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Contrasting perspectives of parents and service providers on respite care in Queensland, Australia
Journal article   Open access   Peer reviewed

Contrasting perspectives of parents and service providers on respite care in Queensland, Australia

Cynthia Teo, Ann Kennedy-Behr and John B Lowe
Disability & Society, Vol.33(9), pp.1503-1527
2018
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PDF - Author Accepted Version327.16 kBDownloadView
Accepted VersionPDF - Author Accepted Version Open Access
url
https://doi.org/10.1080/09687599.2018.1491390View
Published Version

Abstract

intellectual disability autism respite disability support worker family-centred person-centred UniSC Diversity Area - Disability and Inclusion UniSC Diversity Area - Life Stages
Parent-carers need support to continue to care for their child with significant disability in their home. There has, however, been little evidence that respite interventions have consistent or enduring beneficial effects on carer well-being. This article reports the findings of a qualitative study which adopted an Appreciative Inquiry philosophy to interview parent-carers of children with significant intellectual and/or developmental disabilities on how formal support services have helped them maintain their health and well-being, and disability support staff on how they help such parent-carers foster their health and well-being. We conclude that better communication and collaboration between service providers and users, more targeted training of workers, and embracing a person-centred and family-centred approach to respite services are needed. In addition, clearer definition and communication of the scope of respite services are required to best support families of children with significant disability in their home.

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Rehabilitation
Social Sciences, Interdisciplinary

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