In many countries social policy has seen a growing concern for citizen control and empowerment which has led to an increase in person centred approaches to social care, referred to a personalisation. The National Disability Insurance scheme (NDIS) is one of the most ambitious personalisation schemes in the world and aims to give choice and control over services and supports for people who acquire a permanent disability, thereby boosting citizen empowerment and improving social and health outcomes. However a new research paper by Gemma Carey, Eleanor Malbon, and Ariella Meltzer suggests that the ability to have choice and control in personalisation schemes can be distributed unequally. They use to context of the NDIS to examine how some Australians with disability may be missing out on accessing the care they are entitled to.
This piece originally appeared in The Conversation and was authored by Eleanor Malbon and Gemma Carey.
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