Overview

Society has become increasingly diverse; multi-cultural, multi-faith and wide ranging in family structures. The wealthier are healthier and social inequalities are more pronounced. Respecting and working with the range of 'differences' among service users, families and communities in healthand social care with ill, dying and bereaved people is a neglected area in the literature. As the principles of palliative and end of life care increasingly permeate the mainstream of health and social care services, it is important that professionals are sensitive and respond to the differingneeds of individuals from diverse socio-economic backgrounds, ethnicities, beliefs, abilities and sexual orientations, as well as to the different contexts and social environments in which people live and die.This book explores what underpins inequality, disadvantage and injustice in access to good end of life care. Increasingly clinicians, policy planners, and academics are concerned about inequity in service provision. Internationally, there is an increasing focus and sense of urgency both ondelivering good care in all settings regardless of diagnosis, and on better meeting the needs of vulnerable and disadvantaged groups.National initiatives emphasise the importance of resolving disparities in care and harnessing empowered user voices to drive change. This newly expanded, fully revised second edition, with 11 new chapters, provides a comprehensive analysis of discrimination, difference and disadvantage in end oflife care, and offers practical guidance for all who seek to support the equitable provision of good end of life care.

ISBN-13

9780199599295

ISBN-10

0199599297

Weight

0.82 Pounds

Dimensions

9.10 x 0.60 x 6.10 In

List Price

$81.00

Edition

2nd Edition

Format

Paperback

Language

English

Pages

240 pages

Publisher

Oxford University Press

Published On

2012-02-20



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