Family carers often play a major role in the care of their dying relative and are prone to negative physical, social, financial and psychological outcomes. It is essential that palliative care professionals can provide care to the relative as well as the patient, and this book offers a practical guide to family carer assessment and support.
Family carers often play a major role in the care of their dying relative and are prone to negative physical, social, financial and psychological outcomes. It is essential that palliative care professionals can provide care to the relative as well as the patient, and this book offers a practical guide to family carer assessment and support.
Support for the family is a key component of palliative care practice and philosophy, with both patient and family construed as the 'unit of care'. However, there is not always formal acknowledgement of the importance of the family carer role, or that of friends, neighbours and other non-professional, informal carers. Consequently, health and social care professionals find carer support work particularly challenging. Symptom management, personal care, andadministering of medications are just some of the tasks taken on by this group of non-professionals, and the impact of this role can have negative emotional, physical, financial and social implications on thecare-giver. Furthermore, family carers consistently report unmet needs, and there has been a lack of intervention studies aimed at improving carer support.This book therefore provides an evidence-based, practical guide to enable health and social care professionals to assess and respond to family carer needs. It also explores the wider sociological, policy, and research issues related to family carers and palliative care.
Peter Hudson is associate professor and the Director of the Centre for Palliative Care Education and Research, an academic unit located within St Vincent's Hospital, affiliated with The University of Melbourne (Victoria, Australia). Peter is a member of the Department of Human Services Palliative Care Implementation Advisory Committee (Victoria), Board member of the International Association of Hospice and Palliative Care and co-founder of the InternationalPalliative Care Family Caregiver Research Collaboration. Peter has a significant background in palliative care education and research, and has extensive experience as a palliative care nurse. He leadsseveral competitively funded multi site research studies and has published widely in international journals.Professor Sheila Payne is an applied social scientist with a background in nursing. Over the last twenty years she has been involved in leading and contributing to research and teaching about research methods in palliative care. She has a special interest in end-of-life care for older people, family caregivers and bereavement support. She holds the Help the Hospices Chair in Hospice Studies based at the International Observatory on End of Life Care at Lancaster University, UK. She alsoco-directs a large five year programme of collaborative research and development called the Cancer Experiences Collaborative. She has published widely in academic and professional journals, and is alsoCo-director of the Cancer Experiences Collaborative, and Vice President European Association of Palliative Care.
Support for the family is a key component of palliative care practice and philosophy, with both patient and family construed as the 'unit of care'. However, there is not always formal acknowledgement of the importance of the family carer role, or that of friends, neighbours and other non-professional, informal carers. Consequently, health and social care professionals find carer support work particularly challenging. Symptom management, personal care, and administering of medications are just some of the tasks taken on by this group of non-professionals, and the impact of this role can have negative emotional, physical, financial and social implications on the care-giver. Furthermore, family carers consistently report unmet needs, and there has been a lack of intervention studies aimed at improving carer support.This book therefore provides an evidence-based, practical guide to enable health and social care professionals to assess and respond to family carer needs. It also explores the wider sociological, policy, and research issues related to family carers and palliative care.
This item is eligible for free returns within 30 days of delivery. See our returns policy for further details.