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46 books match the query 'Caregiving'

cover of Becoming an Expert Caregiver: How Structural Flaws Shape Autism Carework and Community

Becoming an Expert Caregiver

How Structural Flaws Shape Autism Carework and Community

Cara A. Chiaraluce

Rutgers University Press, 2025

“The hardest thing is dealing with the rest of the world. And we kind of accommodate our lives around that. But the rest of the world doesn’t.” These poignant words were spoken by Charlotte, a mother and primary caregiver of a five-year-old autistic boy, and her words reference the structural arrangements of our world that shape autism carework today. This book features the voices of fifty primary caregivers of autistic and neurodivergent children who illuminate the process through which laywomen become expert caregivers to provide the best care for their children. Expert caregiving captures an intensification of traditional family carework – meeting dependents’ financial, emotional, and physical needs – that transcends the walls of one’s private home and family and challenges the strict boundaries between many worlds: lay and professional, family and work, private and public, medical and social, and individual and society. The process of becoming an expert caregiver spotlights several interesting paradoxes in sociological literature, particularly regarding gender, family, and medicalization, and often forgotten structural flaws in “the rest of the world.”
 
Throughout the chapters in this book, the expert caregiver is one person who faces unbelievably daunting tasks of filling or reforming persistent institutional gaps, primarily in education and health care, and subverting ableist cultural norms. Without institutional support, answers to their questions, or pragmatic avenues to access resources, lay caregivers become the experts. Their trials and tribulations, especially when navigating the boundaries of professional/lay and private/public worlds, illuminate a type of carework that is increasingly relevant to a growing number of young families caring for neurodivergent, disabled, medically fragile, and/or chronically ill children. These stories offer a vivid picture of the often invisible complex challenges and structural forces that drive individuals to become expert caregivers in the first place. 
 
 
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cover of Called to Care?: Health Care, Burnout, and the Search for Meaningful Work

Called to Care?

Health Care, Burnout, and the Search for Meaningful Work

Cindy L. Cain

Rutgers University Press, 2026

Health care workers are burned out. Health care leaders know that workers are burned out but do not yet have the right tools to fix the problem. Called to Care? argues that we can mitigate burnout by examining what is most meaningful about health care work. Using interviews and observation of a wide range of health care workers, Cain shows that workers who care for our most vulnerable adults find their work to be meaningful when they are able to connect to the work and make progress on something that matters. In most cases, these meaningful experiences are also consistent with better care for patients. And yet organizational practices, policy environments, and cultural meanings get in the way of meaningful work, creating burnout. But it doesn’t have to be this way. Called to Care? illustrates that workplaces can and should align meaningful work experiences with quality care for patients.

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cover of Calling Family: Digital Technologies and the Making of Transnational Care Collectives

Calling Family

Digital Technologies and the Making of Transnational Care Collectives

Tanja Ahlin

Rutgers University Press, 2023

How do digital technologies shape both how people care for each other and, through that, who they are? With technological innovation is on the rise and increasing migration introducing vast distances between family members--a situation additionally complicated by the COVID-19 pandemic and the requirements of physical distancing, especially for the most vulnerable – older adults--this is a pertinent question. Through ethnographic fieldwork among families of migrating nurses from Kerala, India, Tanja Ahlin explores how digital technologies shape elder care when adult children and their aging parents live far apart. Coming from a country in which appropriate elder care is closely associated with co-residence, these families tinker with smartphones and social media to establish how care at a distance can and should be done to be considered good. Through the notion of transnational care collectives, Calling Family uncovers the subtle workings of digital technologies on care across countries and continents when being physically together is not feasible. Calling Family provides a better understanding of technological relationality that can only be expected to further intensify in the future.

This book is also freely available online as an open access digital edition. The open access publication was financially supported by the Social Science Research Master and partly also by the Health, Care and the Body Programme Group of the Department of Anthropology, both at the Amsterdam Institute of Social Science Research, University of Amsterdam.
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cover of Cancer and the Politics of Care: Inequalities and Interventions in Global Perspective

Cancer and the Politics of Care

Inequalities and Interventions in Global Perspective

Edited by Linda Rae Bennett, Lenore Manderson, and Belinda Spagnoletti

University College London, 2023

An ethnographic examination of the effects of structural inequalities on cancer treatment around the world.
 
Taking an ethnographic approach, the contributors to this book offer new examinations of cancer and its treatment to show how social, economic, race, gender, and other structural inequalities intersect, compound, and complicate health inequalities. Cancer experiences and impacts are explored across eleven countries: Argentina, Brazil, Denmark, France, Greece, India, Indonesia, Italy, Senegal, the United Kingdom, and the United States. The volume engages with specific cancers from the point of primary prevention to screening, diagnosis, treatment (or its absence), and end-of-life care. Cancer and the Politics of Care traverses new theoretical terrain by explicitly critiquing cancer interventions, their limitations and success, the politics that drive them, and their embeddedness in local cultures and value systems. Its diversity and innovation ensure its wide utility among those working in and studying medical anthropology, social anthropology, and other fields at the intersections of social science, medicine, and health equity.
 
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cover of Care of the Dying Patient

Care of the Dying Patient

Edited by David A. Fleming & John C. Hagan III

University of Missouri Press, 2010

Although the need for improved care for dying patients is widely recognized and frequently discussed, few books address the needs of the physicians, nurses, social workers, therapists, hospice team members, and pastoral counselors involved in care. Care of the Dying Patient contains material not found in other sources, offering advice and solutions to anyone—professional caregiver or family member—confronted with incurable illness and death. Its authors have lectured and published extensively on care of the dying patient and here review a wide range of topics to show that relief of physical suffering is not the only concern in providing care.

This collection encompasses diverse aspects of end-of-life care across multiple disciplines, offering a broad perspective on such central issues as control of pain and other symptoms, spirituality, the needs of caregivers, and special concerns regarding the elderly. In its pages, readers will find out how to:
  • effectively utilize palliative-care services and activate timely referral to hospice,
  • arrange for care that takes into account patients’ cultural beliefs, and
  • respond to spiritual and psychological distress, including the loss of hope that often overshadows physical suffering.
The authors especially emphasize palliative care and hospice, since some physicians fear that such referrals may be viewed by patients and families as abandonment. They also address ethical and legal risks in pain management and warn that fear of overprescribing pain medication may inadvertently lead to ineffective pain relief and even place the treating team at risk of liability for undertreatment of pain.

While physicians have the ability to treat disease, they also help to determine the time and place of death, and they must recognize that end-of-life choices are made more complex than ever before by advances in medicine and at the same time increasingly important. Care of the Dying Patient addresses some of the challenges frequently confronted in terminal care and points the way toward a more compassionate way of death.
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cover of Children as Caregivers: The Global Fight against Tuberculosis and HIV in Zambia

Children as Caregivers

The Global Fight against Tuberculosis and HIV in Zambia

Hunleth, Jean

Rutgers University Press, 2017

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cover of Close to Me, but Far Away: Living with Alzheimer's

Close to Me, but Far Away

Living with Alzheimer's

Burton M. Wheeler

University of Missouri Press, 2001

Each day Burt Wheeler is plagued by the same question. When did it happen? If he could pinpoint the beginning, then he might begin to make peace with himself. He vividly remembers when the doctor diagnosed Kee, his loving wife of over fifty years, with "Alzheimer-type dementia." But, as hard as he tries, it's impossible for him to determine when his wife's dementia started. He remembers her bout with depression, but that, he thinks, was surely due to her breast cancer. There was their dream vacation to Greece when Kee seemed so tired and indifferent. There were the unopened books, when reading had always been such a source of pleasure to her. And, he recalls, the gradual personality changes with friends, and even with family.

Wheeler started writing this book as a form of self-therapy when he found himself thrust into the role of caretaker to his wife--a role for which he felt unprepared. He wrote in memory of the very special woman his wife had been—a wonderful mother, charming and gracious, as well as a deeply respected psychotherapist. She was also his best friend, and he loved her. So, to some degree, this is a love story—a story about two people who have shared life's ups and downs for over fifty years. It's also about commitment.

In Close to Me, but Far Away, Wheeler provides insight into what a caregiver's day is like, as he shares his most intimate thoughts with us. The book provides a window into the author's personal life as he seeks to confront his own ineptitude and the occasional despair he feels as he deals daily with Alzheimer's. He also touches on the question of what keeps him going through times of exhaustion and frustration. Part of his answer lies in holding tenaciously to memories, and part lies in what he believes is a human's extraordinary capacity to continue plodding along simply because he must. Wheeler also believes in rejoicing in the beauty that can be experienced, and he believes in humor, humor achieved only by distancing ourselves from the events that so deeply engage us. And, of course, there is also the indefinable nature of love.

Alzheimer's is a terrifying and horrible disease, as much for loved ones as for the patient. Those who are caregivers or friends of Alzheimer's patients or caregivers will empathize with Burton Wheeler's story. And some might receive comfort from his words or learn from him. Because Alzheimer's is a disease that could affect anyone, Close to Me, but Far Away is a story that should be read by all.

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cover of Decolonial Care: Reimagining Caregiving in the French Caribbean

Decolonial Care

Reimagining Caregiving in the French Caribbean

Jennifer Boum Make

Rutgers University Press, 2025

Decolonial Care examines the relationship between the legacies of colonialism and the dynamics of caregiving that have emerged from the French Caribbean. Through a variety of media, including novels, graphic narratives, and curatorial discourse, this book explores four key contexts at the intersection of care and colonialism: care-focused gender roles, domestic service, nurturing human life and environments, and curation as caring. Decolonial Care argues that to imagine caregiving in the context of the French Caribbean means reckoning with intrinsically uncaring practices inherited from colonial rule that show disregard for human life and environments. Putting in dialogue postcolonial studies and care studies, this book elucidates how caring and uncaring have been historically shaped by colonialism, showing how media and narratives about the French Caribbean document the damaging impact of colonialism but also help develop decolonial approaches to care that sustain human life and livable environments.
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cover of Each Day I Like It Better: Autism, ECT, and the Treatment of Our Most Impaired Children

Each Day I Like It Better

Autism, ECT, and the Treatment of Our Most Impaired Children

Amy S. F. Lutz

Vanderbilt University Press, 2014

In the fall of 2009, Amy Lutz and her husband, Andy, struggled with one of the worst decisions parents could possibly face: whether they could safely keep their autistic ten-year-old son, Jonah, at home any longer. Multiple medication trials, a long procession of behavior modification strategies, and even an almost year-long hospitalization had all failed to control his violent rages. Desperate to stop the attacks that endangered family members, caregivers, and even Jonah himself, Amy and Andy decided to try the controversial procedure of electroconvulsive therapy or ECT. Over the last three years, Jonah has received 136 treatments. His aggression has greatly diminished, and for the first time Jonah, now fourteen, is moving to a less restricted school.


Each Day I Like It Better recounts the journeys of Jonah and seven other children and their families (interviewed by the author) in their quests for appropriate educational placements and therapeutic interventions. The author describes their varied, but mostly successful, experiences with ECT.


A survey of research on pediatric ECT is incorporated into the narrative, and a foreword by child psychiatrist Dirk Dhossche and ECT researcher and practitioner Charles Kellner explains how ECT works, the side effects patients may experience, and its current use in the treatment of autism, catatonia, and violent behavior in children.

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cover of Faith and Mental Health: Religious Resources for Healing

Faith and Mental Health

Religious Resources for Healing

Harold G. Koenig

Templeton Press, 2005

Dr. Harold Koenig opens a window on mental health, providing an unprecedented source of practical information about the relationship between religion and mental health. He examines how Christianity and other world religions deliver mental health services today, and he makes recommendations, based on research, expertise, and experience, for new programs to meet local needs.

Meticulously researched and documented, Faith and Mental Health includes

  • Research on the relationship between religion and positive emotions, psychiatric illnesses, and severe and persistent mental disorders
  • Ways in which religion has influenced mental health historically, and how now and in the future it can be involved with mental health
  • A comprehensive description and categorization of Christian and non-Christian faith-based organizations that provide mental health resources
  • Resources for religious professionals and faith communities on how to design effective programs

Presenting a combination of the history and current research of mental health and religion along with a thorough examination of faith-based organizations operating in the field, this book is a one-of-a-kind resource for the healthcare community; its valuable research and insights will benefit medical and religious professionals, and anyone concerned with the future of mental health care.

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cover of Fighting to Care: Children, Cancer, and Agency in a Pediatric Hospital in Argentina

Fighting to Care

Children, Cancer, and Agency in a Pediatric Hospital in Argentina

Rafael Wainer

Rutgers University Press, 2027

Fighting to Care explores the lived experiences of children with pediatric blood cancer in Argentina, centering the struggles to care from the moment a child is labelled as experiencing "strangeness in the blood.” The book focuses on the notion of "permeable bodies" to understand children’s corporeal and subjective dynamic experience of cancer treatment and interpersonal care. Despite their vulnerability, throughout the course of demanding treatment, children display significant agency, actively navigating their medical journeys through various forms of communication and action. Fighting to Care also highlights the collective forms of care and the personal and interpersonal pain experienced by children, their families, and healthcare professionals in contexts of urgency and against health bureaucracies. In Argentina, caregiving, that is, fighting to care, is deeply intertwined with fighting for health rights within a public healthcare system that, while historically universal and free, is complex and impacted by recurring economic crises and social inequalities.

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cover of Forget Burial: HIV Kinship, Disability, and Queer/Trans Narratives of Care

Forget Burial

HIV Kinship, Disability, and Queer/Trans Narratives of Care

Marty Fink

Rutgers University Press, 2021

Finalist for the LGBTQ Nonfiction Award from Lambda Literary

Queers and trans people in the 1980s and early ‘90s were dying of AIDS and the government failed to care. Lovers, strangers, artists, and community activists came together take care of each other in the face of state violence. In revisiting these histories alongside ongoing queer and trans movements, this book uncovers how early HIV care-giving narratives actually shape how we continue to understand our genders and our disabilities. The queer and trans care-giving kinships that formed in response to HIV continue to inspire how we have sex and build chosen families in the present. In unearthing HIV community newsletters, media, zines, porn, literature, and even vampires, Forget Burial bridges early HIV care-giving activisms with contemporary disability movements. In refusing to bury the legacies of long-term survivors and of those we have lost, this book brings early HIV kinships together with ongoing movements for queer and trans body self-determination.
 
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cover of God's Waiting Room: Racial Reckoning at Life's End

God's Waiting Room

Racial Reckoning at Life's End

Casey Golomski

Rutgers University Press, 2025

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cover of Helping Yourself Help Others: A Book for Caregivers

Helping Yourself Help Others

A Book for Caregivers

Rosalynn Carter

University of Arkansas Press, 2023

“A practical, highly informative, and sympathetic guide.”
—The Washington Post


Most of us will become a caregiver at some point in our lives. And we will assume this role for the most personal reason imaginable: wanting to help someone we love. But we may not know where to start, and we may be afraid of losing ourselves in this daunting task.

Former first lady Rosalynn Carter, a longtime advocate for caregivers and mental health, knows firsthand the challenges of this labor of love. Drawing upon her own experiences and those of hundreds of others whose stories she gathered over many decades, Mrs. Carter offers reassuring, practical advice to any caregiver who has faced stress, anxiety, or loneliness.

Helping Yourself Help Others, reissued here with a new foreword, is as relevant as ever. Long before the COVID-19 pandemic inspired national conversations about the vast undervaluing of unpaid caregiving, the dangers of burnout, and the merits of self-care for relief, Rosalynn Carter was shining a light on these matters and everything else that caregivers confront. Filled with empathy, this encouraging guide will help you meet a difficult challenge head-on and find fulfillment and empowerment in your caregiving role.

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cover of Humanizing Brain Tumors: Strategies for You and Your Physician

Humanizing Brain Tumors

Strategies for You and Your Physician

Edited by Jonathan A. Forbes, Abdelkader Mahammedi, and Soma Sengupta

University of Minnesota Press, 2022

Three practicing doctors present the stories of nine individuals diagnosed with brain tumors.
 
Humanizing Brain Tumors details the lived experiences of patients and their loved ones, from the presentation of symptoms to diagnosis and treatment. These nine test cases and the accompanying compendium offer insight and guidance to anyone living with, caring for, or treating those with brain tumors. Written with a humanistic, yet realistic touch, the authors have created a resource that reminds readers of the important partnership between doctors, patients, and caregivers.
 
This collection delves into our modern understanding of brain tumors, using clinical presentation to illustrate the patient experience and summarize methods of treatment. Imagery, including both MRI scans and medical illustrations, facilitates a vivid description of neuroanatomy. Providing a concise description of modern forms of treatment for patients affected with brain tumors, this book presents a patient-centric perspective.

Humanizing Brain Tumors will appeal to the hundreds of thousands of patients and their loved ones who are affected by brain tumors every year.
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cover of Living in the Land of Limbo: Fiction and Poetry about Family Caregiving

Living in the Land of Limbo

Fiction and Poetry about Family Caregiving

Carol Levine

Vanderbilt University Press, 2014

Living in the Land of Limbo is the first anthology of short stories and poems about family caregivers. These men and women find themselves in "limbo," as they struggle to take care of a family member or friend in the uncertain world of chronic illness. The authors explore caregivers' experiences as they deal with family conflicts, the complexities of the health care system, and the impact of their choices on their lives and the lives of others. The book includes selections devoted to caregivers of aging parents; husbands and wives; ill children; and relatives, lovers, and friends. A final section is devoted to paid caregivers and their clients. Among the conditions that form the background of the selections are dementia, HIV/AIDS, mental illness, multiple sclerosis, and pediatric cancer.

Many of the authors are well-known poets and writers, but others have not been published in mainstream media. They represent a range of cultural backgrounds. Although their works approach caregiving in very different ways, the authors share a commitment to emotional truth, unvarnished by societal ideals of what caregivers should feel and do. These stories and poems paint profoundly moving and revealing portraits of family caregivers.

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cover of Magdalene House: A Place about Mercy

Magdalene House

A Place about Mercy

Sarah VanHooser Suiter

Vanderbilt University Press, 2012

Women come to Magdalene House in Nashville when they are ready to leave the streets. They live togetherunsupervised and free of chargefor two years. During that time, the women are given time, space, and the resources they need to heal from what have often been lifelong experiences with suffering. (Of the twentytwo women now in residence, 80 percent have a diagnosed mental illness other than addiction, 40 percent are receiving treatment for hepatitis C, and onethird are HIV positive.)


However, the story of the Magdalene community is not about these statistics, but about the stories the women tell. They say they thrive in the community because it is a place where they are free to be themselves, safe to give and receive love, and free to speak their trutheven to complain sometimes about how their storytelling is exploited "for the good of the community." A Place about Mercy is a participantobservation account of the history of this remarkable community founded in 1997, its structure, its Thistle Farms beauty products operation, and Reverend Becca Stevens's communal and spiritual vision. The book is finally about what it means to walk the path of healing with a group of unlikely women as guide.


Magdalene House was the subject of a multiplepart documentary on National Public Radio.

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cover of Making Health Care Whole: Integrating Spirituality into Patient Care

Making Health Care Whole

Integrating Spirituality into Patient Care

Christina Puchalski

Templeton Press, 2021

In the last fifteen years, the field of palliative care has experienced a surge in interest in spirituality as an important aspect of caring for seriously ill and dying patients. While spirituality has been generally recognized as an essential dimension of palliative care, uniformity of spiritual care practice has been lacking across health care settings due to factors like varying understandings and definitions of spirituality, lack of resources and practical tools, and limited professional education and training in spiritual care.

In order to address these shortcomings, more than forty spiritual and palliative care experts gathered for a national conference to discuss guidelines for incorporating spirituality into palliative care. Their consensus findings form the basis of Making Health Care Whole. This important new resource provides much-needed definitions and charts a common language for addressing spiritual care across the disciplines of medicine, nursing, social work, chaplaincy, psychology, and other groups. It presents models of spiritual care that are broad and inclusive, and provides tools for screening, assessment, care planning, and interventions. This book also advocates a team approach to spiritual care, and specifies the roles of each professional on the team.
 
Serving as both a scholarly review of the field as well as a practical resource with specific recommendations to improve spiritual care in clinical practice, Making Health Care Whole will benefit hospices and palliative care programs in hospitals, home care services, and long-term care services. It will also be a valuable addition to the curriculum at seminaries, schools of theology, and medical and nursing schools.
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cover of Making Myself at Home in a Nursing Home: Vanderbilt University Press

Making Myself at Home in a Nursing Home

Vanderbilt University Press

Sandra J. Gaffney

Vanderbilt University Press, 2012

Sandra Gaffney entered her first nursing home for long-term care at the unusually young age of fifty. Fourteen years earlier she had been diagnosed with amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease. Over the next sixteen years, Gaffney lived in nursing homes in Florida, Virginia, and Minnesota, as the ways she could be close to family changed.


She describes her situation in these words: "As a nursing home resident, I require total or maximum care. I have limited use of my hands and arms. With special splints, I am able to turn the pages of my books, use the telephone and TV/VCR/FM radio remote control. When my cup is positioned properly, I can drink independently. I am able to walk with a platform walker and the help of two nursing assistants. My walking is not functional; it is only for exercise. After I moved into my third nursing home, I learned to operate a power wheelchair by using an adaptive switch between my knees. ... All other areas of physical care have to be done for me. My speech is impaired. If people listen carefully, they can understand what I am saying. ... I am able to eat regular food and breathe on my own."


Gaffney became an acute observer and strategist about how to live in a nursing home. Her first-person account, dictated to family members and assistants, covers making the decision to enter a nursing home, choosing the right one, and understanding its culture. She talks about how to furnish your room and about all the issues that arise in a resident's typical day. She has much to say about communication with staff and family about "how to help others help me." Gaffney's daughters, Amy and Bridget, and her friend Ellen Potter provide additional perspectives on the caregiving experience.
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cover of Meaning in Suffering: Caring Practices in the Health Professions

Meaning in Suffering

Caring Practices in the Health Professions

Edited by Nancy Johnston and Alwilda Scholler-Jaquish

University of Wisconsin Press, 2007

     Compelling, timely, and essential reading for healthcare providers, Meaning in Suffering addresses the multiplicity of meanings suffering brings to all it touches: patients, families, health workers, and human science professionals. Examining suffering in writing that is both methodologically rigorous and accessible, the contributors preserve first-hand experiences using narrative ethnography, existential hermeneutics, hermeneutic phenomenology, and traditional ethnography. They offer nuanced insights into suffering as a human condition experienced by persons deserving of dignity, empathy, and understanding. Collectively, these essays demonstrate that understanding the suffering of the "other" reveals something vital about the moral courage required to heal—and stay humane—in the face of suffering.
 
 
Winner, Nursing Research Category, American Journal of Nursing
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cover of Migrants Who Care: West Africans Working and Building Lives in U.S. Health Care

Migrants Who Care

West Africans Working and Building Lives in U.S. Health Care

Fumilayo Showers

Rutgers University Press, 2023

As the U.S. population ages and as health care needs become more complex, demand for paid care workers in home and institutional settings has increased. This book draws attention to the reserve of immigrant labor that is called on to meet this need. Migrants Who Care tells the little-known story of a group of English-speaking West African immigrants who have become central to the U.S. health and long-term care systems. With high human capital and middle-class pre-migration backgrounds, these immigrants - hailing from countries as diverse as Cameroon, Sierra Leone, Ghana, Nigeria, and Liberia - encounter blocked opportunities in the U.S. labor market. They then work in the United States, as home health aides, certified nursing assistants, qualified disability support professionals, and licensed practical and registered nurses.

This book reveals the global, political, social, and economic factors that have facilitated the entry of West African women and men into the health care labor force (home and institutional care for older adults and individuals with physical and intellectual disabilities; and skilled nursing). It highlights these immigrants’ role as labor brokers who tap into their local ethnic and immigrant communities to channel co-ethnics to meet this labor demand. It illustrates how West African care workers understand their work across various occupational settings and segments in the health care industry. This book reveals the transformative processes migrants undergo as they become produced, repackaged, and deployed as health care workers after migration.

Ultimately, this book tells the very real and human story of an immigrant group surmounting tremendous obstacles to carve out a labor market niche in health care, providing some of the most essential and intimate aspects of care labor to the most vulnerable members of society.
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cover of Old Age in a New Age: The Promise of Transformative Nursing Homes

Old Age in a New Age

The Promise of Transformative Nursing Homes

Beth Baker

Vanderbilt University Press, 2007

On investigative visits to nursing homes across the nation, Beth Baker has witnessed profound changes. Culture change leaders are tearing up everything—the floor plans, the flow charts, the schedules, the lousy menus, the attitudes, the rules—and starting from scratch. They are creating extraordinary places where people live in dignity and greet the day with contentment, assisted by employees who feel valued and appreciated. Perhaps most surprising, these homes prove that a high quality of life does not have to cost more. Some of the best homes in the nation serve primarily low-income people who are on Medicaid.

In Old Age in a New Age, Baker tell the story of a better way to live in old age. Although each home is different, they share common values: respecting individual choices; empowering staff; fostering a strong community of elders, staff, family members, and volunteers; redesigning buildings from a hospital model to a home (where pets and children are part of everyday life); and honoring people when they die. Her visits to more than two dozen facilities include those associated with the Eden Alternative, Green House, Kendal, and the Pioneer Network. Whether these transformational homes become the norm or the domain of a lucky few is the question that faces the next generation of elders, the baby boomers.
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cover of On the Frontlines of Crisis: Intensive Care and the Challenge of COVID-19

On the Frontlines of Crisis

Intensive Care and the Challenge of COVID-19

Jason Rodriquez

Rutgers University Press, 2025

On the Frontlines of Crisis is a powerful account of the experiences of healthcare workers during the COVID-19 pandemic. As hospitals worldwide became overwhelmed by an influx of critically ill patients, those working in intensive care units (ICUs) were thrust into an unprecedented battle against a deadly virus about which little was understood. Rodriquez takes readers into the heart of two Massachusetts ICUs to learn about the people who put their lives on the line and faced severe challenges as they treated critically ill patients at the peak of the pandemic.
 
A dramatic spike in mental health distress among these healthcare workers was a consequence of the pandemic, but was also a result of the changing dynamics within the healthcare system itself. Here, Rodriquez examines the impact of the development of the contemporary focus on “clinical empathy.” This clinical method, while intended to improve patient care, had profound implications for healthcare workers during the pandemic, often blurring the lines between professional distance and personal involvement, increasing the emotional demands on staff and heightened their vulnerability to anxiety, depression, post-traumatic stress, and burnout. Through the personal stories of those who were in the ICU, On the Frontlines of Crisis offers a sobering reflection on the social and emotional costs of caring for patients.
 
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cover of Parish Nursing - 2011 Edition: Stories of Service and Care

Parish Nursing - 2011 Edition

Stories of Service and Care

Verna Benner Carson

Templeton Press, 2011

The engaging stories in Parish Nursing provide accessible and enjoyable accounts of real parish nurses, both paid and volunteer, who attend to the needs of their congregations in a variety of ways—from home, hospice, and hospital visits to community outreach. This revised edition gathers their stories of hearing and heeding God’s call, of their faith that they are doing the “right thing,” of their joys, sorrows, and challenges, and of their quiet dedication as they offer their time and talents to meet the needs of others.

By offering inspiration and encouragement, along with a healthy dose of updated practical advice, this collection will make parish nursing theory come to life. These stories will honor practicing parish nurses, will guide the way for anyone contemplating parish nursing as a career, and will challenge church members and leaders to examine the role that their congregations play in health ministry—especially in meeting the long-term care needs of an aging population.

 

 

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cover of Parish Nursing: Stories Of Service & Care

Parish Nursing

Stories Of Service & Care

Verna Carson

Templeton Press, 2002

Parish Nursing presents a vision where nurses can serve as the vital link between secular healthcare and sacred faith-based systems. Nurses are able to provide direct ministry to members of the congregation and also can be the communicators, teachers, motivators, and encouragers of others. The parish nurse could be a key person to link the two systems and provide truly wholistic care. Reading the stories of parish nurses gives us hope that this vision might be possible—indeed must be possible—if our aging society is to flourish in the years ahead.
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cover of Playing the Ponies and Other Medical Mysteries Solved

Playing the Ponies and Other Medical Mysteries Solved

Stuart B. Mushlin, MD, FACP

Rutgers University Press, 2017

2017 Choice Outstanding Academic Title

With over forty years of experience as a sought after diagnostician, Dr. Stuart Mushlin has cracked his share of medical mysteries, ones in which there are bigger gambles than playing the ponies at the track. Some of his patients show up with puzzling symptoms, calling for savvy medical detective work. Others seem to present cut-and-dry cases, but they turn out to be suffering from rare or serious conditions.
 
In Playing the Ponies and Other Medical Mysteries Solved, Dr. Mushlin shares some of the most intriguing cases he has encountered, revealing the twists and turns of each patient’s diagnosis and treatment process. Along the way, he imparts the secrets to his success as a medical detective—not specialized high-tech equipment, but time-honored techniques like closely observing, touching, and listening to patients. He also candidly describes cases where he got things wrong, providing readers with honest insights into both the joys and dilemmas of his job.   
 
Dr. Mushlin does not just treat diseases; he treats people. And this is not just a book about the ailments he diagnosed; it is also about the scared, uncertain, ailing individuals he helped in the process. Filled with real-life medical stories you’ll have to read to believe, Playing the Ponies is both a suspenseful page-turner and a heartfelt reflection on a life spent caring for patients. 
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cover of Prayers and Rituals at a Time of Illness and Dying: The Practices of Five World Religions

Prayers and Rituals at a Time of Illness and Dying

The Practices of Five World Religions

Patricia Fosarelli

Templeton Press, 2008

In the course of caring for the ill or dying, health care professionals are sometimes the only ones available to provide spiritual comfort to their patients. In our modern pluralistic society, where patients could come from any number of religious traditions, it can often be difficult to find exactly the right words in these situations.

Prayers and Rituals at a Time of Illness and Dying: The Practices of Five World Religions by experienced physician and theologian Pat Fosarelli offers clear instructions for health care professionals on how to better understand the needs of their Buddhist, Hindu, Muslim, Christian, and Jewish patients during these difficult times. Devoting separate chapters to each tradition, Fosarelli briefly outlines the basic beliefs and then looks at the main tenets of each religion, exploring the varied approaches that they take to illness and end-of-life issues. For each tradition, she also describes practices and offers suitable prayers. Each chapter suggests modifications that may be necessary for Western hospitals, modifications for children, and specific suggestions about what not to do or say in respect to different faith traditions.

This easy-to-use, pocket-sized resource will be referenced again and again by physicians, paramedics, hospital and military chaplains, pastoral counselors, hospice providers, and other medical professionals.

[more]
cover of Restoring the Healer: Spiritual Self-Care for Health Care Professionals

Restoring the Healer

Spiritual Self-Care for Health Care Professionals

William Dorman

Templeton Press, 2015

Burn out. Two words that haunt those in high stress jobs, especially in the medical profession. Long hours and the literal life-and-death nature of the field creates expectations to not only be on call at all hours, but to be at one’s best, even at 3:00 AM after a twenty-hour shift. So much energy is devoted to the care of others that self-care is forgotten.
Yet, more are noticing and research confirms that self-care is needed, not only for personal sanity but also for quality of work. Unwell medical professionals are not the best at treating others. And this self-care includes not just rest, food, and water, but a deeper care, one that tends the spiritual side as well.
To both the spiritually active and the spiritually resistant, hospital chaplain William Dorman offers a guide to understand a more comprehensive, full-bodied self-care. Each chapter begins with case studies, concrete experiences that help unpack abstract concepts which bring much needed peace to stressed individuals. Dorman also structures each chapter to end with prayers and action steps, which offer more concrete ways to care for the self.
From working as a hospital chaplain for over 18 years, and serving as the director of chaplaincy services for the largest integrated health care system in New Mexico, Rev. Dorman recognizes the stresses that come to those who have made it their profession to heal others. Healers need healing too—and this guide is the first step.
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cover of So Far Away: A Daughter's Memoir of Life, Loss, and Love

So Far Away

A Daughter's Memoir of Life, Loss, and Love

Christine W. Hartmann

Vanderbilt University Press, 2011

Christine Hartmann's mother valued control above all else, yet one event appeared beyond her command: the timing of her own death. Not to be denied there either, two decades in advance Irmgard Hartmann chose the date on which to end her life. And her next step was to tell her daughter all about it. For twenty years, Irmgard maintained an unwavering goal, to commit suicide at age seventy. She managed her chronic hypertension, stayed healthy and active, and lived life to the fullest. Meanwhile, Christine fought desperately against the decision. When Irmgard wouldn't listen, the only way to remain part of her life was for Christine to swallow her mother's plans--hook, line, and sinker.

Christine's father, as it turned out, prepared too slowly for old age. Before he had made any decision, fate disabled him through a series of strokes. Confined to a nursing home, severely impaired by dementia and frustrated by his circumstances, his life epitomized the predicament her mother wanted to avoid.

So Far Away gives us an intimate view of a person interacting with and reacting to her parents at the ends of their lives. In a richly detailed, poignant story of family members' separate yet interwoven journeys, it underscores the complexities and opportunities that life presents each one of us.

[more]
cover of Spiritual Caregiving: Healthcare As A Ministry

Spiritual Caregiving

Healthcare As A Ministry

Verna Benner Carson

Templeton Press, 2004

With today's cumbersome insurance procedures, government regulations, endless paperwork, and concerns about malpractice rates, many health care professionals are asking: "Why am I doing this? Am I making a difference to my patients? Is there a better way—and if so, what is it?" In this book, Carson and Koenig examine the state of the health care system with the goal of providing healthcare professionals and caregivers the inspiration and practical tools to reclaim their sense of purpose.

The book begins with an evaluation of the current system from the perspective of the spiritual vision that initially motivated and nourished many caregivers. The authors then pose a vision of a health care system that supports and nurtures the spirituality of patients and their families, of which some elements already exist.

An overview is provided on the preparation necessary for health care professionals to offer spiritual care when there are major implications—for people with chronic illnesses, psychiatric issues, devastating injuries, and those preparing for surgery, facing death, and those living with chronic pain. Also explored are ways that health professionals and caregivers can maintain their own spiritual health even as they work to bring about healing, comfort, and solace to others.

Woven throughout the book are the personal narratives of physicians, nurses, chaplains, health care educators, community resource workers, administrators, therapists, and psychologists—all from a wide range of religious traditions. Their examples inspire and assist professionals in renewing the spiritual focus of health care.

 

[more]
cover of Spiritual Dimensions of Nursing Practice: Revised Edition

Spiritual Dimensions of Nursing Practice

Revised Edition

Verna Benner Carson

Templeton Press, 2008

Ever since the first edition of Verna Benner Carson's Spiritual Dimensions of Nursing Practice went out of print, second-hand copies have been highly sought after by practitioners in the field and nursing school faculty who appreciated the comprehensive scope of the seminal work on spirituality and health. In this highly anticipated revised edition, Carson and her co-editor, Harold G. Koenig, have thoroughly revised and updated this classic in the field.

The revised edition builds on the foundations laid in the first, providing perspectives on new research in the spiritual dimensions of nursing care, applying nursing theory to spiritual care, and addressing the spiritual needs of both nurses and patients. It also examines ethical issues in nursing and the impact of legal decisions on health care issues. Contributors address issues of spiritual development across the entire lifespan—from the spiritual needs and influences of the very young to the elderly, including those facing chronic illnesses or death. The volume takes a similarly broad approach in addressing spiritual issues from a variety of faith backgrounds—including both theistic and pantheistic religious practices, so that nurses can be prepared to meet the needs of patients from various religious traditions.
 
Second to chaplains, nurses are the major providers of spiritual care, and no other book will serve their needs like Spiritual Dimensions of Nursing Practice.
[more]
cover of Spirituality In Patient Care: Why, How, When, and What

Spirituality In Patient Care

Why, How, When, and What

Harold Koenig

Templeton Press, 2002

This book is intended as a guide for practicing physicians, medical students, and residents to help identify and address the spiritual needs of patients. Those who will benefit most will be physicians who wish to know how to integrate spirituality into clinical practice in an effective and sensitive manner. Other professionals, such as nurses and chaplains, may use this book as they interact with doctors, other health professionals, and hospital administrators.

[more]
cover of Spirituality in Patient Care: Why, How, When, and What

Spirituality in Patient Care

Why, How, When, and What

Harold G Koenig

Templeton Press, 2007

 

This landmark handbook for health professionals interested in identifying and addressing the spiritual needs of patients has been significantly revised and expanded. Over the past five years, since the first edition was written, there has been increased research on the relationships among religion, spirituality, and health, and further discussions on the application of these findings to clinical practice. Every section of the book has been rewritten and updated with current research. "I think this version will be my most important contribution to the field of spirituality and health," says Dr. Koenig. "Every bit of what I know about the integration of spirituality into clinical practice, learned over twenty years, is contained in this book."
Koenig addresses the whys, hows, whens, and whats of patient-centered integration of spirituality into patient care, including details on the health-related sacred traditions for each major religious group. He provides health care professionals with the training necessary to screen patients sensitively and competently for spiritual needs, begin to communicate with patients about these issues, and learn when to refer patients to trained spiritual-care professionals who can competently address spiritual needs.
New sections specifically address mental-health professionals, nurses, chaplains and pastoral counselors, social workers, and occupational and physical therapists.
A ten-session model course curriculum on spirituality and health care for medical students and residents is provided, with suggestions on how to adapt it for the training of nurses, social workers, and rehabilitation specialists.

 

[more]
cover of Spirituality in Patient Care: Why, How, When, and What

Spirituality in Patient Care

Why, How, When, and What

Harold G Koenig

Templeton Press, 2013

Praise for the previous edition:
“I highly recommend this book as reading for all physicians and would certainly recommend it for any course on medical ethics and/or required reading for any medical student.”—Journal of the National Medical Association
 
Since the publication of the first edition of Spirituality in Patient Care in 2002, the book has earned a reputation as the authoritative introduction to the subject for health professionals interested in identifying and addressing the spiritual needs of patients. The body of research on religion, spirituality, and health continues to grow at a dramatic rate, creating an urgent need for a new edition of this landmark work. In this, the third edition, Harold G. Koenig, M.D., updates every chapter by incorporating the newest research and introducing sensible ways of translating that research into caring for patients.
 
Like previous editions, this new one addresses the whys, hows, whens, and whats of patient-centered integration of spirituality into patient care so that health professionals, including physicians in primary care and the medical and surgical specialties, can utilize this information in clinical practice. Whole chapters are also included offering profession-specific information for nurses, clergy, mental health professionals, social workers, and occupational and physical therapists. Other chapters address topics like culturally and spiritually sensitive care for each major religious group, potential limitations or barriers to application, and even what may happen when research on spirituality and health is misapplied. Throughout these chapters, readers will find new case histories and clinical examples on how to integrate spirituality into patient care depending on their particular circumstances. A ten-session model course curriculum on spirituality and health care for medical students and residents is also provided, with suggestions on how to adapt it for nursing, social work, physical and occupational therapy, and mental health training programs.
 
For more than ten years Spirituality in Patient Care has offered sound guidance to anyone wishing to do more than simply treat their patients’ physical symptoms. Treating the whole patient often requires becoming something more than just a skilled technician. With this new edition, Dr. Koenig once again shows the way for any health professional seeking to bridge this gap and help patientsregain their lives by finding hope, meaning, and healing.
 
[more]
cover of Testimonios of Care: Feminist Latina/x and Chicana/x Perspectives on Caregiving Praxis

Testimonios of Care

Feminist Latina/x and Chicana/x Perspectives on Caregiving Praxis

Edited by Natalia Deeb-Sossa, Yvette G. Flores, Angie Chabram

University of Arizona Press, 2024

The first English-language collection of Latina/x caregiving testimonios, this volume gives voice to diverse Chicana/x and Latina/x caregiving experiences. Bringing together thirteen first-person accounts, these testimonios speak to the tragic flaws in our health-care system and the woefully undervalued labor of providing care to family and community.

The book opens with an introductory chapter by the three co-editors, and then is divided into three sections exploring the caregiver voice, community caregiving, and reflections that outline a Caregiver Bill of Rights and present a call to action. Throughout, contributors discuss kinship care, including formal and informal adoptions, community care, caregiving in professional health contexts, and the implicit caregiving inherent in teaching BIPOC students, which largely falls upon faculty of color.

Testimonios of Care gives voice to those who often are voiceless in histories of caregiving and is guided by Chicana and Latina feminist principles, which include solidarity between women of color, empathy, willingness to challenge the patriarchal medical health-care systems, questioning traditional gender roles and idealization of familia, and caring for self while caring for loved ones and community.

Contributors
yvonne hurtado allen
Angie Chabram
Natalia Deeb-Sossa
Yvette G. Flores
Inés Hernández-Ávila
ire’ne lara silva
Josie Méndez-Negrete
Maria R. Palacios
Hector Rivera-Lopez
Maria Angelina Soldatenko
Anita Tijerina Revilla
Mónica Torreiro-Casal
Enriqueta Valdez-Curiel
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cover of The Emotional Journey of the Alzheimer's Family

The Emotional Journey of the Alzheimer's Family

Robert B. Santulli and Kesstan Blandin

Dartmouth College Press, 2015

Alzheimer’s disease is a growing public health crisis. According to the Alzheimer’s Association, there are 5.4 million victims of this disease; by 2050, there will be close to 15 million people who suffer from this debilitating disorder of memory, thinking, personality, and functioning. The disease profoundly affects immediate family members, close friends, and neighbors. These people—the Alzheimer’s family—undergo tremendous psychological and emotional change as they witness the cruel and relentless progression of the disease in their loved one. Incorporating over thirty years of experience with Alzheimer’s patients and their families with current medical knowledge, the authors chart the complex emotional journey of the Alzheimer’s family from the onset of the disease through the death of the loved one. They discuss the anger that rises in the face of discordant views of the disease, the defenses that emerge when family members are unwilling to accept a dementia diagnosis, and the common emotions of anxiety, guilt, anger, and shame. They focus especially on grief as the core response to losing a loved one to dementia, and describe the difficult processes of adaptation and acceptance, which lead to personal growth. Final chapters emphasize the importance of establishing a care community and how to understand and cope with personal stress. This volume will be useful to medical professionals and ordinary people close to or caring for a person with dementia.
[more]
cover of The Moon in the Water: Reflections on an Aging Parent

The Moon in the Water

Reflections on an Aging Parent

Kathy J. Phillips

Vanderbilt University Press, 2008

Named a Best Book of 2008 by Library Journal

In a series of moving vignettes, the author begins by describing a particular representation of Water-Moon Kuan Yin, a Buddhist teacher and goddess associated with compassion, who often sits on a precarious overhang or floats on a flimsy petal. Then Kuan Yin steps out of the frame to join the author in the mundane challenges of caring for her father-transferring his health insurance, struggling with a wheelchair van, managing adult diapers, or playing in the fictions of dementia. From perplexed to poignant to funny, the vignettes record the working-class English of a fading but still wise dad, and they find other human versions of Kuan Yin in a doctor who will still make house calls or kind strangers in the street.

The book includes ten illustrations: both classical representations of Kuan Yin and also the author's own drawings, which adapt Kuan Yin in an act of practical spirituality, reading art through life and life through art. Each vignette invites the harried caregiver to take a deep breath and meditate on the trials and joys of caring for an aging parent.

[more]
cover of Transplanting Care: Shifting Commitments in Health and Care in the United States

Transplanting Care

Shifting Commitments in Health and Care in the United States

Heinemann, Laura L.

Rutgers University Press, 2016

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.
 
Heinemann points out that as efforts to control healthcare costs gain urgency—and as new surgical techniques, drug therapies, and home medical equipment advance—most of the transplant process now takes place at home, among kin. Indeed, the transplant system effectively depends on unpaid care labor, typically provided by spouses, parents, siblings, and others. Drawing on scores of interviews with patients, relatives, and healthcare professionals, Heinemann follows a variety of patients and loved ones as they undertake this uncertain and strenuous “transplant journey.” She also shows how these home-based caregiving efforts take place within the larger economic and political context of a paucity of resources for patients and caregivers, who ultimately must surmount numerous obstacles. The author concludes that the many snags encountered by transplant patients and loved ones make a clear case for more comprehensive health and social policy that treats care as a necessarily shared public responsibility.  
 
An illuminating look at the long transplant journey, Transplanting Care also offers broader insight into how we handle infirmity in America—and how we might do a better job of doing so. 
 
[more]
cover of Victories Never Last: Reading and Caregiving in a Time of Plague

Victories Never Last

Reading and Caregiving in a Time of Plague

Robert Zaretsky

University of Chicago Press, 2022

A timely and nuanced book that sets the author’s experience as a nursing home volunteer during the pandemic alongside the wisdom of great thinkers who confronted their own plagues.

In any time of disruption or grief, many of us seek guidance in the work of great writers who endured similar circumstances. During the first year of the COVID-19 pandemic, historian and biographer Robert Zaretsky did the same while also working as a volunteer in a nursing home in south Texas. In Victories Never Last Zaretsky weaves his reflections on the pandemic siege of his nursing home with the testimony of six writers on their own times of plague: Thucydides, Marcus Aurelius, Michel de Montaigne, Daniel Defoe, Mary Shelley, and Albert Camus, whose novel The Plague provides the title of this book.
 
Zaretsky delves into these writers to uncover lessons that can provide deeper insight into our pandemic era. At the same time, he goes beyond the literature to invoke his own experience of the tragedy that enveloped his Texas nursing home, one which first took the form of chronic loneliness and then, inevitably, the deaths of many residents whom we come to know through Zaretsky’s stories. In doing so, Zaretsky shows the power of great literature to connect directly to one’s own life in a different moment and time.
 
For all of us still struggling to comprehend this pandemic and its toll, Zaretsky serves as a thoughtful and down-to-earth guide to the many ways we can come to know and make peace with human suffering.
 
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cover of Welcome to Wherever We Are: A Memoir of Family, Caregiving, and Redemption

Welcome to Wherever We Are

A Memoir of Family, Caregiving, and Redemption

Deborah J. Cohan

Rutgers University Press, 2020

Winner of the 2022 Memoir Prize for Books - Caregiving category​
ESS Public Sociology Award​
Recommended Book in Domestic Violence by DomesticShelters.org

How do you go about caregiving for an ill and elderly parent with a lifelong history of abuse and control, intertwined with expressions of intense love and adoration? How do you reconcile the resulting ambivalence, fear, and anger?
 
Welcome to Wherever We Are is a meditation on what we hold onto, what we let go of, how we remember others and ultimately how we’re remembered. Deborah Cohan shares her story of caring for her father, a man who was simultaneously loud, gentle, loving and cruel and whose brilliant career as an advertising executive included creating slogans like “Hey, how ‘bout a nice Hawaiian punch?” Wrestling with emotional extremes that characterize abusive relationships, Cohan shows how she navigated life with a man who was at once generous and affectionate, creating magical coat pockets filled with chocolate kisses when she was a little girl, yet who was also prone to searing, vicious remarks like “You’d make my life easier if you’d commit suicide.”
 
In this gripping memoir, Cohan tells her unique personal story while also weaving in her expertise as a sociologist and domestic abuse counselor to address broader questions related to marriage, violence, divorce, only children, intimacy and loss. A story most of us can relate to as we reckon with past and future choices against the backdrop of complicated family dynamics, Welcome to Wherever We Are is about how we might come to live our own lives better amidst unpredictable changes through grief and healing.

Questions for Discussion (https://d3tto5i5w9ogdd.cloudfront.net/wp-content/uploads/2020/05/11140346/Cohan_Discussion.docx)
 
[more]
cover of What Do I Say?: Talking with Patients about Spirituality

What Do I Say?

Talking with Patients about Spirituality

Elizabeth Johnston-Taylor

Templeton Press, 2007

Health care professionals, clergy, chaplains, social workers, and others who counsel people in medical crisis often find themselves faced with deeply painful questions: Why is this happening to me? Am I dying? Why should I live? I'm just a burden to others.
Here is a workbook that suggests healing verbal responses to such expressions of spiritual pain. The author, an internationally recognized expert in spiritual caregiving, points out that wanting to help is one motivation for learning these skills, but there are also evidence-based reasons: helping patients express their innermost feelings promotes spiritual healing; spiritual health is related to physical and emotional health; spiritual coping helps patients accept and deal with their illness; and patients tend to want their health care professionals to know about their spirituality.
Lessons, tips, and exercises teach how to listen effectively, with guidelines for detecting and understanding the spiritual needs embedded in patients' conversations. Suggestions are provided for verbal responses to patients who express spiritual distress, including tips for building rapport, using self-disclosure, and praying with patients. A FAQ section deals with frequently asked questions and miscellaneous information, such as:
•What do I do when a patient talks on and on and I have to leave?
•How do I answer a "why" question?
•What do I say to a patient who believes a miracle will happen to cure them?
•What if I'm not religious? How can I talk about it?
By practicing and using these healing techniques, Taylor explains, healthcare professionals will be able to provide patients responses to their questions that allow them to become intellectually, emotionally, and physically aware of their spirituality so they can experience life more fully.
[more]
cover of When Death Is on the Horizon: Temporality, Finitude, and Care Toward Life’s End

When Death Is on the Horizon

Temporality, Finitude, and Care Toward Life’s End

Annemarie Samuels

Rutgers University Press, 2026

The urge to engage with finitude is increasingly central in our present apocalyptic time of political and ecological turmoil. Aging populations and the rapid development of advanced, but expensive, technologies to ever further postpone death pose significant healthcare challenges for societies around the world. In these times, how do people care when the end of life is near? How do they orient toward death? Do they see death as an absolute end, and if not, what sort of horizon does death present? Questioning taken for granted assumptions about end-of-life care, When Death Is on the Horizon analyzes how people approach death in a wide variety of geographical locations and social contexts. Through in-depth ethnographic case studies, it shows how people orient toward, beyond, and away from death, and how they do so within a world marked by historic and ongoing socio-political and structural inequalities.

This book is also freely available online as an open access digital edition.

[more]
cover of Who's Watching?: Daily Practices of Surveillance among Contemporary Families

Who's Watching?

Daily Practices of Surveillance among Contemporary Families

Margaret K. Nelson

Vanderbilt University Press, 2009

Although family members sometime engage in monitoring as an extension of governmental surveillance, they also monitor each other, other families, and their own borders to preserve norms about what a family should be and what family members should do. Whether it is the seemingly benign surveillance of using baby monitors, the more obviously intrusive use of home drug tests on teenagers, or the way people in public feel free to judge and comment on the family composition of others, monitoring goes on all the time -- and even (or maybe especially) when there seems to be no monitoring going on at all.
[more]
cover of With a Little Help from Our Friends: Creating Community as We Grow Older

With a Little Help from Our Friends

Creating Community as We Grow Older

Beth Baker

Vanderbilt University Press, 2014

In this book, an award-winning journalist tells the story of people devising innovative ways to live as they approach retirement, options that ensure they are surrounded by a circle of friends, family, and neighbors. Based on visits and interviews at many communities around the country, Beth Baker weaves a rich tapestry of grassroots alternatives, some of them surprisingly affordable:

• a mobile home cooperative in small-town Oregon
• a senior artists colony in Los Angeles
• neighbors helping neighbors in "Villages" or "naturally occurring retirement communities"
• intentional cohousing communities
• best friends moving in together
• multigenerational families that balance togetherness and privacy
• niche communities including such diverse groups as retired postal workers, gays and lesbians, and Zen Buddhists

Drawing on new research showing the importance of social support to healthy aging and the risks associated with loneliness and isolation, the author encourages the reader to plan for a future with strong connections. Baker explores whether individuals in declining health can really stay rooted in their communities through the end of life and concludes by examining the challenge of expanding the home-care workforce and the potential of new technologies like webcams and assistive robots.

This book is the recipient of the annual Norman L. and Roselea J. Goldberg Prize for the best project in the area of medicine.
[more]
cover of With a Little Help from Our Friends: Creating Community as We Grow Older

With a Little Help from Our Friends

Creating Community as We Grow Older

Beth Baker

Vanderbilt University Press, 2014

In this book, an award-winning journalist tells the story of people devising innovative ways to live as they approach retirement, options that ensure they are surrounded by a circle of friends, family, and neighbors. Based on visits and interviews at many communities around the country, Beth Baker weaves a rich tapestry of grassroots alternatives, some of them surprisingly affordable:

• a mobile home cooperative in small-town Oregon
• a senior artists colony in Los Angeles
• neighbors helping neighbors in "Villages" or "naturally occurring retirement communities"
• intentional cohousing communities
• best friends moving in together
• multigenerational families that balance togetherness and privacy
• niche communities including such diverse groups as retired postal workers, gays and lesbians, and Zen Buddhists

Drawing on new research showing the importance of social support to healthy aging and the risks associated with loneliness and isolation, the author encourages the reader to plan for a future with strong connections. Baker explores whether individuals in declining health can really stay rooted in their communities through the end of life and concludes by examining the challenge of expanding the home-care workforce and the potential of new technologies like webcams and assistive robots.

This book is the recipient of the annual Norman L. and Roselea J. Goldberg Prize for the best project in the area of medicine.
[more]