Life to be Lived examines the process of adjustment that patients and their families go through when they face the end of life. Personal research and case-based examples provide a candid look at the challenges from dealing with options from symptom and pain control to adjusting to the psychosocial implications of being ill.
Life to be Lived examines the process of adjustment that patients and their families go through when they face the end of life. Personal research and case-based examples provide a candid look at the challenges from dealing with options from symptom and pain control to adjusting to the psychosocial implications of being ill.
Dr Catherine Proot is a psychology graduate of Ghent University Belgium and holds a counselling diploma and a PhD from the UEA in Norwich. Psychotherapist and clinical supervisor she has specialised in palliative and bereavement care since 2005. She currently works as Psychological Specialist in Palliative Care and Bereavement Coordinator in St Nicholas Hospice Care in Bury St Edmunds, UK. The Very Revd Michael Yorke is a Cambridge graduate in Law and Theology. He also studied at The Tavistock Institute in London and the UEA in Norwich. He is a retired Anglican Priest who worked principally in and through four Cathedrals. He has 45 years of experience as a counsellor and was for 18 years a Samaritan three of which as National Chairman. He is currently Vice Chairman to the Norfolk Hospice near Kings Lynn, UK.
Inhaltsangabe
Part 1: The patient experience 1: The challenge of illness and pain 2: All may not be lost 3: Trials and adjustment 4: Towards a changed outlook Part 2 : The impact on family carers 5: Demands on the family 6: Lives taken over 7: Coping with change 8: Some personal consequences for the carer Part 3: The professional carers and their roles 9: Challenges for the professional carer 10: The power and limitations of words 11: Talking with patients 12: Chaplaincy and spiritual care Part 4: Boundaries and resources 13: Blurred boundaries 14: A wealth of resources Part 5: The next step 15: The next step
Part 1: The patient experience 1: The challenge of illness and pain 2: All may not be lost 3: Trials and adjustment 4: Towards a changed outlook Part 2 : The impact on family carers 5: Demands on the family 6: Lives taken over 7: Coping with change 8: Some personal consequences for the carer Part 3: The professional carers and their roles 9: Challenges for the professional carer 10: The power and limitations of words 11: Talking with patients 12: Chaplaincy and spiritual care Part 4: Boundaries and resources 13: Blurred boundaries 14: A wealth of resources Part 5: The next step 15: The next step
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