This book draws on recent research and cutting-edge ideas about bereavement and carers’ experiences across the life course to explore carers’ experience of loss and discuss their specific needs prior and or following the death of those they care for.
Whether care provided is related to a long term or life limiting condition, many carers experience a multitude of losses including indefinite loss characterised by the loss of a taken-for-granted future, and an inability to plan for the future. Carers may also experience anticipatory grief as multiple losses such as companionship, personal freedom, and control manifest. While many carers are dedicated and committed to their role, they are subject to burnout and disenfranchised grief. When the role of caregiver ends as a result of the death of those cared for, this can represent a major change and a period of significant adjustment for carers leading to a range of emotions experienced.
This book presents and discusses research findings, practitioner perspectives, and a wealth of personal accounts to illuminate this vital but neglected area and extend our understanding of loss for carers across the life course. This interdisciplinary and interprofessional volume brings together authors from a wide range of backgrounds, including carers themselves. It is an important contribution to the burgeoning literature around the role and experiences of carers and will interest academics, students and practitioners in health and social care, counselling, and psychology with an interest in loss and bereavement.
This book draws on recent research and cutting-edge ideas about bereavement and carers’ experiences across the life course to explore carers’ experience of loss and discuss their specific needs prior and or following the death of those they care for.
List of figures and tables
List of contributors
Introduction
1: Ambiguous loss: Personal and professional reflections
2: Impact on identity for those working as healthcare professionals when
taking on the role of carer
3: I could cry all day, every day, about my losses: Caring for young adults
with life-shortening conditions families experiences of disruption and
loss
4: From physically active to physically inactive: Understanding the
experiences of a familial carers loss of self
5: Both sides of the coin: A mothers experience of caring for an adult
daughter living with serious life-limiting illness
6: God hasnt given up on them: Christian dementia carers narratives of
experiencing and challenging anticipatory grief and social death
7: The grief of care partners of people living and dying with dementia: A
psychodynamic perspective
8: When an adult with significant caregiving responsibilities for children is
at end-of-life with cancer: A carers pre-bereavement and post-bereavement
experiences
9: When caring ends: Exploring the hidden aspects of loss in trajectories out
of caring in Australia
10: Former carers: Grief, loss and other stories
Index
Kerry Jones is a Senior Lecturer at The Open University, UK, where her research and teaching focus on death, dying, grief, bereavement and end-of-life care. As Co-Lead of the Open University Carers Research Group, she has published and presented her research on care homes and care-giving staff during the pandemic, stillbirth neonatal death, parental bereavement, brain injury, dementia and suicide. Kerry was an academic consultant for A Time to Live on BBC 2.
Joanna Horne is a Senior Lecturer in Psychology and Counselling at The Open University, UK. She conducts research within the areas of physical activity and carer wellbeing, and support needs of young carers. Jo is a member of the Open University Carers Research Group.
