Literature DB >> 20850268

Health status and coping strategies among older parent-carers of adults with intellectual disabilities in an Australian sample.

Gwynnyth Llewellyn1, David McConnell, Lindsay Gething, Rosemary Cant, Hal Kendig.   

Abstract

BACKGROUND: Older parent-carers in Australia are the subject of increasing policy and practice attention due to concerns about their ongoing ability to care in the light of their own ageing and the ageing of their adult son or daughter. This paper examines health status and the coping strategies of a group of older Australian parents caring for an adult son or daughter with intellectual disabilities.
METHOD: Health status using the SF-12 (Ware, Snow, Kosinski, & Gandek, 1993), caring stress using the CADI (Nolan, Grant, & Keady, 1998), and coping strategies using the CAMI (Nolan et al., 1998) were assessed in 64 older parent-carers of adults with intellectual disabilities.
RESULTS: The self-reported health status of this sample of older parent-carers did not differ significantly from Australian population norms, with one exception. That is, the younger parent-carers in the sample (55-64 years) reported significantly poorer mental health. Better health was associated with having a partner, a larger and close support network of family, friends and neighbours, and a lower care-load. Overall, the study participants identified both satisfaction as well as stress associated with caring, a finding that runs counter to the common perception that being a carer is overwhelmingly burdensome. Common sources of stress were feeling helpless or not in control, and poor professional support. Analysis of older parent-carers coping strategies suggests that self-reliance, whether by choice or necessity, was the norm.
CONCLUSIONS: The health status of older parent-carers may present less cause for concern than anecdotal reports suggest. That said, the strong self-reliance particularly of the older carers presents a challenge to service providers seeking to engage those whose situation appears to warrant support from the service system.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20850268     DOI: 10.1016/j.ridd.2010.08.003

Source DB:  PubMed          Journal:  Res Dev Disabil        ISSN: 0891-4222


  4 in total

1.  Experiences and needs of carers of Aboriginal children with a disability: a qualitative study.

Authors:  Michelle DiGiacomo; Anna Green; Patricia Delaney; John Delaney; Patrick Patradoon-Ho; Patricia Mary Davidson; Penelope Abbott
Journal:  BMC Fam Pract       Date:  2017-11-29       Impact factor: 2.497

2.  Coping strategies of families of persons with learning disability in Imo state of Nigeria.

Authors:  Ngozi E Chukwu; Uzoma O Okoye; Nkechi G Onyeneho; Joseph C Okeibunor
Journal:  J Health Popul Nutr       Date:  2019-03-27       Impact factor: 2.000

3.  Mental health and well-being of fathers of children with intellectual disabilities: systematic review and meta-analysis.

Authors:  Kirsty Dunn; Deborah Kinnear; Andrew Jahoda; Alex McConnachie
Journal:  BJPsych Open       Date:  2019-11-07

4.  Parental Stress and Family Quality of Life: Surveying Family Members of Persons with Intellectual Disabilities.

Authors:  Cristina Jenaro; Noelia Flores; Belén Gutiérrez-Bermejo; Vanessa Vega; Carmen Pérez; Maribel Cruz
Journal:  Int J Environ Res Public Health       Date:  2020-12-03       Impact factor: 3.390

  4 in total

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