Do you know about the Australian Haemochromatosis Registry?
To help with early diagnosis and treatment of haemochromatosis, the Australian Government is supporting Haemochromatosis Australia.
The Australian Government is providing $400,000 to create a new, nationwide, cloud-based patient registry.
Why it matters
The registry will collect health data from patients across the country. This data will help:
How you can help
The registry was launched on 14 August 2024 and is open for registration. If you have a patient with haemochromatosis, let them know about the register and encourage them to join it: https://registry.haemochromatosis.org.au/
For more information about haemochromatosis, visit www.ha.org.au or call 1300 019 028. Be part of this project and help improve the future of haemochromatosis treatment and research!
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