Health service experiences to address mobility decline in ambulant adults ageing with cerebral palsy

Prue Elizabeth Morgan, Dina Pogrebnoy, Rachael McDonald

Research output: Contribution to journalArticleResearchpeer-review

4 Citations (Scopus)

Abstract

Background Adults ageing with a disability need lifelong access to health services to meet their changing needs. This study aimed to explore in depth the experience and impact of health service access to address mobility change in adults ageing with cerebral palsy (CP).Method Semistructured interviews were conducted. Qualitative analysis and identification of themes were undertaken on resultant transcripts.Results Six community-living adults (35-52 years) with CP, at levels II and III of the Gross Motor Function Classification System-Extended Revised (GMFCS-E R), participated. All described adult-onset mobility decline and had experienced recent falls. Emergent themes explored the accessibility, nature, and type of health service available, comparisons to paediatric experience, and themes related to frustration, perceived control, and self-advocacy.Conclusion Adults with CP report variability in the access to and matching of health service provided with self-perceptions of service type and need to address mobility decline. Adults with CP describe frustration regarding their experiences and may seek opportunities to increase self-advocacy regarding available health and support service
Original languageEnglish
Pages (from-to)282 - 289
Number of pages8
JournalJournal of Intellectual and Developmental Disability
Volume39
Issue number3
DOIs
Publication statusPublished - 2014

Cite this

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title = "Health service experiences to address mobility decline in ambulant adults ageing with cerebral palsy",
abstract = "Background Adults ageing with a disability need lifelong access to health services to meet their changing needs. This study aimed to explore in depth the experience and impact of health service access to address mobility change in adults ageing with cerebral palsy (CP).Method Semistructured interviews were conducted. Qualitative analysis and identification of themes were undertaken on resultant transcripts.Results Six community-living adults (35-52 years) with CP, at levels II and III of the Gross Motor Function Classification System-Extended Revised (GMFCS-E R), participated. All described adult-onset mobility decline and had experienced recent falls. Emergent themes explored the accessibility, nature, and type of health service available, comparisons to paediatric experience, and themes related to frustration, perceived control, and self-advocacy.Conclusion Adults with CP report variability in the access to and matching of health service provided with self-perceptions of service type and need to address mobility decline. Adults with CP describe frustration regarding their experiences and may seek opportunities to increase self-advocacy regarding available health and support service",
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Health service experiences to address mobility decline in ambulant adults ageing with cerebral palsy. / Morgan, Prue Elizabeth; Pogrebnoy, Dina; McDonald, Rachael.

In: Journal of Intellectual and Developmental Disability, Vol. 39, No. 3, 2014, p. 282 - 289.

Research output: Contribution to journalArticleResearchpeer-review

TY - JOUR

T1 - Health service experiences to address mobility decline in ambulant adults ageing with cerebral palsy

AU - Morgan, Prue Elizabeth

AU - Pogrebnoy, Dina

AU - McDonald, Rachael

PY - 2014

Y1 - 2014

N2 - Background Adults ageing with a disability need lifelong access to health services to meet their changing needs. This study aimed to explore in depth the experience and impact of health service access to address mobility change in adults ageing with cerebral palsy (CP).Method Semistructured interviews were conducted. Qualitative analysis and identification of themes were undertaken on resultant transcripts.Results Six community-living adults (35-52 years) with CP, at levels II and III of the Gross Motor Function Classification System-Extended Revised (GMFCS-E R), participated. All described adult-onset mobility decline and had experienced recent falls. Emergent themes explored the accessibility, nature, and type of health service available, comparisons to paediatric experience, and themes related to frustration, perceived control, and self-advocacy.Conclusion Adults with CP report variability in the access to and matching of health service provided with self-perceptions of service type and need to address mobility decline. Adults with CP describe frustration regarding their experiences and may seek opportunities to increase self-advocacy regarding available health and support service

AB - Background Adults ageing with a disability need lifelong access to health services to meet their changing needs. This study aimed to explore in depth the experience and impact of health service access to address mobility change in adults ageing with cerebral palsy (CP).Method Semistructured interviews were conducted. Qualitative analysis and identification of themes were undertaken on resultant transcripts.Results Six community-living adults (35-52 years) with CP, at levels II and III of the Gross Motor Function Classification System-Extended Revised (GMFCS-E R), participated. All described adult-onset mobility decline and had experienced recent falls. Emergent themes explored the accessibility, nature, and type of health service available, comparisons to paediatric experience, and themes related to frustration, perceived control, and self-advocacy.Conclusion Adults with CP report variability in the access to and matching of health service provided with self-perceptions of service type and need to address mobility decline. Adults with CP describe frustration regarding their experiences and may seek opportunities to increase self-advocacy regarding available health and support service

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