By Barbara Monroe, David Oliviere
ISBN-10: 0198515812
ISBN-13: 9780198515814
ISBN-10: 1423701119
ISBN-13: 9781423701118
Constructing an inventive alliance with the 'person' past the 'patient' is a center guideline of powerful palliative care. the necessity for a greater knowing of the way to increase lively partnerships among provider clients and execs hasn't ever been larger. This publication examines growth to date and attemts to delineate destiny demanding situations through bringing jointly a number one team of physicians, nurses, social employees, chaplains and psychologists who rigidity the significance of sufferer participation in palliative care.Recent advancements are coated in addition to bereavement matters and cultural changes. there's additionally fabric from the sufferers themselves. most significantly, this ebook highlights the problems in related to sufferers of their personal care as a result of bad lifestyles expectancy, debilitating affliction and serious ache. extra wisdom and perception is required to work out how a ways those sufferers can realistically be anticipated to be excited by enhancing the companies they need.The publication should be of curiosity to a multi-professional viewers in palliative care quite practitioners normally and expert palliative care, expert nurses, bereavement counsellors, and social staff. viewers
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Extra info for Patient Participation in Palliative Care: A Voice for the Voiceless
Example text
National Council for Hospice and Specialist Palliative Care Services (2002) Patients and carers take part in developing services. Information Exchange, Number 35, May, pp. 12–13. Small N and Rhodes P (2000) Too Ill To Talk: User Involvement in Palliative Care. London: Routledge. Thomas K (2001) The Gold Standards Framework Project for Community Palliative Care Home Pack: Information for Patients and Carers. London: Macmillan Cancer Relief and the NHS Modernisation Agency. Wann M (1995) Building Social Capital: Self Help in the Twenty-First Century Welfare State.
Key issues that emerged included the importance of maximizing people’s control over their lives, of self-help and support groups and of meaningful involvement rather than tokenism. Participants wanted more opportunities for meeting together and a national group has now been set up (Beresford et al. 2000b). 33 34 DEVELOPMENTS IN USER ORGANIZATIONS St Christopher’s Hospice At St Christopher’s Hospice, two user groups have been successfully set up, one for ward-based patients and one for those living at home.
The views given by patient and carer can also be used to improve services for others. The pack is written in accessible language and clearly set out and enables the individual user to be involved in improving care both for themselves and others (Thomas 2001). This kind of approach confers direct benefit to the individual while also collecting information about user need more generally. Conclusion User organizations play an important role in enabling people to have a voice. Sharing their experience and issues as a peer group can confer confidence and a shared identity and build knowledge.
Patient Participation in Palliative Care: A Voice for the Voiceless by Barbara Monroe, David Oliviere
by David
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