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Author: David Clark
Publisher: McGraw-Hill Education (UK)
ISBN: 0335231098
Category : Health & Fitness
Languages : en
Pages : 322
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Book Description
Palliative care is moving through an important period of expansion and development, spreading beyond its original hospice base to encompass care in the community, in hospitals, health centres, clinics and nursing homes. It can now be found in over 70 countries of the world. What challenges does this multidisciplinary speciality face as it seeks to combine high grade pain and symptom control with sensitive psychological, spiritual and social care? What are the implications of current constraints on health policy and planning? How do ethical issues about resource allocation and end of life care impinge? Can palliative care be further extended to include conditions other than cancer? New Themes in Palliative Care addresses these and many related issues in ways which will be readily accessible to students of health and social care as well as to those involved in purchasing or providing palliative care services, and to social scientists interested in chronic illness, death and dying. Its editors are respected experts in the field with backgrounds in the social sciences, nursing and medicine and the book's contributors include leading international figures from a wide range of palliative care and academic disciplines.
Author: David Clark
Publisher: McGraw-Hill Education (UK)
ISBN: 0335231098
Category : Health & Fitness
Languages : en
Pages : 322
Get Book Here
Book Description
Palliative care is moving through an important period of expansion and development, spreading beyond its original hospice base to encompass care in the community, in hospitals, health centres, clinics and nursing homes. It can now be found in over 70 countries of the world. What challenges does this multidisciplinary speciality face as it seeks to combine high grade pain and symptom control with sensitive psychological, spiritual and social care? What are the implications of current constraints on health policy and planning? How do ethical issues about resource allocation and end of life care impinge? Can palliative care be further extended to include conditions other than cancer? New Themes in Palliative Care addresses these and many related issues in ways which will be readily accessible to students of health and social care as well as to those involved in purchasing or providing palliative care services, and to social scientists interested in chronic illness, death and dying. Its editors are respected experts in the field with backgrounds in the social sciences, nursing and medicine and the book's contributors include leading international figures from a wide range of palliative care and academic disciplines.
Author: Julie Ling
Publisher: McGraw-Hill Education (UK)
ISBN: 0335226256
Category : Social Science
Languages : en
Pages : 250
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Book Description
This book describes the history and development of palliative care services in the Republic of Ireland. Written from a multi-professional perspective the book appeals to anyone with an interest in hospice and palliative care in Ireland. In attempting to explore what is different about Irish palliative care, this book delves into the cultural, religious and social factors particular to modern Ireland, from the historical roots of the Irish palliative care movement through to the publication of the Government’s ‘blueprint’ for the future development of services. Palliative Care In Ireland explores the provision of palliative care services, bereavement, the influence of folklore, holistic care, faith, religion and spirituality, and the important contributions of the voluntary sector. The changing face of Ireland is described and challenges ahead are considered. This is the first book to truly capture the Irish dimension and is essential reading for those in emerging services worldwide where similar challenges are faced and where local and national influences determine the uniqueness of a particular model of service delivery. The book is key reading for students and researchers as well as all those involved in the delivery and management of palliative care services. Contributors: Jide Afolabi, Maria Bailey, Frank Brennan, David Clark, Sinéad Donnelly, Matthew Farrelly, Stephen Higgins, Jacqueline Holmes, Kaye Kealy, Michael Kearney, Ann Keating, Orla Keegan, Christy Kenneally, Philip Larkin, Peter Lawlor, Julie Ling, Anna-Marie Lynch, John McCormack, Regina McQuillan, Michael J. Murphy, Tony O'Brien, Eileen O’Leary, Liam O’Síoráin, Maeve O'Reilly, Patrick J Quinlan, Deirdre Rowe, Siobhan Sheehan, Geraldine Tracey, Onja Van Doorslaer, Eithne Walsh.
Author: Pam Firth
Publisher: McGraw-Hill Education (UK)
ISBN: 0335225012
Category : Social Science
Languages : en
Pages : 241
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Book Description
"For anyone seeking to develop their understanding of loss and change, whether in a palliative care of general or social care setting, this book contains much useful material which can be taken selectively or in its entirety." Hospise Information Bulletin How do professionals meet the needs of bereaved people? How do professionals undertake best practice with individuals, groups, families and communities? What are the implications for employing research to influence practice? This book provides a resource for working with a complex range of loss situations and includes chapters on childhood bereavement, and individual and family responses to loss and change. It contains the most up-to-date work in the field presented by experienced practitioners and researchers and is relevant not only for those working in specialist palliative care settings, but for professionals in general health and social care sectors. Strong links are maintained between research and good practice throughout the book. These are reinforced by the coherent integration of international research material and the latest thinking about loss and bereavement. Experts and clinicians draw upon their knowledge and practice, whilst the essential perspective of the service user is central to this book. Loss, Change and Bereavement in Palliative Care provides essential reading for a range of professional health and social care disciplines practising at postgraduate or post-registration/qualification level. It challenges readers, at an advanced level, on issues of loss, change and bereavement. Contributors Lesley Adshead, Jenny Altschuler, Peter Beresford, Grace Christ, Suzy Croft, Pam Firth, Shirley Firth, Richard Harding, Felicity Hearn, Jennie Lester, Gill Luff, Linda Machin, Jan McLaren, David Oliviere, Ann Quinn, Phyllis Silverman, Jean Walker, Karen Wilman.
Author: Simon Dein
Publisher: McGraw-Hill Education (UK)
ISBN: 0335224784
Category : Health & Fitness
Languages : en
Pages : 200
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Book Description
Cancer is more than a biological disease. Cultural factors are involved at every stage in the journey through cancer, from prevention to palliative care. Based upon recent studies from the United Kingdom, Europe and the United States, Culture and Cancer Care examines a number of cultural themes in relation to cancer, including: The disparity of rates of cancer among different ethnic groups Culture and screening Breaking bad news and communication Cultural variations in emotional responses to cancer Cultural variability in cancer treatments and the influence on prognosis Palliative care across cultures The book focuses on three main themes: culture, race and ethnicity and their relationship to cancer; the cultural context of sickness and help-seeking behaviour; the shift from biomedicine to alternative forms of treatment. Throughout the book, a critical stance is adopted towards race and culture, focusing on the relation between these concepts and social deprivation. Culture and Cancer Care is key reading for students, researchers and practitioners in oncology and palliative care, offering a clear analysis of cultural differences with regard to illness and health care, as well as suggestions of how ethnic disparities can be overcome both at a political and local level, through cultural understanding and culturally appropriate health education.
Author: Anne Grinyer
Publisher: McGraw-Hill Education (UK)
ISBN: 0335231667
Category : Health & Fitness
Languages : en
Pages : 210
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Book Description
The original inspiration for this book was George who died from osteosarcoma at the age of 23. During his illness his parents tried without success to access information on the life-stage issues that make life-threatening illness during young adulthood particularly difficult to manage. They could find no literature relating specifically to this problem and struggled throughout George's 4 years of living with cancer to cope with the additional problems faced by families in this situation. After his death they set up a research project to help other families facing these issues. This book is the outcome of that research. It is heavily based on the use of narrative material written by parents whose young adult children have been diagnosed with cancer. The book addresses issues such as sexuality and fertility, independence, the need for normality, the effect on siblings, the ownership of medical information, financial issues, the impact on the parents' partnership and the emotional consequences of the illness. It is designed to be of practical assistance both to parents and to health professionals involved with the care of young adults with cancer.
Author: Simon Woods
Publisher: McGraw-Hill Education (UK)
ISBN: 0335230407
Category : Social Science
Languages : en
Pages : 194
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Book Description
"I enjoyed reading this book very much. It is very readable and well argued using real life cases and thought experiments as well … The book provides the reader with a short history of and an overview of the most important issues in modern palliative care. Various theoretical discussions are clearly set out, such as: the relationship between the hospice movement and modern palliative care, between palliative care and health care in general, between palliative sedation and euthanasia, and the question whether euthanasia can be part of palliative care. The author starts with exploring the existing debates and then develops his own arguments in a balanced and well-structured way." Medicine, Health Care and Philosophy "The text of this book is accessible, the philosophical and ethical arguments are clearly articulated, and relevant ethical principles are integrated into the critique of the issues, making this a very useful book for nurses working in palliative as well as in general care." Nursing Ethics "It is crucially important for any student or researcher who is seriously consideringethical and policy matters at the end of life to embrace and tackle intellectually the issues that Woods raises in this book. I would happily recommend it." Journal of Medical Ethics What constitutes a good death? Is it possible to arrange a good death? Is killing compatible with caring? This book looks at death and the issues and ethical dilemmas faced at the end of life. It addresses the central issues in the field such as: Withholding and withdrawing treatment Euthanasia and assisted suicide Terminal sedation The role of autonomy Palliative care Drawing on a philosophical framework, the author explores end-of-life issues in order to reflect on the nature of the good death and how this may be achieved. The book considers whether it is permissible or desirable to influence the quality of dying: offering palliative sedation as a possible alternative to terminal sedation, the argument is extended to examine why some forms of assisted dying can be shown to be compatible with the ideas of palliative care. Consideration is also given to future developments such as life extension techniques and the ethical questions that that these techniques might raise. As such, the book follows in the ongoing philosophical tradition to critique and analyse current thought on the topic of death, encouraging self-reflection in the reader and offering suggestions for practice in end-of-life care. Death’s Dominion is key reading for students and professionals involved in care of the dying, as well as those with an interest in the philosophical issues surrounding end-of-life care.
Author: Lars Sandman
Publisher: McGraw-Hill Education (UK)
ISBN: 0335227740
Category : Social Science
Languages : en
Pages : 184
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Book Description
·Is there such a thing as a good death? ·Should we be able to choose how we wish to die? ·What are the ethical considerations that surround a good death? The notion of a ‘good death’ plays an important role in modern palliative care and remains a topic for lively debate. Using philosophical methods and theories, this book provides a critical analysis of Western notions surrounding the dying process in the palliative care context. Sandman highlights how our changing ideas about the value of life inevitably shape the concept of a good death. He explores the varying perspectives on the good death that come from friends, family, physicians, spiritual carers and others close to the dying person. Setting out a number of arguments for and against existing thinking about a good death, this book links to the practice of palliative care in several key areas including: ·An exploration of the universal features of dying ·The process of facing death ·Preparation for death ·The environment of dying and death The author concludes that it is difficult to find convincing reasons for any one way to die a good death and argues for a pluralist approach. A Good Death is essential reading for students and professionals with an interest in palliative care and end-of-life issues.
Author: Henk ten Have
Publisher: McGraw-Hill Education (UK)
ISBN: 0335227295
Category : Health & Fitness
Languages : en
Pages : 254
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Book Description
How have Dutch debates on end-of-life care developed so differently from most other countries, finally resulting in the legalization of euthanasia? What are the relevant legal, medical and ethical dimensions of euthanasia and physician assisted suicide? What lessons can be learned from the Dutch experience with euthanasia? In all modern countries a good death and relief of suffering are important issues of public debate. The bioethical debate in the Netherlands is unique since it has been focusing on the issue of euthanasia for more than thirty years. This book describes the debate, explains its origins, and analyses its development, resulting in the legislation of euthanasia. It also presents data on the medical practice of euthanasia with examples of cases. Death and Medical Power details the evolution as well as the complexities of the legal responses to physician involvement in euthanasia. The authors analyze the ethical debate concerning euthanasia, discussing the pros and cons of medical termination of human life. The book concludes with a section on the lessons to be learned from the Dutch experience. This unique study will be of relevance to all clinicians and other professionals involved in end-of-life care, to health policy makers and educators, as well as anybody else interested in the ethics of euthanasia.
Author: Gordon Riches
Publisher: McGraw-Hill Education (UK)
ISBN: 0335232647
Category : Psychology
Languages : en
Pages : 240
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Book Description
* What impact does a child's death have on family relationships? * How might differences in the way mothers and fathers deal with bereavement contribute to increased marital tension? * Why are bereaved siblings so deeply affected by the way their parents grieve? An Intimate Loneliness explores how family members attempt to come to terms with the death of an offspring or brother or sister. Drawing on relevant research and the authors' own experience of working with bereaved parents and siblings, this book examines the importance of social relationships in helping parents and siblings adjust to their bereavement. The chances of making sense of this most distressing loss are influenced by the resilience of the family's surviving relationships, by the availability of wider support networks and by the cultural resources that inform each's perception of death. This book considers the impact of bereavement on self and family identity. In particular, it examines the role of shared remembering in transforming survivors' relationships with the deceased, and in helping rebuild their own identity with a significantly changed family structure. Problems considered include: the failure of intimate relationships, cultural and gender expectations, the invisibility of fathers' and siblings' grief, sudden and 'difficult' deaths, lack of information, and the sense of isolation felt by some family members. This book will be of value to students on courses in counselling, health care, psychology, social policy, pastoral care and education. It will appeal to sociology students with an interest in death, dying and mortality. It is also aimed at professionally qualified counselling, health and social service workers, at informed voluntary group members, the clergy, teachers and others involved with pastoral care.
Author: Mike Nolan
Publisher: McGraw-Hill Education (UK)
ISBN: 0335232434
Category : Medical
Languages : en
Pages : 242
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Book Description
Addressing the needs of older people and their carers is an essential element of both policy and practice in the fields of health and social care. Recent developments promote a partnership and empowerment model, in which the notion of 'person-centred' care figures prominently. However, what 'person-centred' care means and how it can be achieved is far from clear. Working with Older People and their Families combines extensive reviews of specialist literatures with new empirical data in an attempt at a synthesis of themes about making a reality of 'person-centred' care. Uniquely, it seeks to unite the perspectives of older people, family and professional carers in promoting a genuinely holistic approach to the challenges of an ageing society. Working with Older People and their Families is recommended reading for students on health related courses such as nursing, medicine and the therapies. It is also of relevance to students of social work and social gerontology, researchers, managers and policy makers.
