Dec 8, 2021, 2:32 PM
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Those living with a rare disorder in New Zealand experience inequitable, ineffective, and/or no access to the diagnostic and treatment services they require for them to have healthy futures. This is due to a combination of lack of clinician awareness and systemic barriers to appropriate services which are embedded within the current health system. We have the opportunity to improve this picture.

Read RDNZ's full submission to the Pae Ora Legislation Committee here:


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