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The Map-HD Registry, led by the Huntington’s Disease Network of Australia (HDNA), seeks to map HD across Australia. By registering yourself or your loved ones, you will be contributing towards a project that aims to:
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- Identify where improved clinical care and services are needed across Australia,
- Find those who are eligible for new services and treatments as they become available,
- Connect the members of the community to the research and clinical trial opportunities,
- Generate new knowledge about HD, and
- Inform the development of therapeutics.
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Want to know more? Click the button below to understand “Why Map-HD?“
Click below to register!!