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Ready, willing and disabled
- Authors:
- DAONE Liz, SCOTT Ruth
- Publisher:
- SCOPE
- Publication year:
- 2003
- Pagination:
- 64p.
- Place of publication:
- London
Despite the many government schemes aimed at helping disabled people into employment, disabled people are still five times more likely than non-disabled people to be out of work and claiming benefits. The survey aimed to find out how employers and employees really feel about employing and working with disabled people and to see whether people’s attitudes and opinions are influenced by common stereotypes and generalisations about disabled people and their abilities. The survey asked about the recruitment process, the accessibility of business premises, health and safety regulations, the financial implications of employing a disabled person, people’s knowledge of disability issues, the attitudes of staff and customers towards disabled employees and people’s perceptions of disabled people at work.
A poorly understood condition: disability living allowance and people with CFS/ME
- Author:
- HAMMOND Cathie
- Journal article citation:
- Social Policy and Administration, 36(3), June 2002, pp.254-274.
- Publisher:
- Wiley
This paper questions the adequacy of administrative responses to poorly understood disabling conditions in the UK. It examines the administration of the Disability Living Allowance (DLA) to people with chronic fatigue syndrome or myalgic encephalomyelitis (CFS/ME). The history of DLA are outlined, and research evaluating its administration and impact is reviewed. Quantitative data from the DSS are combined with qualitative data obtained from interviews with claimants and non-claimants of DLA with CFS/ME and with benefits advisers. Additional data from a national survey of people with CFS/ME are incorporated into the analysis. The findings show how the adjudication of DLA is particularly problematic in relation to people with CFS/ME. Decisions are likely to be based on inadequate evidence. These and other relevant findings are discussed in the context of the stigma attached to CFS/ME and other poorly understood disabling conditions, and socio-legal research and theory.