Death, dying, and social differences
Author(s)
Bibliographic Information
Death, dying, and social differences
Oxford University Press, 2004
- : pbk
Available at 5 libraries
  Aomori
  Iwate
  Miyagi
  Akita
  Yamagata
  Fukushima
  Ibaraki
  Tochigi
  Gunma
  Saitama
  Chiba
  Tokyo
  Kanagawa
  Niigata
  Toyama
  Ishikawa
  Fukui
  Yamanashi
  Nagano
  Gifu
  Shizuoka
  Aichi
  Mie
  Shiga
  Kyoto
  Osaka
  Hyogo
  Nara
  Wakayama
  Tottori
  Shimane
  Okayama
  Hiroshima
  Yamaguchi
  Tokushima
  Kagawa
  Ehime
  Kochi
  Fukuoka
  Saga
  Nagasaki
  Kumamoto
  Oita
  Miyazaki
  Kagoshima
  Okinawa
  Korea
  China
  Thailand
  United Kingdom
  Germany
  Switzerland
  France
  Belgium
  Netherlands
  Sweden
  Norway
  United States of America
Description and Table of Contents
Description
"Death, Dying and Social Differences" addresses the importance of care of dying people in their social context. It focuses on the much neglected area of the social aspects of death and dying. It highlights the key ways that health and social care professionals who provide end of life care can cater for those from a variety of social circumstances and communities. It speaks about best professional practice that can balance the inequalities in society's structures and what that means for the dying and their carers. A first of its kind, the twelve chapters by leaders in their fields, are aimed at clinicians and practitioners from all disciplines, policy-makers and managers who are committed to palliative and good end of life care for all. A multi-professional and case-based approach underpins the principles and practices of innovative care.
The book considers the differences in the palliative care of people with advanced cancer and other life threatening conditions, related to poverty, social class, gender, sexuality, age, ethnicity and religion, as well as the circumstances of patients and carers who have disabilities, experience psychiatric illness, are refugees, are subject to abuse or who are prisoners. It uncovers 'disadvantaged dying' and suggests appropriate responses. The physical, spiritual, psychological and holistic aspects of care are largely shaped by and intertwined with a person's environment and social experiences. The book unpacks this essential ingredient of care of the very ill and bereaved and those close to them. Although death can be a great leveller, it can also highlight great differences in the quality of the experience. This book offers a key to upholding maximum human dignity for dying people and those they leave behind.
Table of Contents
- Foreword
- 1. Introduction: working with death, dying and difference
- 2. Social class, poverty and social exclusion
- 3. Minority ethnic communities and religious groups
- 4. Sexual identity - gender and sexual orientation
- 5. Older people
- 6. Mental health needs
- 7. Disability
- 8. Abuse
- 9. Offenders
- 10. Refugees
- 11. Finances
- 12. Carers and caregivers
by "Nielsen BookData"