each of the four Division chiefs: Richard "Buz" Cooper, Sanford Shattil, Stephen Emerson, and Lynn Schuchter. He describes the lasting impact that the Division's first oncologist, John Glick, has had on the Division, the Abramson Cancer Center, and the author himself. He emphasizes the important role that philanthropy has played in the Division's achievements. He concludes the account by reflecting on the Division's experience and call to action as it confronted the COVID-19 pandemic.

Both a memoir and a historical account, Vaughn's book demonstrates the good that can be accomplished when an innovative and dedicated medical faculty are committed to discovery and healing.

Written for speech therapists and doctors, this book gives a precise, practical summary of anthroposophical therapeutic speech.

Speech formation, or creative speech, is based on the ancient art of recitation and drama, and was revived and fundamentally redeveloped by Rudolf and Marie Steiner in the early 1920s.

The therapeutic work is based on speech exercises and indications on how to use them, which were given by Rudolf Steiner.

Cartographies of Disease: Maps, Mapping, and Medicine, new expanded edition, is a comprehensive survey of the technology of mapping and its relationship to the battle against disease. This look at medical mapping advances the argument that maps are not merely representations of spatial realities but a way of thinking about relationships between viral and bacterial communities, human hosts, and the environments in which diseases flourish. 

Cartographies of Disease traces the history of medical mapping from its growth in the 19th century during an era of trade and immigration to its renaissance in the 1990s during a new era of globalization. Referencing maps older than John Snow's famous cholera maps of London in the mid-19th century, this survey pulls from the plague maps of the 1600s, while addressing current issues concerning the ability of GIS technology to track diseases worldwide. The original chapters have some minor updating, and two new chapters have been added. Chapter 13 attempts to understand how the hundreds of maps of Ebola revealed not simply disease incidence but the way in which the epidemic itself was perceived. Chapter 14 is about the spatiality of the disease and the means by which different cartographic approaches may affect how infectious outbreaks like ebola can be confronted and contained.

Now, more than ever, professionals can benefit from the power of location data, maps, and analytics in healthcare.  

Health professionals see the importance of the who, what, when, and where of data analytics. The “where” adds a crucial element because good healthcare begins locally and understanding the impacts of place leads to better health. Health professionals recognize the insights gained from visualizing and analyzing location data. Maps, dashboards, apps, and charts can serve as location analytic tools to quantify problems, make predictions, improve operations, assess infrastructure, and make better decisions overall.

GIS Jump Start for Health Professionals is a concise workbook that introduces location analytics available in geographic information systems (GIS) to health professionals, medical students, residents, fellows, nursing students, medical researchers, and others interested in health IT and informatics, health-care administration, and health policy. GIS Jump Start for Health Professionals provides hands-on tutorials that introduce the ArcGIS tools and shows how to use web-based data, storytelling apps, and much more. The book includes concepts and short video lectures to improve learning outcomes. Focused lessons get health professionals up and running quickly and experiencing first hand the value of location data, maps, and analytics.

Written by Kristen S. Kurland, an award-winning professor at Carnegie Mellon University and co-creator of the GIS Tutorial series, this book can be used as a short course or incorporated into another course. It is also valuable to self-learners who want location technology experience. 

In the spring of 1996, when numerous reports of bovine spongioform encephalopathy, popularly known as "mad cow disease," coincided with an outbreak of a similar neuropathological disease in humans, a panic spread across Britain, Europe, and subsequently to the United States. Described as "the biggest crisis the European Union ever had," the mad cow controversy raised important issues about the ways in which risks to the public heath are assessed, disseminated, and controlled. Was the "epidemic" merely a failure of management, the lessons of which could be incorporated into a new strategy for dealing with public anxiety? Was it an isolated case of poor decision-making in a highly volatile economic sector, or was it the kind of nightmare that could face any government responsible for public safety? And what role did the media play in exacerbating an already spiraling crisis?
Divided into four major sections–"Scientific/Historical Perspectives"; "Politics as Health"; "Understanding the Crisis"; and "Lessons and Possibilities" – Mad Cow Crisis assembles the perspectives of a range of experts on this strange and frightening phenomenon, with a view to helping us comprehend how and why such crises occur. Both a careful consideration of how we interpret risk and uncertainty and a step-by-step guide to managing public fear, this important book will interest anyone concerned with public health, communication, science, economics, and medicine.

An extensively researched account of the ups and downs in the history of uppers

Uppers. Crank. Bennies. Dexies. Greenies. Black Beauties. Purple Hearts. Crystal. Ice. And, of course, Speed. Whatever their street names at the moment, amphetamines have been an insistent force in American life since they were marketed as the original antidepressants in the 1930s. On Speed tells the remarkable story of their rise, their fall, and their surprising resurgence. Along the way, it discusses the influence of pharmaceutical marketing on medicine, the evolving scientific understanding of how the human brain works, the role of drugs in maintaining the social order, and the centrality of pills in American life. Above all, however, this is a highly readable biography of a very popular drug. And it is a riveting story.

Incorporating extensive new research, On Speed describes the ups and downs (fittingly, there are mostly ups) in the history of amphetamines, and their remarkable pervasiveness. For example, at the same time that amphetamines were becoming part of the diet of many GIs in World War II, an amphetamine-abusing counterculture began to flourish among civilians. In the 1950s, psychiatrists and family doctors alike prescribed amphetamines for a wide variety of ailments, from mental disorders to obesity to emotional distress. By the late 1960s, speed had become a fixture in everyday life: up to ten percent of Americans were thought to be using amphetamines at least occasionally.

Although their use was regulated in the 1970s, it didn't take long for amphetamines to make a major comeback, with the discovery of Attention Deficit Disorder and the role that one drug in the amphetamine family—Ritalin—could play in treating it. Today’s most popular diet-assistance drugs differ little from the diet pills of years gone by, still speed at their core. And some of our most popular recreational drugs—including the "mellow" drug, Ecstasy—are also amphetamines. Whether we want to admit it or not, writes Rasmussen, we’re still a nation on speed.

Inside today's data-driven personalized medicine, and the time, effort, and information required from patients to make it a reality

Medicine has been personal long before the concept of “personalized medicine” became popular. Health professionals have always taken into consideration the individual characteristics of their patients when diagnosing, and treating them. Patients have cared for themselves and for each other, contributed to medical research, and advocated for new treatments. Given this history, why has the notion of personalized medicine gained so much traction at the beginning of the new millennium?

Personalized Medicine investigates the recent movement for patients’ involvement in how they are treated, diagnosed, and medicated; a movement that accompanies the increasingly popular idea that people should be proactive, well-informed participants in their own healthcare.

While it is often the case that participatory practices in medicine are celebrated as instances of patient empowerment or, alternatively, are dismissed as cases of patient exploitation, Barbara Prainsack challenges these views to illustrate how personalized medicine can give rise to a technology-focused individualism, yet also present new opportunities to strengthen solidarity. Facing the future, this book reveals how medicine informed by digital, quantified, and computable information is already changing the personalization movement, providing a contemporary twist on how medical symptoms or ailments are shared and discussed in society.

Bringing together empirical work and critical scholarship from medicine, public health, data governance, bioethics, and digital sociology, Personalized Medicine analyzes the challenges of personalization driven by patient work and data. This compelling volume proposes an understanding that uses novel technological practices to foreground the needs and interests of patients, instead of being ruled by them.

How the Cuban health care system became the blueprint for accessible medical care around the world

Quiet as it’s kept inside the United States, the Cuban revolution has achieved some phenomenal goals, reclaiming Cuba’s agriculture, advancing its literacy rate to nearly 100 percent – and remaking its medical system. Cuba has transformed its health care to the extent that this “third-world” country has been able to maintain a first-world medical system, whose health indicators surpass those of the United States at a fraction of the cost. Don Fitz combines his deep knowledge of Cuban history with his decades of on-the-ground experience in Cuba to bring us the story of how Cuba’s health care system evolved and how Cuba is tackling the daunting challenges to its revolution in this century.

Fitz weaves together complex themes in Cuban history, moving the reader from one fascinating story to another. He describes how Cuba was able to create a unified system of clinics, and evolved the family doctor-nurse teams that became a model for poor countries throughout the world. How, in the 1980s and ‘90s, Cuba survived the encroachment of AIDS and increasing suffering that came with the collapse of the Soviet Union, and then went on to establish the Latin American School of Medicine, which still brings thousands of international students to the island. Deeply researched, recounted with compassion, Cuban Health Care tells a story you won’t find anywhere else, of how, in terms of caring for everyday people, Cuba’s revolution continues.

Proposes the pragmatic changes we must make to survive COVID and the worst of the new diseases on the horizon

The Trump administration’s neglect and incompetence helped put half-a-million Americans in the ground, dead from COVID-19. Joe Biden was elected president in part on the promise of setting us on a science-driven course correction, but, a little more than a year later, another half-a-million Americans were killed by the virus. What happened? In The Fault in Our SARS, evolutionary epidemiologist Rob Wallace catalogs the Biden administration's failures in controlling the outbreak. He also shows that, beyond matters of specific political persona or party, it was a decades-long structural decline associated with putting profits ahead of people that gutted U.S. public health.

COVID-19 isn’t just an American tragedy. Each in its own way, countries around the world following the "profit-first" model failed their people. Global vaccination campaigns were bottled up by efforts to protect pharmaceutical companies' intellectual property rights. Economies were treated as somehow more real than the people and ecologies upon which they depend. Frustrated populations pushed back against lockdowns, abuses of governmental trust, and, fair or not, the very concept of public health. A social rot meanwhile wended its way into the heart of the sciences that, tasked with controlling disease, serve the systems that helped bring about COVID-19 in the first place.

In The Fault in Our SARS, Wallace and an array of invited contributors aim to strip down the capitalist social psychology that in effect protected the SARS virus. The team proposes instead new approaches in health and ecology that appeal both to humanity's highest ideals and the pragmatic changes we must make to survive COVID and the worst of the new diseases on the horizon.

Businesses that produce bioscience products—gene tests and therapies, pharmaceuticals, vaccines, and medical devices—are regularly confronted with ethical issues concerning these technologies. Conflicts exist between those who support advancements in bioscience and those who fear the consequences of unfettered scientific license. As the debate surrounding bioscience grows, it will be increasingly important for business managers to consider the larger consequences of their work.

This groundbreaking book follows industry research, development, and marketing of medical and bioscience products across a variety of fields, including biotechnology, pharmaceuticals, and bio-agriculture. Compelling and current case studies highlight the ethical decisions business managers frequently face. With the increasing visibility and public expectation placed on businesses in this sector, managers need to understand the ethical and social issues. This book addresses that need and provides a framework for incorporating ethical analysis in business decision making.

Biogenic toxins are fascinating natural products characterized by an enormous diversity of chemical structures and pharmacological activities. They not only pose hazards to humans and animals, but they are important components in the interplay of substances and living beings in nature and, moreover, important sources for new drugs.

Numerous images of plants and chemical structural formulas complete the book, as well as extensive references for further reading.

The multivolume reference is an essential resource for physicians, veterinarians, pharmacists, chemists, biochemists, food chemists and biologists, for students in the relevant fields, and maybe for interested laymen.

All aspects of natural toxins based on the latest scientific knowledge are included:

• All aspects of the toxicology of all living organisms and natural foods, chemistry, action mechanisms, symptoms of intoxications.
• The only book arranged on a strictly scientific base according to the biogenetic origin and chemical structure.

Natural Poisons and Venoms in 5 Volumes:

Volume 1: Plant Toxins: Terpenes and Steroids 2023, ISBN 978-3-11-072472-1

Volume 2: Plant Toxins: Polyketides, Phenylpropanoids and Further Compounds 2024, ISBN 978-3-11-072851-4

Volume 4: Animal Toxins 2023, ISBN 978-3-11-072854-5

Volume 5: Fungal and Microbial Toxins 2025, ISBN 978-3-11-072856-9

Carol Gray combines stick-figures with "conversation symbols" to illustrate what people say and think during conversations. Showing what people are thinking reinforces that others have independent thoughts—a concept that spectrum children don't intuitively understand. Children can also recognize that, although people say one thing, they may think something quite different—another concept foreign to "concrete-thinking" children. Children can draw their own "comic strips" to show what they are thinking and feeling about events or people. Different colors can represent different states of mind. These deceptively simple comic strips can reveal as well as convey quite a lot of substantive information.

The author delves into topics such as:

Feelings and COLOR

Real Answers, Real Strength—Your Guide to Facing Breast Cancer with Clarity and Confidence

A breast cancer diagnosis changes everything. But with the right information—and the right support—you can face it with strength, strategy, and self-compassion.

In Real Talk, Real Hope, breast surgeon Dr. Loren Rourke shares the guidance every patient deserves but rarely receives. Blending medical expertise, empathy, and just enough humor, she delivers essential facts and straight talk to help you move forward with purpose.

You’ll learn what to expect, how to ask the right questions, and why taking care of your whole self is just as critical as treating the disease.

In this empowering guide, you’ll discover:

• What to do in the first days after diagnosis
• The truth about mammograms, risk factors, and screening confusion
• How to build your breast cancer care team
• Why patient education is a key part of healing
• The emotional, physical, and practical realities no one prepares you for

If you or someone you love has been diagnosed with breast cancer, this book offers exactly what the title promises: real talk, and real hope.

In the next decade, six million North American families will be caring for someone with a disability. But other disabled people are not so lucky, left to live in isolation and without support in an era of federal and state cutbacks. This extraordinary book is about the transforming power of family and community on “vulnerable” individuals—the mentally challenged, the mentally ill, the elderly—and how these efforts enrich us as a society. The book tells the stories, interwoven with photographs, of five such people, who are surrounded by social “circles—friends and family whose respect, encouragement, and unconditional love give them a sense of purpose and belonging. Featuring beautiful duotone photographs, the stories told here are profoundly inspiring, giving hope to anyone who, because of age, health, or disability, has been excluded from having a full and meaningful life.

Co-produced with PLAN (Planned Lifetime Advocacy Network).

In recent years, a whole new field of inquiry on the connections between social class and health has arisen from the work of leading social scientists and medical researchers around the world. This pioneering two-volume reader collects for the first time the substance of their main finding: that variations of health within a population are primarily related to sociostructural factors, including income inequality, educational differences, lack of opportunities, and racism.

Featuring sixteen original essays by preeminent researchers in the field, The Society and Population Health Reader: A State and Community Perspective, includes in-depth studies of the links between health and childhood development, race and ethnicity, social status, stress, and other sociocultural factors. It also features a section on the implications of its findings at the state and municipal level, and suggestions for policy changes that would improve health throughout society. Contributors include Michael Marmot, Ichiro Kawachi, Benjamin C. Amick III, J. Fraser Mustard, Richard G. Wilkinson, David R. Williams, Clyde Hertzman, and Stephen B. Fawcett.

Sure to provoke widespread debate and controversy, The Society and Population Health Reader brings to professional, academic, and general readers the most important research findings and dramatic implications for public policy of this fascinating new field.

A companion volume, The Society and Population Health Reader: Income Inequality and Health, edited by Ichiro Kawachi, Bruce P. Kennedy, and Richard G. Wilkinson, is also available from The New Press.

The world of healthcare is constantly evolving, ever increasing in complexity, costs, and stakeholders, and presenting huge challenges to policy making, decision making and system design. In Design for Care, we'll show how service and information designers can work with practice professionals and patients/advocates to make a positive difference in healthcare.

Healthcare Is Changing. Clinicians Must Lead the Way.

Healthcare needs more than innovation—it needs leaders who can connect clinical excellence with operational insight, team culture, and clear vision.

White Coat Leadership helps clinicians step confidently into leadership roles that shape not just teams, but the future of care. Dr. Timothy Liesching introduces a three-dimensional leadership model—palpable, performance, and people leadership—designed to meet today’s most pressing healthcare challenges.

Whether you’re early in your career or already in a leadership seat, this book equips you to lead with clarity, credibility, and compassion.

You’ll learn how to:

• Elevate others while leading without ego
• Balance patient care with strategic decision-making
• Design strong, accountable teams
• Communicate vision that inspires real followership
• Build trust through emotional intelligence and consistency

With practical tools and real-world insights, White Coat Leadership is your prescription for transformative leadership across every level of modern healthcare.

We deserve to be heard, to be genuinely cared for when we go to our medical professionals in pain. It is because of Dr. Seckin and his remarkable team that countless girls and women are now receiving the information and treatment that they need. —Bindi Irwin

Yes, her pain is real. No, she is not crazy. Yes, there is hope.

Although endometriosis is one of the top three causes of female infertility, the average woman with endometriosis is twenty-seven years old before she is accurately diagnosed. The pain is so physically and emotionally insufferable that it can mercilessly affect a woman’s career, social life, relationships, sexual activity, sleep, and diet. It is incurable, but highly treatable. Unfortunately, though, it is rarely treated in a timely manner—if at all—because of misdiagnoses or a lack of education among those in the medical community.

The Doctor Will See You Now is for women determined to let the world know their stories so that every woman with this disease—from the thirteen-year-old girl who is being told that her pain is “part of becoming a woman” to the woman who has been misdiagnosed for decades—knows she is not alone.

The second edition includes five brand new chapters including information on thoracic and sciatic endometriosis, nine new patient stories, updates on fourteen previous patients, a new foreword by Bindi Irwin, new resources, new research, and other updates to make the book more readable and welcoming to readers.

The heroic story of the invention of antidepressants is a key part of the psychopharmaceutical turn. On Trial revolves around one of its pioneers, psychiatrist Roland Kuhn, who practiced in Münsterlingen, a state-run psychiatric hospital in Switzerland. Kuhn became famous for the ‘discovery’ of the first antidepressant, Tofranil, and more recently notorious for his numerous trials on often unsuspecting patients.

Largely based on the extensive and previously inaccessible sources of Kuhn’s private archive, the book delves into the early days of industry-sponsored clinical research in psychiatry. It examines how the clinic, patients, doctors, nursing staff, corporations, and authorities interacted in the trials.

Conducted from the 1940s to 1980s, the Münsterlingen drug trials are historicised and situated in the period’s evolving landscape of experimentation.

This book follows the lives of female Jewish refugees who fled Nazi persecution and became nurses. Nursing was nominally a profession but with its poor pay and harsh discipline, it was unpopular with British women. In the years preceding the Second World War, hospitals in Britain suffered chronic nurse staffing crises. As the country faced inevitable war, the Government and the profession’s elite courted refugees as an antidote to the shortages, but many hospitals refused to employ Continental Jews.
The book explores the changes in the refugees’ status and lives from the war years to the foundation of the National Health Service and to the latter decades of the twentieth century. It places the refugees at the forefront of manoeuvres in nursing practice, education and research at a time of social upheaval and alterations in the position of women.

Becoming a Doctor is the inside story of one person’s transformation from naive student to professorial physician. It will make compelling reading for anyone who, when seeing a doctor, has wondered ‘How did you get to be that way?’

Becoming a Doctor is a personal account of a medical education that began in 1966. It reflects on one person’s experience of being gradually transformed from a nervous student into a professorial physician. The book is not a memoir in the ordinary sense, being less concerned with what the author did than with what education and medical practice did to him.
A doctor’s education may look like a straightforward technical training, but ‘re-membering’ it as a personal experience creates a new and disturbing picture, a blend of joys, absurdities and frustrations. Doctors in the 1960s, as now, were focused on disease and had little to say about suffering, let alone death. They were, and still are, curiously silent about healing, recovery and rehabilitation. From within the hospital, people’s ordinary lives were invisible. Becoming a Doctor shows how difficult it is for a young person to resist the pressures of history and culture.
The author observes his younger self’s efforts to be seen as ‘the right stuff’, which involves suppressing personal feelings, adopting medicine’s rhetoric and mimicking the habits of his teachers, with sometimes disastrous results. Communication, and even empathy, seems like performances in which the doctor’s self need play no part. Later in life, the author becomes more aware of what it is to be present, physically as well as psychologically, to another person.
Becoming a Doctor describes how doctors learn to adopt a compartmentalised concept of human nature that few patients would want. While training as a neurologist, the author is expected to assume that real diseases affect real, physical bodies and that other forms of distress are ‘just psychological’, in other words, unreal. Neurologists appear to be technicians of the brain, psychiatrists of the mind and other doctors of the body.
Each of the book’s chapters focuses on a theme, creating a narrative that is roughly chronological, beginning with the perspectives of a junior medical student and ending with reflections on a doctor’s two major ‘crafts’, diagnosis and treatment. While focused on a particular span of years, the book’s story is in constant conversation with its historical context, a dimension that medical orthodoxy scarcely notices. Reflections are shadowed by theory, but this is not an analytical essay but a piece of provocative and entertaining literature. It is about experiences and dilemmas that matter to everyone.

Die 17. Konferenz über die menschliche Schilddrüse stand ganz im Zeichen der Hypothyreose. Die Schilddrüsenunterfunktion gehört zu den meist verbreiteten Hormonfunktionsstörungen. Besonders betroffen sind ältere Menschen über 60 Jahre. Frauen erkranken deutlich häufiger als Männer. Darüber hinaus weist eins von etwa 3.500 Neugeborenen eine angeborene Hypothyreose auf. Damit ist sie die häufigste Stoffwechselkrankheit bei Neugeborenen. Der Mangel an Schilddrüsenhormonen beeinflusst den ganzen Organismus und hat z.B. Auswirkungen auf Haut und Haar, das Herz-Kreislauf-System und geistige Funktionen. In diesem Buch präsentieren renommierte Wissenschaftler aktuelle und praxisrelevante Ergebnisse zu Ursachen, klinischer Manifestation, Diagnostik und Therapie der Hypothyreose.

A biblical framework for understanding mental illness and helping the mentally ill. Synthesises the relevant biblical material with our scientific understanding of mental illness.

Equips the reader to deal wisely, intelligently and compassionately with issues of mental health in churches and the community. Helps us discern between bad behaviour which is a result of illness and that which results from sin

- How do we deal wisely, intelligently and compassionately with those who suffer from mental illness?

- Can we really make a difference if we aren’t professionals?

- Is it possible to discern between bad behaviour due to illness and that caused by sin

Discover how your church can become a safe, encouraging and healing place.

'The next-best thing to spending a week shadowing Professor Thomas.' Sinclair Ferguson

'Rational, readable and relevant, this book confirms that all involved in pastoral work can help tackle mental illness.' Andrew Fergusson

'The go-to resource for those who want to know more: the wisdom of reliable clinical experience laced with academic rigour and good common sense, all grounded in God’s word. I recommend it highly.' Glynn Harrison

'Empowers us all to play our part.' Debbie Hawker

'An accessible, practical, sensible and biblically grounded resource to help us navigate this challenging terrain.' Sharon James

'Presented in a way that will instil confidence that we can work with mental health professionals.' Nick Pollard

'Alan Thomas has shared his own important insights in what will become a standard book on the subject, accessible and wise.' Geoff Thomas

Authentic Beauty: Defining a New Standard for Care and Results in Plastic Surgery is a groundbreaking book by renowned plastic surgeon Dr. Scott Miller. With over two decades of experience, in Authentic Beauty Dr. Miller shares his philosophy of minimal interventions for maximum results, emphasizing the importance of customized procedures tailored to each patient's unique goals and anatomy.

In his engaging and informative book, Dr. Miller guides readers through the decision-making process, from choosing the right surgeon to understanding the intricacies of facial, breast, and body procedures. He shares patient stories and expert insights, highlighting the transformative power of expertly crafted, naturally beautiful results.

Dr. Miller's passion for performance shines through as he discusses the four pillars of his practice: quality, integrity, safety, and service. He emphasizes the importance of a comprehensive consultation process, where patients' concerns and goals are carefully considered, and personalized treatment plans are developed to achieve optimal outcomes.

Authentic Beauty covers a wide range of topics, including facelifts, breast augmentations, tummy tucks, and minimally invasive procedures such as injectables and laser treatments. Dr. Miller also addresses the unique considerations for male patients seeking cosmetic enhancements.

Throughout the book, Dr. Miller stresses the significance of postoperative care and adherence to recovery guidelines to ensure the best possible results. He provides a wealth of information on maintaining results through proper skincare and a healthy lifestyle.

Whether you're considering a cosmetic procedure or simply curious about the possibilities, Authentic Beauty is an essential resource for anyone seeking to enhance their appearance and embrace life with renewed self-assurance. Discover the power of authentic beauty and learn how to make the best decisions to ensure the best possible result for you.