Chronic and Terminal Illness

New perspectives on caring and carers

Häftad, Engelska, 2001

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Beskrivning

Most chronically and terminally ill patients are cared for in their own homes by family and friends, rather than in hospitals or hospices. These carers are an invaluable free resource and there is an increasing amount of research into their role and the experiences in caring for the terminally ill, patients with cancer and patients with other chronic diseases. This book provides a critique of the theoretical concept of caring, carers and caregivers. Material is based on empirical evidence from recent studies with adults with acquired chronic illnesses, including terminal illness. The empirical data within the book has been gathered from the perspective of those providing personal, domestic or emotional care to others already known to them by virtue of kinship, co-habitation or friendship, rather than carers organised on a professional or voluntary basis. This new evidence is used to make suggestions about possible ways forward within health and social care practice. Students in the fields of health and social care as well as in social sciences undertaking courses with a health focus, practitioners and researchers in palliative care and all those involved in health services provision for the chronically ill will find this book extremely valuable.

Produktinformation

Utgivningsdatum:2001-05-17
Mått:156 x 235 x 11 mm
Vikt:274 g
Format:Häftad
Språk:Engelska
Antal sidor:180
Förlag:OUP OXFORD
ISBN:9780192631671

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Recensioner i media

This is a very welcome text that examines informal caring from a holistic perspective, exploring the emotional and social implications of caring and the impact of societal and professional attitudes on carers. Theoretical perspectives and research findings are integrated well, supported by plentiful examples of real life experiences. It includes a good mix of studies and each chapter is well referenced for readers who wish to explore particular aspects in more depth... The content is informative, refreshing and challenging to existing attitudes to carers and includes helpful suggestions for practice. I would certainly recommend it to students on palliative care courses and encourage teachers to give carers more voice in their courses by using it as a key text.

Innehållsförteckning

Being a carer ; Positive aspects of caring ; Caring and identity: the experience of spouses in stroke and other chronic neurological conditions ; A longitudinal study of carers providing palliative care ; Who is a carer? Experiences of family caregivers in palliative care ; Being a carer in acute crisis: the situation for relatives of organ donors ; Family Caregiving: A Gender-Based Analysis of Women's Experiences ; The Contribution of Carers to Professional Education ; The future: interventions and conceptual issues