Search results for ‘Subject term:"physical disabilities"’ Sort:
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Improving disability services: the way forward for health and social services
- Authors:
- BEGUM Nasa, FLETCHER Sheila
- Publisher:
- King's Fund
- Publication year:
- 1995
- Pagination:
- 32p.,bibliog.
- Place of publication:
- London
Quick guide to improving services for disabled people. Aimed at senior managers in health and social services who may have overall responsibility for services for disabled adults, yet not have a detailed involvement at an operational level. Issues looked at include: information; access; advocacy; assessment; accommodation; aids and adaptations; day care; independence; health care; and user involvement. Also looks at legislation and guidance.
Focus day: services for people with a physical disability; held on 6 July 1992 at the Holiday Inn, Portsmouth
- Author:
- PORTSMOUTH AND SOUTH EAST HAMPSHIRE COMMUNITY HEALTH COUNCIL
- Publisher:
- University of Portsmouth. School of Social and Historical Studies. Social Servic
- Publication year:
- 1993
- Pagination:
- 96p.
- Place of publication:
- Portsmouth
A day of workshops which involved users, carers and service providers. Designed as a practical exercise to obtain the views of users about services.
Assistive technology: independence and well-being
- Author:
- AUDIT COMMISSION
- Publisher:
- Audit Commission
- Publication year:
- 2004
- Pagination:
- 50p.
- Place of publication:
- London
This paper looks in more depth at the role of assistive technology (AT) in supporting independence. It examines the place of AT in the current policy context and describes the current evidence to demonstrate how AT can support independence. It analyses the current obstacles to progress and explains how change can be introduced. New assistive technology can play a vital role in supporting the ways in which millions of older or disabled people can maintain or regain their independence. It also has the potential to modernise the way in which many aspects of health and social care are currently delivered to the benefit of users, carers, service providers and the taxpayer.
Modernising the workhorse: getting the best from service users
- Author:
- SNOW Rose
- Journal article citation:
- MCC Building Knowledge for Integrated Care, 10(4), August 2002, p.26.
- Publisher:
- Pavilion
It is argued that discriminatory attitudes to (ex) service users may threaten modernisation as they limit and shrink the workhorse and prevent committed workers form succeeding. This article summarises the report of the first National Conference of Survivor Workers which gives senior managers the knowledge needed to increase the size and capability of the workhorse.
Involving young people in health service development
- Author:
- SOCIAL POLICY RESEARCH UNIT
- Publisher:
- University of York. Social Policy Research Unit
- Publication year:
- 2002
- Pagination:
- 4p.
- Place of publication:
- York
Summarises research findings from a project to investigate how the NHS consults with chronically ill and disabled young people and to identify factors to support and promote young patients' involvement in service development. The project surveyed 99 health authorities and 410 NHS Trusts in England, and identified 27 projects involving young patients with a chronic illness of physical disability. Data were analysed quantitatively and qualitatively. Six of the projects were examined in greater depth. Discusses levels of involvement; benefits of involvement; and consultation methods.
Developing an interactive approach in social work research: the example of a research study on head injury
- Author:
- HIGHAM P.E.
- Journal article citation:
- British Journal of Social Work, 31(2), April 2001, pp.197-212.
- Publisher:
- Oxford University Press
The paper examines the processes of a research project about the continuing care needs of head-injured people in order to illustrate an interactive approach in social work research. Influenced by the social work values of empowerment and working in partnership, the key function of the interactive approach include a multidisciplinary research team analysing the research topic through different disciplinary perspectives, and selecting research methods and dissemination strategies that promote interactive relationships amongst researchers, respondents and sponsors. Social work practice supplies transferable knowledge, values and skills for the interactive approach. The skill of negotiation is used to mitigate unequal distributions of power between researchers and respondents. The paper concludes that the interactive approach is a distinctive characteristic of social work research that deserves wider recognition.
Disability politics and community care
- Author:
- PRIESTLEY Mark
- Publisher:
- Jessica Kingsley
- Publication year:
- 1999
- Pagination:
- 256p.,bibliog.
- Place of publication:
- London
Addresses the relationship between the politics of disability and community care policies. Argues that although the ideas behind social policy and practice have started to reflect values such as participation, integration and equality, the current policy and its implementation often undermine those goals. Aims to encourage health and social welfare professionals and policy makers to start working with disabled people themselves. Argues that involving disabled people in the design and production of their own welfare will break down the disabling boundary between service provider and user and will result in the reality of integrated living. Presents practical suggestions for change.
Hurtling into a void: transition to adulthood for young disabled people with "complex health and support needs"
- Author:
- MORRIS Jenny
- Publisher:
- Pavilion
- Publication year:
- 1999
- Pagination:
- 159p.,bibliog.
- Place of publication:
- Brighton
Review summarising existing research into health and social services for disabled young people making the transition into adulthood and who have complex health and support needs. Identifies key questions for those commissioning and providing health and social services.
Developing MS healthcare standards: evidence-based recommendations for service providers
- Authors:
- FREEMAN Jenny, et al
- Publisher:
- Multiple Sclerosis Society,|MS Professional Network
- Publication year:
- 2002
- Pagination:
- 37p.
- Place of publication:
- London
The physical and psychosocial problems experienced by people with MS are wide ranging, variable and often complex. This presents problems when defining needs and making recommendations for the provision of high quality services. There are a number of recurring themes throughout this document, reflecting those that are present for people with MS throughout the different stages of the condition. These recommendations provide a clear framework, which should inform the work of all those concerned with MS services including Primary Care Trusts (PCTs), as they lead on consulting with the community and working with social services and other agencies to decide the most effective way of delivering services to people with MS. For practical purposes we considered four phases of the condition: diagnostic; minimal impairment; moderate disability; and severe disability.
Empowerment and advocacy: reflections on action research with Bangladeshi and Pakistani families who have children with severe disabilities
- Authors:
- FAZIL Qulsom, et al
- Journal article citation:
- Health and Social Care in the Community, 12(5), September 2004, pp.389-397.
- Publisher:
- Wiley
The concepts of empowerment and advocacy, and how they impinge on power relationships for service providers working with black and Asian communities, are explored through the findings of a 20-month project carried out between 2000 and 2001 with 19 Pakistani and Bangladeshi families who have children with severe disabilities in Birmingham. This action research project evaluated an advocacy project designed to improve the quality of life for Pakistani and Bangladeshi families with at least one child with severe disabilities. The objectives included improving access to resources, services, information and support in ways which were non-stigmatising, and which were sensitive to the particular needs of the children and their carers. The present paper discusses four main themes: (1) advocacy and empowerment in practice; (2) issues of the efficacy of advocacy and of consultation within advocacy; (3) individual empowerment versus the families' needs; and (4) cultural and gender issues which emerged from the analysis of the study. The authors identify features of empowerment which must be addressed in advocacy services which are sensitive to ethnic differences. These issues must be addressed if services are to reap their potential to make a positive impact on the lives of the most vulnerable and powerless members of the community.