Grieving Beyond Gender: Understanding the Ways Men and Women Mourn is a revision of Men Don't Cry, Women Do: Transcending Gender Stereotypes of Grief. In this work, Doka and Martin elaborate on their conceptual model of "styles or patterns of grieving" - a model that has generated both research and acceptance since the publication of the first edition in 1999. In that book, as well as in this revision, Doka and Martin explore the different ways that individuals grieve, noting that gender is only one factor that affects an individual's style or pattern of grief. The book differentiates intuitive grievers, where the pattern is more affective, from instrumental grievers, who grieve in a more cognitive and behavioral way, while noting other patterns that might be more blended or dissonant. The model is firmly grounded in social science theory and research. A particular strength of the work is the emphasis placed on the clinical implications of the model on the ways that different types of grievers might best be supported through individual counseling or group support.

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.

""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 Journal

"With 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, PhD
University of Memphis

"This 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

Aging Education provides educators in aging studies with a unique text that responds to the paucity of instructional strategies and teaching materials. Editors Nieli Langer and Terry Tirrito meet the challenge of educating and training students and providers of service to an aging population in all the various instructional programs (gerontology/geriatrics degrees) and non-credit workshops currently offered in different settings (hospitals, nursing homes, professional associations, in-service training, etc). By developing and explaining a multidisciplinary approach to working with older adults in areas related to health, education, ethics, law, cultural competency for a multicultural population, translating social policy into practice, spirituality, and human services, the editors provide an imaginative and thought-provoking unmet need for gerontology educators by providing them with teaching and practice strategies in aging education.

This work 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. It 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.

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.

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.

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.

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 1995. Routledge is an imprint of Taylor & Francis, an informa company.

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

Grieving Beyond Gender: Understanding the Ways Men and Women Mourn is a revision of Men Don't Cry, Women Do: Transcending Gender Stereotypes of Grief. In this work, Doka and Martin elaborate on their conceptual model of "styles or patterns of grieving" -- a model that has generated both research and acceptance since the publication of the first edition in 1999. In that book, as well as in this revision, Doka and Martin explore the different ways that individuals grieve, noting that gender is only one factor that affects an individual's style or pattern of grief. The book differentiates intuitive grievers, where the pattern is more affective, from instrumental grievers, who grieve in a more cognitive and behavioral way, while noting other patterns that might be more blended or dissonant. The model is firmly grounded in social science theory and research. A particular strength of the work is the emphasis placed on the clinical implications of the model on the ways that different types of grievers might best be supported through individual counseling or group support.

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.

Contents:
Part 1 The Child's Perspective of Death: Children's Understandings of Death - Striving to Understand Death; Grieving Children: Can We Answer Their Questions. Part 2 The Child's Response to Life-Threatening Illness: Talking to Children About Illness; The Child and Life-Threatening Illness; Children and HIV: Orphans and Victims. Part 3 Children Mourning, Mourning Children: Grief of Children and Parents; Children and Traumatic Loss; How Can We Help; The Role of School. Part 4 Innovative Research: World of Dying Children and Their Well Siblings; The Empty Space Phenomenon: The Process of Grief in the Bereaved Family; A Sampler of Literature for Young Readers: Death, Dying and Bereavement.

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 s