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Offering practical suggestions for humane caregiving, this valuable new book is aimed at all providers of medical care. This compassionate volume focuses on the development of the thanatology curriculum--teaching caregivers who are just beginning their professional lives to be adequately prepared to deal appropriately with dying patients and their families and to cope with the personal toll exacted by this aspect of medical practice. At a time when increasingly complex medical technology promotes more impersonal contact between caregivers and patients, the contributors emphasize the importance of providing compassionate, responsive, and humane care to those whose lives are ending.
If ever there was an area requiring that the research-practice gap be bridged, surely it occurs where thanatologists engage with people dealing with human mortality and loss. The field of thanatology—the study of death and dying—is a complex, multidisciplinary area that encompases the range of human experiences, emotions, expectations, and realities. The Handbook of Thanatology is the most authoritative volume in the field, providing a single source of up-to-date scholarship, research, and practice implications. The handbook is the recommended resource for preparation for the prestigious certificate in thanatology (CT) and fellow in thanatology (FT) credentials, which are administered and granted by ADEC.
The third edition of the Handbook of Thanatology is an accessible volume that offers essential knowledge in the field of thanatology in a format that is practical for both novices and those with extensive experience in the field. The Association for Death Education and Counseling (ADEC) is an international and professional organization "dedicated to promoting excellence and recognizing diversity in death education, care of the dying, grief counseling and research in thanatology." A key aim of the organization is "to advance the body of knowledge and to promote practical applications of research and theory." While providing resources and support to its multidisciplinary membership, ADEC strives to educate the broader public and to enact its vision of "a world in which dying, death, and bereavement are recognized as fundamental and significant aspects of the human experience" The editors actively recruited fifty-four authors from fourteen countries who represented diversity with regard to disciplines (e.g., nursing, social work. medicine, psychology) and demographics (e.g., gender, citizenship, and race/ethnicity). They intentionally engaged authors from different countries for each chapter, and in most cases, met this goal. As a result, readers will find many useful points of cultural comparison throughout the volume. Some author pairings represent scholars previously unknown to each other and the substance of their joint contributions has emerged as unique, dynamic, and exciting. The Handbook provides important background information on specific topics within the field while also addressing controversies related to them. Initial chapters emphasize foundational topics including definitions of death, death-related attitudes, the epidemiology and demography of death, end-of-life care, and memorialization. The middle chapters focus on grief theories, distinct conceptualizations and considerations of grief based on cause of death, and problematic grief. The volume concludes with chapters highlighting the broad topics of death education, professional practice, history of the field, social presentations of death, and non-death losses.
`This second edition, which has also been edited by Samson Katz, utilizes around half of the original text, of which a significant portions has been revised and updated. The remainder comprises new material reflecting both the changes in attitudes generally towards death and dying, and also designed to meet the needs of students undertaking the revised curriculum of the K260. This book will stimulate thinking and challenge the personal views of both academics and those in practice. ...[A] valuable tool for both those new to the area of palliative and cancer care and those experienced professionals searching for a new angle on several key topics in relation to ethical issues occurring in this speciality... [A]n excellent balance of theoretical contents and moving prose... [T]his book is directed towards all professionals working in health and social care. ...This book is a must for pre-registration students wishing to gain greater understanding of the psychosocial issues faced by those with a terminal illness and their significant others' - Nurse Education Today The fully revised and updated edition of this bestselling collection combines academic research with professional and personal reflections. Death, Dying and Bereavement addresses both the practical and the more metaphysical aspects of death. Topics such as new methods of pain relief, guidelines for breaking bad news, and current attitudes to euthanasia are considered, while the mystery of death and its wider implications are also explored. A highly distinctive interdisciplinary approach is adopted, including perspectives from literature, theology, sociology and psychology. There are wide-ranging contributions from those who come into professional contact with death and bereavement - doctors, nurses, social workers and councellors. In addition there are more intimate personal accounts from carers and from bereaved people. Death, Dying and Bereavement is the Course Reader for The Open University course Death and Dying, which is offered as part of The Open University Dilpoma in Health and Social Welfare. Praise for the First Edition: `The book does give a broad overview of many of the issues around death, dying and bereavement. It raises the reader's awareness and encourages deeper investigation at every level. It is easy to reda and therefore accessible to a wide audience' - Changes `Provides a richly woven tapestry of personal, professional and literary accounts of death, dying and bereavement' - Health Psychology Update `Offers a unique collection of fascinating information, research, stories, poems and personal reflections. It is unusual to experience such a diversity of writings in one book' - Nursing Times `It brings together the knowledge and skills from a multi-occupational group and thereby offers and opportunity, to whoever reads it, to enable better experiences for those who are dying and bereaved' - Journal of Interprofessional Care `For those trying to help the dying and bereaved, this volume will inspire and move you as much as it will inform and guide your work' - Bereavement Care `Provides a unique overview, and in many areas, penetrating insights into various aspects of death, dying and bereavement. One of it's major strengths is that it brings together a wide and varied discourse on death across cultures and through time' - British Journal of Sociology
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.