Volume 30, Issue 2 pp. 208-217
ORIGINAL RESEARCH

Lived experience of parents and carers of people receiving services in rural areas under the National Disability Insurance Scheme

Alexandra Prowse BOccThy (Hons)

Alexandra Prowse BOccThy (Hons)

University of Newcastle, School of Health Sciences, Callaghan, NSW, Australia

Contribution: Formal analysis, ​Investigation, Writing - original draft

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Rebecca Wolfgang MPhil

Rebecca Wolfgang MPhil

University of Newcastle Department of Rural Health, Tamworth, NSW, Australia

Contribution: Conceptualization, ​Investigation, Project administration, Supervision, Writing - review & editing

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Alexandra Little BSPath(Hons)

Alexandra Little BSPath(Hons)

University of Newcastle Department of Rural Health, Tamworth, NSW, Australia

Contribution: Conceptualization, Supervision, Writing - review & editing

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Katrina Wakely BAppSc(OT)

Katrina Wakely BAppSc(OT)

University of Newcastle Department of Rural Health, Tamworth, NSW, Australia

Contribution: Conceptualization, Project administration, Supervision, Writing - review & editing

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Luke Wakely PhD

Corresponding Author

Luke Wakely PhD

University of Newcastle Department of Rural Health, Tamworth, NSW, Australia

Correspondence

Luke Wakely, Senior Lecturer in Physiotherapy & Academic Team Leader North West University of Newcastle Department of Rural Health, 114 – 148 Johnston Street Tamworth, Tamworth, NSW, Australia.

Email: [email protected]

Contribution: Conceptualization, Methodology, Project administration, Supervision, Writing - review & editing

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First published: 25 January 2022
Citations: 4

Abstract

Objective

The purpose of this study was to investigate the lived experience of parenting or caring for a person with a disability receiving services under the National Disability Insurance Scheme in rural Australia.

Design

Qualitative study guided by the phenomenology of practice.

Setting

Rural areas of New South Wales (MM 3-7).

Participants

Participants were 5 parents and one carer of people receiving National Disability Insurance Scheme services who resided in rural New South Wales.

Design

Participants engaged in a semi-structured interview about their lived experiences caring for someone accessing services under the National Disability Insurance Scheme in rural New South Wales. Interviews were audio-recorded, transcribed verbatim and analysed thematically.

Results

Three themes emerged from the data analysis. ‘More than a disability’ described the absence of understanding of family and carer challenges when National Disability Insurance Scheme plans were designed and implemented. ‘Fighting for funding and services’ described that while the National Disability Insurance Scheme increased funding support, parents and carers experienced limited support navigating the National Disability Insurance Scheme. ‘Cold as Ice’ encompassed parents' and carers' descriptions of their relationship with National Disability Insurance Scheme staff. These challenges were further impacted by the limited choice and availability of health service providers in rural areas.

Conclusion

Participants felt that the National Disability Insurance Scheme had created additional stress and confusion in their lives and at times had hindered the achievement of the goals of their family member with a disability. The voices of parents and carers is a critical one, and it is essential that rural parents' and carers' needs are considered and supported in future planning of the National Disability Insurance Scheme.

CONFLICT OF INTEREST

The authors declare no conflict of interest. No funding was received for this project.

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