The use and experience of the national disability insurance scheme for Australians with skeletal dysplasia: a mixed-methods study

Despite all participants demonstrating a need for assistance to achieve functional independence, experience and success in accessing the NDIS were varied. Both positive and negative impacts were reported when accessing, or attempting to access the NDIS. To promote more equal and equitable NDIS access for individuals with skeletal dysplasias, NDIS and condition-specific knowledge is recommended for all stakeholders. Finally, further evaluation is needed to ensure future NDIS eligibility changes provide access to those who are potentially eligible but currently rejected.

Authors

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Publication Details

Journal
Orphanet Journal of Rare Diseases
Published
2025-03-05
DOI
https://doi.org/10.1186/s13023-025-03630-6
Citations
1
Primary Topic
Primary Care and Health Outcomes
Type
article
Field-Weighted Citation Impact
2.82
Controls
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article

The use and experience of the national disability insurance scheme for Australians with skeletal dysplasia: a mixed-methods study

Ashley Woodbury, Verity Pacey, Penelope J. Ireland, D. T. Nguyen et al.
1 citations
Orphanet Journal of Rare Diseases
Primary Care and Health Outcomes
2.82
article

The use and experience of the national disability insurance scheme for Australians with skeletal dysplasia: a mixed-methods study

Ashley Woodbury, Verity Pacey, Penelope J. Ireland, D. T. Nguyen, Joyce Ching‐Jung Lai
article en
1 citations

Abstract

Despite all participants demonstrating a need for assistance to achieve functional independence, experience and success in accessing the NDIS were varied. Both positive and negative impacts were reported when accessing, or attempting to access the NDIS. To promote more equal and equitable NDIS access for individuals with skeletal dysplasias, NDIS and condition-specific knowledge is recommended for all stakeholders. Finally, further evaluation is needed to ensure future NDIS eligibility changes provide access to those who are potentially eligible but currently rejected.

Orphanet Journal of Rare DiseasesVol. 20(1)
Children's Health Queensland Hospital and Health Service (AU), Macquarie University (AU)
Openalex Percentile: Top 13%
Primary Care and Health Outcomes
2.82
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