Abstract: Disability reform in Australia centres on a National Disability Insurance Scheme (NDIS), which aims to provide lifelong, individualised support based on the principle of ‘reasonable and necessary’ care. As a universal rights‑based scheme it represents a historical shift in allocation principles in Australia’s disability policy. Nonetheless, attention will be on determining who receives what care given the diversity of personal and family contexts. The aim of this paper is to discuss the operational complexities of a principle of reasonable and necessary care with reference to the findings of a three‑year study on the experiences and perspectives of disability care of 25 adults with acquired disability, their 22 nominated family members and 18 service providers. Evidence from this study suggests enacting the principle of reasonable and necessary care and support will be problematic, in particular as it relates to personalising the level and scope of services, balancing formal and informal care, and principles of equity. The paper contributes to the literature about allocation principles in social policy and the challenges of implementation. Further, it provides an empirically informed discussion of some of the specific policy implementation challenges concerning the NDIS. Keywords: disability care, policy allocation principles, national disability insurance scheme, evidence‑based policy, qualitative research
Foster, Michele; Henman, Paul; Tilse, Cheryl; Fleming, Jennifer; Allen, Shelley; et al. Australian Journal of Social Issues; Sydney Vol. 51, Iss. 1, (2016): 27-46,109-110. http://search.proquest.com/openview/6c96ac58bfe7f6bee77bb6fe33ef293f/1?pq-origsite=gscholar&cbl=49075
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