Unshared Care


Book Description

The vast majority of the 100,000 or so children with serious mental or physical disabilities in Britain today live at home with their families. A series of in-depth interviews carried out with a number of parents enabled the author to describe the extensive physical, practical and emotional demands made on those looking after their disabled child at home. In their own words, parents report how and when they learnt about their child's disability; the sheer physical work and mental effort of daily care which more often than not fall unremittingly on the child's mother; the feelings of isolation and the lack of information which are often relieved only by talking with parents of other disabled children. Unshared Care examines the community services available, revealing that, from the parents' point of view, the rhetoric of public concern is only barely matched by the practical support available. It shows that services are, all too often, insufficiently specialized and lacking in coherence.




Parents as Care Managers


Book Description

First published in 1999, this volume examines the inclusion of disabled children as a category of children in need under the Children Act 1989 and as eligible for assessments of need under the NHS and Community Care Act 1990 has drawn renewed attention to the plight of these children and their families. This book presents the findings from a study of parents whose child has cerebral palsy. The research undertaken at the cost of social policy change focuses on the apparent gap between the well-argued proposals for community care and the experiences of carers. A bewildering picture emerges of inadequate services and treatments from the health, education and social services in the public, voluntary and private sectors. Parents experience isolation and stress as they explore ways to improve the quality of their children’s lives by experimenting with unregulated and under-researched treatments for an incurable physical condition. The conclusion that there has been deterioration in provision for these families is a serious indictment on current social policy direction.




Lone Mothers Between Paid Work and Care


Book Description

This title was first published in 2000. This is a study which compares and contrasts how lone mothers' relationships to paid work and care-giving are constructed across 20 countries, and with what outcomes for lone mothers' levels of economic well-being. In doing so, the book explores from an international perspective, the implications of the re-orientation of lone mothers' citizenship within the UK policy field from that of care-giver to paid worker. The volume engages with feminist comparative social policy literature concerned with specifying a construction of citizenship appropriate to capturing international variations in women's social rights. By incorporating social rights attached to paid work and care, as well as those which enable lone mothers to move between sequential periods of paid work and care-giving across the child-rearing cycle, the study makes a significant contribution to the literature.




Caring and Competent Caregivers


Book Description

Chronic health conditions are the leading cause of illness, disability, and death in the United States today, affecting nearly one hundred million citizens. These conditions cost the economy more than $470 billion a year in direct medical costs, and more than $230 billion in lost productivity. While Americans pride themselves on living in a caring country, society as a whole has not fully prepared for the many challenges presented by chronic illness. This timely book illustrates the caregiving needs to be faced in the next century. Written by individuals associated with the National Quality Caregiving Coalition (NQCC) of the Rosalynn Carter Institute, Caring and Competent Caregivers is a foundation book for use by academicians conducting professional training programs, diverse health care and social service providers on the front lines providing assistance to others, and students entering the field. Incorporating philosophy, social science research, and impressionistic evidence, this book provides a basis for education and practice that is both inspirational and practical.




Imagistic Care


Book Description

Imagistic Care explores ethnographically how images function in our concepts, our writing, our fieldwork, and our lives. With contributions from anthropologists, philosophers and an artist, the volume asks: How can imagistic inquiries help us understand the complex entanglements of self and other, dependence and independency, frailty and charisma, notions of good and bad aging, and norms and practices of care in old age? And how can imagistic inquiries offer grounds for critique? Cutting between ethnography, phenomenology and art, this volume offers a powerful contribution to understandings of growing old. The images created in words and drawings are used to complicate rather than simplify the world. The contributors advance an understanding of care, and of aging itself, marked by alterity, spectral presences and uncertainty. Contributors: Rasmus Dyring, Harmandeep Kaur Gill, Lone Grøn, Maria Louw, Cheryl Mattingly, Lotte Meinert, Maria Speyer, Helle S. Wentzer, Susan Reynolds Whyte




Routledge Handbook of Cultural Gerontology


Book Description

Later years are changing under the impact of demographic, social and cultural shifts. No longer confined to the sphere of social welfare, they are now studied within a wider cultural framework that encompasses new experiences and new modes of being. Drawing on influences from the arts and humanities, and deploying diverse methodologies – visual, literary, spatial – and theoretical perspectives Cultural Gerontology has brought new aspects of later life into view. This major new publication draws together these currents including: Theory and Methods; Embodiment; Identities and Social Relationships; Consumption and Leisure; and Time and Space. Based on specially commissioned chapters by leading international authors, the Routledge Handbook of Cultural Gerontology will provide concise authoritative reviews of the key debates and themes shaping this exciting new field.




Disabled Children


Book Description

This volume of essays attempts to identify the shared experiences of disabled children and examine the key debates about their care and control. The essays follow a chronological progression while focusing on the practices in a number of different countries.




The Costs of Caring


Book Description

First published in 1985, this book considers the financial consequences of parents and other relatives caring for severely disabled children at home. At the time of publication little reliable information was available on the costs incurred by ‘informal carers’, which this book set to rectify. The volume interweaves hard statistical material about money with the detailed personal responses of parents. It examines the claim that disablement in a child reduces parents’ earnings while simultaneously creating an extra expense. The author compares the incomes and expenditure patterns of more than 500 families with disabled children and 700 control families of the time showing that the financial effects of disablement in a child can be far-reaching and pervasive. This book discusses contemporary policy implications of these findings in a chapter dealing with the rational for compensating families with disabled children, and in the final chapter. Although the book was original published in 1985, it references issues that are still important today and, whilst its main concern is families with disabled children, it will also be useful to anyone caring for other kinds of dependent people, such as the elderly.




Half a Century of British Politics


Book Description

Leading experts assess the past fifty years of British political life. Retreat from empire to Europe, with all the adjustments this entailed, is explored, as is the changing nature of politics at home.