Abstract
Respite aims to alleviate the stress and burden of caring for someone with an intellectual disability and/or autism. Respite can take place in a number of different ways, but most commonly occurs in a residential setting. Based on survey and interview data with carers (CAs), service users and stakeholders (STs) in a northern city in England, this article explores some of the perceived or actual barriers to availing 'non-residential' respite. A number of barriers to non-residential respite are identified. Residential respite appears to be the default conceptualization of 'respite' for carers, service users and stakeholders. Persuading carers, service users and stakeholders to give up the familiarity and safety of residential respite in favour of a non-residential alternative will be challenging unless those involved are more informed. Limitations and directions for future research are suggested.
More Information
Identification Number: | https://doi.org/10.1177/1744629516658577 |
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Status: | Published |
Refereed: | Yes |
Publisher: | Sage |
Uncontrolled Keywords: | carers, residential care, respite, support services, Rehabilitation, 1110 Nursing, 1303 Specialist Studies In Education, |
Depositing User (symplectic) | Deposited by Southby, Kris |
Date Deposited: | 19 Aug 2016 14:49 |
Last Modified: | 11 Jul 2024 04:52 |
Item Type: | Article |
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Note: this is the author's final manuscript and may differ from the published version which should be used for citation purposes.
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