Self directed disability support (SDDS): building community capacity through action research
Authors: Karen R Fisher, Sam Cooper, Christiane Purcal, Ngila Bevan and Ariella Meltzer
Published: 12th April 2013
Disability support has historically been organised and financially managed through government and service provider agencies (agency funding). Increasingly it is offered through individualised, person-centred packages of support (individual or self-directed funding), which allow people to manage how their own funds are spent. Opportunities for self-directed disability support (SDDS) – in both agency and individual funding approaches - are expanding across Australian states and territories, in line with the National Disability Insurance Scheme (NDIS) reforms.
This project explores how people with disability manage the transition towardsself directed disability support.
Australian evidence on this critical topic is thin. We know little about the impact of self directed options on people requiring support, informal carers and support providers (Prideaux et al 2009). Likewise, there is little systematic information about the effectiveness of existing disability support systems (Baxter et al 2010). Such information is gathered in this project, and it is important for assessing the impact of new approaches on equity of access, quality and availability of support, and community outcomes (Ungerson & Yeandle 2007).
The Social Policy Research Centre (SPRC), University of New South Wales (UNSW), in collaboration with People With Disability Australia (PWDA) and the Centre for Children and Young People (CCYP), Southern Cross University (SCU), is conducting the project.
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