Kenneth J. Doka – författare

A hands-on guide for patients, families, and caregivers on how tolive an affirming existence while facing the physical and spiritualtraumas of life-threatening illness. Every page of this book reveals the author's keen awareness of thechallenges faced by patients, families, and caregivers dealing withlife threatening illnesses. In page after page readers willdiscover clear, practical, and wise suggestions that are wellgrounded in personal experience. Don't we all know somebody whoneeds this book now?--Robert Kastenbaum, Ph.D., Editor, Omega Journal of Death andDying

Counseling Individuals with Life-Threatening Illness provides a practical guide for counselors who work with clients and families impacted by life-threatening illness. The language and content are appropriate for undergraduate and graduate courses, as well as workshops and trainings for professionals....As the healthcare system continues to evolve, Counseling Individuals with Life-Threatening Illness is a valuable resource for counselors as they find themselves working on interdisciplinary teams with individuals and families impacted by life-threatening illness."--The Professional Counselor JournalWith characteristic clarity, Doka draws on the classic and contemporary literature as well as his own pedagogy and practice in death and dying to offer orienting concepts for the whole spectrum of care people may require when illness intrudes into their lives. For each phase of the illness trajectory...he offers intelligent attention to the problems and prospects people confront, and in countless examples of actual clinical situations he brings to life the concepts that inform compassionate care.From the Foreword by Robert A. Neimeyer, PhDUniversity of MemphisThis book would provide a very good introduction to the psychosocial and spiritual domains for any doctor or nurse coming into palliative care. It provides a lot of information, mixed with some distilled wisdom, as well as a solid grounding about how to relate to these patients and their families in a patient-centered way."--IAHPC Newsletter (International Association for Hospice and Palliative Care)This holistic, family-centered guide to counseling individuals with life-threatening illness considers not only the physical manifestations of the illness, but its psychological, social, economic, and spiritual implications. Revised and updated to reflect the most current research and enhanced theoretical development, this second edition encompasses new therapies that enhance meaning-making at life's end, and offers expanded sections on counseling families during the illness and as they grieve. One of the book's most significant changes involves the adaptation of a model of concurrent care. This model of care has great implications for end-of-life care, bridging the divide between treatment that is primarily palliative and treatment that seeks to cure or extend life. Comprehensive and practical, the book discusses such social and psychological factors as gender, race, ethnicity, social class, education, and intelligence, and how they inform the experience of gravely ill people. The initial crisis of diagnosis is addressed along with unique considerations for those who live with chronic illness, those who are terminally ill, and those who recover. New to This Edition: Generational differences as a source of diversity Expanded sections involving meaning-making strategies (dignity-enhancement therapy, living eulogies, reminiscence therapy, life review, meaning-centered therapy, moral/ethical issues, and heart wills) Discussion of end-of-life phenomena and ways to assist patient and family in interpreting and responding to them Enhanced coverage of caregiver issues Expanded discussion of spirituality Additional behavioral strategies to assist pain management Anticipatory mourning Post-death grief for family members Chronic care and rehabilitation Incorporates Rand Study on Concurrent Care and other new models

Produced as a companion to the Hospice Foundation of America's fifth annual National Bereavement Teleconference, this volume examines how key aspects of identity affect how individuals grieve. Variables explored include culture, spirituality, age and development level, class and gender.

Assesses the needs and lives of the first generation of people with developmental disabilities who have survived into later life. Describes the challenges facing practitioners in gerontology and developmental disabilities to modify programs designed for mid-life adults, and notes that senior services will need to incorporate the needs of the new po

The third edition of Grieving Beyond Gender explores the different ways that individuals grieve, noting that gender is only one factor that affects an individual’s style or pattern of grief.Inherent in the concept of grieving styles is a notion that gender is fluid and that traditional binary views of gender are belied by the concept of grieving styles, and this is highlighted and explored in more depth in the new edition. Doka and Martin present a model firmly grounded in social science theory and research, and place special emphasis on the model’s clinical implications. Clinicians will come away from this book with concrete tools for supporting different types of grievers through individual counseling or group support.

The third edition of Grieving Beyond Gender explores the different ways that individuals grieve, noting that gender is only one factor that affects an individual’s style or pattern of grief.Inherent in the concept of grieving styles is a notion that gender is fluid and that traditional binary views of gender are belied by the concept of grieving styles, and this is highlighted and explored in more depth in the new edition. Doka and Martin present a model firmly grounded in social science theory and research, and place special emphasis on the model’s clinical implications. Clinicians will come away from this book with concrete tools for supporting different types of grievers through individual counseling or group support.

Historically, AIDS is just one of a series of dreaded diseases that have aroused both great fear and irrational actions. The previous diseases, including bubonic plague, syphilis, tuberculosis, leprosy and cancer, have evoked such a sense of dread that rational moves to halt the disease have become compromised.; This text examines the deep sense of fear that AIDS evokes, stigmatizing those who suffer from the disease, as well as their families and caregivers. Until AIDS can be seen for what it actually is - a life-threatening disease - policies providing for humane treatment will not evolve. The book also emphasizes that diseases are more than biological phenomena or individual catastrophes - they are profoundly social events. The ways in which diseases are spread and treated are strongly influenced by larger sociological considerations, and they may have the capacity to change social institutions or society Itself. Rooting Aids In The History Of Diseases, The First Part Of The book reviews the nature, history and responses of earlier dreaded diseases. The next section examines AIDS itself, proposed as the archetypal dreaded disease. Already creating a sense of panic, AIDS is also shown to be a social disease, likely to have significant effects on the social order. Thus, only by containing the epidemic of fear and controlling the resulting irrationality, can the AIDS epidemic be halted.

Historically, AIDS is just one of a series of dreaded diseases that have aroused both great fear and irrational actions. The previous diseases, including bubonic plague, syphilis, tuberculosis, leprosy and cancer, have evoked such a sense of dread that rational moves to halt the disease have become compromised.; This text examines the deep sense of fear that AIDS evokes, stigmatizing those who suffer from the disease, as well as their families and caregivers. Until AIDS can be seen for what it actually is - a life-threatening disease - policies providing for humane treatment will not evolve. The book also emphasizes that diseases are more than biological phenomena or individual catastrophes - they are profoundly social events. The ways in which diseases are spread and treated are strongly influenced by larger sociological considerations, and they may have the capacity to change social institutions or society Itself. Rooting Aids In The History Of Diseases, The First Part Of The book reviews the nature, history and responses of earlier dreaded diseases. The next section examines AIDS itself, proposed as the archetypal dreaded disease. Already creating a sense of panic, AIDS is also shown to be a social disease, likely to have significant effects on the social order. Thus, only by containing the epidemic of fear and controlling the resulting irrationality, can the AIDS epidemic be halted.

Based on the Hospice Foundation of America's second annual teleconference, this book explores three basic themes in children's grief. Firstly, it maintains that children are always developing; therefore their understanding of death and their reactions to illness and loss are also multifaceted and constantly undergoing change. Secondly, children grieve in ways that are both different from and similar to adults. While they may need different therapeutic approaches from their elders, each loss is different and the grief experience will be affected by many of the same factors that affect adults. Thirdly, it holds that they need significant support as they grieve.; Talking to children about loss and and illness is too important to wait until a crisis; rather, it is essential to provide opportunities to discuss loss in times that are not so Emotionally Laden. This Book Aims To Demonstrate That Open Communication between parents and children will lead to skills and understanding that are essential to the child for coping with loss and reaffirming that death is part of the process of living.

First published in 1996. This book was produced as a companion to the Hospice Foundation of America's third annual teleconference. The Foundation, begun in 1982, is a nonprofit organization dedicated to providing leadership in the development of hospice and its philosophy of care for terminally ill people. The Foundation conducts educational programs related to hospice, sponsors research on ethical questions as well as the economics of health care at the end-of-life, and serves as a philanthropic presence within the national hospice community. Close to 90 percent of hospices in the United States reach beyond their own patients and families to become, in a variety of ways, a community resource on grief and bereavement That is part of the hospice mission and an important service which the Hospice Foundation of America encourages and tries to support Our annual teleconference is a major part of our effort and it, like all of our projects, is largely underwritten by contributions from individuals. The Hospice Foundation of America is a member of the Combined Federal Campaign through Health Charities of Americas. The Hospice Foundation of America is a member of the Combined Federal Campaign through Health Charities of America.

Living With Grief: Children, Adolescents, and Loss, (2000) edited by Kenneth J. Doka, features articles by leading educators and clinicians in the field of grief and bereavement. The chapters entitled "Voices" are the writings of children and adolescents. The book includes a comprehensive resource list of national organizations and a useful bibliography of age-appropriate literature for children and adolescents.

While we often discuss how we grieve, rarely do we consider the places where we grieve. Yet whether at work, at school, at worship or at home, grief not only affects our moods and motivation but our ability to function and our relationships as well. This book considers the ways that grief influences us in varied settings, offering humane and practical suggestions to organizations such as workplaces, schools or places of worship as to how they can assist grievers in their midst struggling with illness and loss.  First published in 1999. Routledge is an imprint of Taylor & Francis, an informa company.

While we often discuss how we grieve, rarely do we consider the places where we grieve. Yet whether at work, at school, at worship or at home, grief not only affects our moods and motivation but our ability to function and our relationships as well. This book considers the ways that grief influences us in varied settings, offering humane and practical suggestions to organizations such as workplaces, schools or places of worship as to how they can assist grievers in their midst struggling with illness and loss.  First published in 1999. Routledge is an imprint of Taylor & Francis, an informa company.

This book was produced as a companion to the Hospice Foundation of America''s fourth annual national bereavement teleconference. Hospice Foundation of America is a nonprofit organization dedicated to providing leadership in the development of hospice and its philosophy of care for terminally-ill people. Through education, research, and philanthroptc programs, The Hospice Foundation of America assists those who cope either personally or professionally with terminal illness and the process of death, grief and bereavement. In addition to the annual teleconference, the Foundation publishes Journeys, a monthly newsletter to help in bereavement; produces A Guide to Recalling and Telling Your Life Story, a tool to assist people in writing their autobiographies; and provides a number of free informational brochures on hospices, military service centers, and other organizations. The Foundation is developing an audiotape series entitled Clergy to Clergy to help clergy members learn more about grief and bereavement issues.

This book was produced as a companion to the Hospice Foundation of America''s fourth annual national bereavement teleconference. Hospice Foundation of America is a nonprofit organization dedicated to providing leadership in the development of hospice and its philosophy of care for terminally-ill people. Through education, research, and philanthroptc programs, The Hospice Foundation of America assists those who cope either personally or professionally with terminal illness and the process of death, grief and bereavement. In addition to the annual teleconference, the Foundation publishes Journeys, a monthly newsletter to help in bereavement; produces A Guide to Recalling and Telling Your Life Story, a tool to assist people in writing their autobiographies; and provides a number of free informational brochures on hospices, military service centers, and other organizations. The Foundation is developing an audiotape series entitled Clergy to Clergy to help clergy members learn more about grief and bereavement issues.

First published in 1996. This book was produced as a companion to the Hospice Foundation of America''s third annual teleconference. The Foundation, begun in 1982, is a nonprofit organization dedicated to providing leadership in the development of hospice and its philosophy of care for terminally ill people. The Foundation conducts educational programs related to hospice, sponsors research on ethical questions as well as the economics of health care at the end-of-life, and serves as a philanthropic presence within the national hospice community. Close to 90 percent of hospices in the United States reach beyond their own patients and families to become, in a variety of ways, a community resource on grief and bereavement That is part of the hospice mission and an important service which the Hospice Foundation of America encourages and tries to support Our annual teleconference is a major part of our effort and it, like all of our projects, is largely underwritten by contributions from individuals. The Hospice Foundation of America is a member of the Combined Federal Campaign through Health Charities of Americas. The Hospice Foundation of America is a member of the Combined Federal Campaign through Health Charities of America.

First published in 1996. This book was produced as a companion to the Hospice Foundation of America''s third annual teleconference. The Foundation, begun in 1982, is a nonprofit organization dedicated to providing leadership in the development of hospice and its philosophy of care for terminally ill people. The Foundation conducts educational programs related to hospice, sponsors research on ethical questions as well as the economics of health care at the end-of-life, and serves as a philanthropic presence within the national hospice community. Close to 90 percent of hospices in the United States reach beyond their own patients and families to become, in a variety of ways, a community resource on grief and bereavement That is part of the hospice mission and an important service which the Hospice Foundation of America encourages and tries to support Our annual teleconference is a major part of our effort and it, like all of our projects, is largely underwritten by contributions from individuals. The Hospice Foundation of America is a member of the Combined Federal Campaign through Health Charities of Americas. The Hospice Foundation of America is a member of the Combined Federal Campaign through Health Charities of America.

Based on the Hospice Foundation of America''s second annual teleconference, this book explores three basic themes in children''s grief. Firstly, it maintains that children are always developing; therefore their understanding of death and their reactions to illness and loss are also multifaceted and constantly undergoing change. Secondly, children grieve in ways that are both different from and similar to adults. While they may need different therapeutic approaches from their elders, each loss is different and the grief experience will be affected by many of the same factors that affect adults. Thirdly, it holds that they need significant support as they grieve.; Talking to children about loss and and illness is too important to wait until a crisis; rather, it is essential to provide opportunities to discuss loss in times that are not so Emotionally Laden. This Book Aims To Demonstrate That Open Communication between parents and children will lead to skills and understanding that are essential to the child for coping with loss and reaffirming that death is part of the process of living.

Based on the Hospice Foundation of America''s second annual teleconference, this book explores three basic themes in children''s grief. Firstly, it maintains that children are always developing; therefore their understanding of death and their reactions to illness and loss are also multifaceted and constantly undergoing change. Secondly, children grieve in ways that are both different from and similar to adults. While they may need different therapeutic approaches from their elders, each loss is different and the grief experience will be affected by many of the same factors that affect adults. Thirdly, it holds that they need significant support as they grieve.; Talking to children about loss and and illness is too important to wait until a crisis; rather, it is essential to provide opportunities to discuss loss in times that are not so Emotionally Laden. This Book Aims To Demonstrate That Open Communication between parents and children will lead to skills and understanding that are essential to the child for coping with loss and reaffirming that death is part of the process of living.

Produced as a companion to the Hospice Foundation of America''s fifth annual National Bereavement Teleconference, this volume examines how key aspects of identity affect how individuals grieve. Variables explored include culture, spirituality, age and development level, class and gender.

Produced as a companion to the Hospice Foundation of America''s fifth annual National Bereavement Teleconference, this volume examines how key aspects of identity affect how individuals grieve. Variables explored include culture, spirituality, age and development level, class and gender.

In this “volume of rare sensitivity, penetrating understanding, and profound insights” (Rabbi Earl A. Grollman, author of Living When a Loved One Has Died), Dr. Kenneth Doka explores a new, compassionate way to grieve, explaining that grief is not an illness to get over but an individual and ongoing journey.There is no “one-size-fits-all” way to cope with loss. The vital bonds that we form with those we love in life continue long after death—in very different ways. Grief Is a Journey is the first book to overturn prevailing, often judgmental, ideas about grief and replace them with a hopeful, inclusive, personalized, and research-backed approach. New science and studies behind Dr. Doka’s teaching upend the dominant but incorrect view that grief proceeds by stages. Dr. Doka helps us realize that our experiences following a death are far more individual and much less predictable than the conventional “five stages” model would have us believe. Common patterns of experiencing and expressing grief still prevail, yet many other life changes accompany a primary loss. For example, the deaths of parents, even for adults, modify family patterns, change relationships, and alter old family rituals. Unique to this book, Dr. Doka also explains how to cope with disenfranchised grief—the types of loss that are not so readily recognized or supported by society. These include the death of ex-spouses, as well as non-fatal losses such as divorce, the end of a friendship, job loss, or infertility. In addition, Dr. Doka considers losses that might be stigmatized, including death by suicide or from disease or self-destructive behaviors such as smoking or alcoholism. And finally, Dr. Doka reminds us that, however painful, grief provides opportunities for growth.