Chronic and Terminal Illness
New perspectives on caring and carers
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10% KEDVEZMÉNY?
- A kedvezmény csak az 'Értesítés a kedvenc témákról' hírlevelünk címzettjeinek rendeléseire érvényes.
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32 508 Ft (30 960 Ft + 5% áfa)
Az ár azért becsült, mert a rendelés pillanatában nem lehet pontosan tudni, hogy a beérkezéskor milyen lesz a forint árfolyama az adott termék eredeti devizájához képest. Ha a forint romlana, kissé többet, ha javulna, kissé kevesebbet kell majd fizetnie.
- Kedvezmény(ek) 10% (cc. 3 251 Ft off)
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Iratkozzon fel most és részesüljön kedvezőbb árainkból!
Feliratkozom
32 508 Ft
Beszerezhetőség
Megrendelésre a kiadó utánnyomja a könyvet. Rendelhető, de a szokásosnál kicsit lassabban érkezik meg.
Why don't you give exact delivery time?
A beszerzés időigényét az eddigi tapasztalatokra alapozva adjuk meg. Azért becsült, mert a terméket külföldről hozzuk be, így a kiadó kiszolgálásának pillanatnyi gyorsaságától is függ. A megadottnál gyorsabb és lassabb szállítás is elképzelhető, de mindent megteszünk, hogy Ön a lehető leghamarabb jusson hozzá a termékhez.
A termék adatai:
- Kiadó OUP Oxford
- Megjelenés dátuma 2001. május 17.
- ISBN 9780192631671
- Kötéstípus Puhakötés
- Terjedelem180 oldal
- Méret 235x156x11 mm
- Súly 274 g
- Nyelv angol 0
Kategóriák
Rövid leírás:
This edited book provides a critique of the theoretical concepts of caring, carers and caregivers, based on empirical evidence from recent studies with adults with acquired chronic illnesses, including terminal illness.
TöbbHosszú leírás:
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.
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.
Tartalomjegyzék:
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