This book draws together the learning of a wide range of social workers and other professionals engaged in end of life care who recognise that dying is essentially a social experience and want to tailor a personal, professional and societal response accordingly. Through a systemic lens, the book explores the nature and experience of living and dying in the UK today, then considers ways in which social workers and others may want to work with people who are affected by a diagnosis of a life-threatening condition. The contributors offer rich and contemporary perspectives on death, dying and loss, reflective of their different approaches and interests. The insights of the book are timely, given the growing levels and changing nature of needs for people who are coming to the end of their life in the UK and beyond, and the related requirements for compassionate, personalised and holistic care within the increasingly professionalised arena of health and social care. This book will be of interest to social work practitioners, students, and others committed to psychosocial support of people who are dying or bereaved, and who want to consider how to provide this support most effectively. Professionals who are interested in working alongside social workers to deliver high quality end of life care will also find this publication useful. This book was originally published as a special issue of the Journal of Social Work Practice.
The first text to explore the history, characteristics, and challenges of hospice social work, this volume weaves leading research into an underlying framework for practice and care.
This book is a useful tool for any social worker working with individuals and families navigating complex health care systems.
Social workers from diverse settings will benefit from its international scope and wealth of patient and family narratives. Unique to this scholarly text is its emphasis on the collaborative nature inherent in palliative care.
This book is a useful tool for educators, learners, and practicing social workers working with individuals and families navigating complex health care systems.
Instead of offering easy solutions, this book provides detailed accounts that provoke stimulating debates among students, enabling them to confront their own responses, beliefs, and uncertainties to hone their critical thinking and decision ...
Turner, M. and Beresford, P. (2005) User Controlled Research: Its Meanings and Potential, Final Report. ... White, I., Devenney, M., Bhaduri, R., Barnes, M., Beresford, P. and Jones, A. (1988) Hearing the Voice of the Consumer.
Those entering the social work field will find this an indispensible guide as they select their specialty and begin their career.
Improving Palliative Care for Cancer examines the barriersâ€"scientific, policy, and socialâ€"that keep those in need from getting good palliative care.
This book supports these needs by providing a comprehensive approach to nursing practice in fragility fracture care.
Organized around theoretical issues in loss, grief, and bereavement, and around clinical practice with individuals, families, and groups, the book addresses practice with people who have specific illnesses such as AIDS, bone marrow disease, ...