## Abstract This study examined a UK sample of parents caring for their adult offspring with intellectual disabilities, and the factors contributing to their quality of life and experiences of caregiving. Structured interviews were conducted with 62 parents of adults with intellectual disabilities.
Quality of Life Measurement and People with Intellectual Disabilities: a Reply to Cummins
โ Scribed by Chris Hatton; Alastair Ager
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 64 KB
- Volume
- 15
- Category
- Article
- ISSN
- 1360-2322
No coin nor oath required. For personal study only.
โฆ Synopsis
This paper continues an exchange concerning quality of life measurement and people with intellectual disabilities. It addresses the continuing debate concerning three major issues: the utility of measuring subjective wellโbeing in assessing service quality; the validity of quality of life as a construct; and the wider context within which quality of life assessment takes place. Evidence is presented to argue that subjective wellโbeing should not be used to assess service quality, as it is a largely dispositional trait and measures of subjective wellโbeing can only be reliably completed by a minority of people with intellectual disabilities. Some concerns are raised concerning the validity of current measures of quality of life, in terms of combining objective and subjective aspects of quality of life, summing quality of life domains, and the lack of investigation of the โpsychological realityโ of quality of life as a construct. Finally, arguments concerning the potentially unfortunate consequences of adopting a quality of life approach within services are outlined. Such potentially unfortunate consequences are argued not to be caused by malignant motivations on the part of professionals, but to be the result of broader historical and professional processes.
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