Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.523883
Title: Young adults and disability : transition to independent living?
Author: Hendey, Nicola
Awarding Body: University of Nottingham
Current Institution: University of Nottingham
Date of Award: 1999
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Abstract:
The study aims to explore young disabled peoples I concerns about independent living, and how they view the source of that independence. The transition to adulthood poses particular problems for young physically disabled adults and independent living is a widely shared goal. The independent living movement has spearheaded an increasing awareness amongst disabled people of their rights as human beings and citizens and has brought together ideas on independent living and ways of achieving it. The philosophy of independent living is based on four assumptions: that all human life is of value; that anyone, regardless of their impairment, is capable of exerting choices; that people who are disabled by society's reaction to physical, intellectual and sensory impairment and to emotional distress have a right to have control over their lives, with whatever assistance they need to do so; and that disabled people have the right to participate fully in society. Government policy is consonant with the aims of the independent living movement: to keep individuals in the community and to address their needs more appropriately. This study, which is based upon data from 42 young physically disabled adults uses qualitative methods which were inspired by the ideals of the Emancipatory Research Paradigm. Interviews were in-depth and informal and focussed on the periods before, during, and after transition. The work was conducted from the standpoint of the seven fundamental needs outlined in the social model of disability. To what extent had the young people achieved independent living? None of the sample had achieved independent living in its fullest sense in terms of employment, independent housing, financial and personal control of assistance, life style, relationships, educational qualifications or transport. A minority had achieved some of these. The majority had low self-esteem and had received inadequate support from families and the education system and had poor employment prospects. Most were reliant on benefits which were insufficient to meet the extra costs associated with disability and few had received support from social services. Most appeared destined for a life on the margins of society.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.523883  DOI: Not available
Keywords: HV Social pathology. Social and public welfare
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