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Too Ill to Talk?
Af: Neil Small, Penny Rhodes Engelsk Paperback
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kr 15
Too Ill to Talk?
Af: Neil Small, Penny Rhodes Engelsk Paperback

User involvement has become an important part of health policy initiatives during the last decade, but how realistic is the concept and do all users want to be involved? This book brings the voices of people with serious illness, and those caring for them, into debate about how far health and social care services can reflect the views of users.

Providing an overview of the literature on user involvement, the book looks at the policy and professional context within which user involvement is undertaken, in particular user involvement in pallative care. The authors discuss two key concepts - palliative care and empowerment - and analyse the role of self-help groups and new information and communication technologies in this context. The book focuses on the detailed narratives of people coping with three life-threatening illnesses - cystic fibrosis, multiple sclerosis and motor neurone disease - and in this way the views and experiences of the ''user'' are brought into play to critique current policy and practice.

Addressing a current health services issue in a refreshingly critical manner the text challenges the assumption that user involvement is either easy to achieve or that it is necessarily welcomed by all parties. It will be valuable reading for students on health studies courses, health professionals and policy makers in health and social care.

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User involvement has become an important part of health policy initiatives during the last decade, but how realistic is the concept and do all users want to be involved? This book brings the voices of people with serious illness, and those caring for them, into debate about how far health and social care services can reflect the views of users.

Providing an overview of the literature on user involvement, the book looks at the policy and professional context within which user involvement is undertaken, in particular user involvement in pallative care. The authors discuss two key concepts - palliative care and empowerment - and analyse the role of self-help groups and new information and communication technologies in this context. The book focuses on the detailed narratives of people coping with three life-threatening illnesses - cystic fibrosis, multiple sclerosis and motor neurone disease - and in this way the views and experiences of the ''user'' are brought into play to critique current policy and practice.

Addressing a current health services issue in a refreshingly critical manner the text challenges the assumption that user involvement is either easy to achieve or that it is necessarily welcomed by all parties. It will be valuable reading for students on health studies courses, health professionals and policy makers in health and social care.

Produktdetaljer
Sprog: Engelsk
Sider: 264
ISBN-13: 9780415233170
Indbinding: Paperback
Udgave:
ISBN-10: 0415233178
Udg. Dato: 30 nov 2000
Længde: 0mm
Bredde: 234mm
Højde: 156mm
Oplagsdato: 30 nov 2000
Forfatter(e): Neil Small, Penny Rhodes
Forfatter(e) Neil Small, Penny Rhodes


Kategori Sociologi: døden og døende


Sprog Engelsk


Indbinding Paperback


Sider 264


Udgave


Længde 0mm


Bredde 234mm


Højde 156mm


Udg. Dato 30 nov 2000


Oplagsdato 30 nov 2000

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