Address book
Rare Voices Australia (RVA) is the national peak body for Australians living with a rare disease. Established in 2012, RVA works with all key stakeholders to drive the best outcomes for Australians living with a rare disease.
A tax-deductible registered charity, formed in 1988 to provide support and information for individuals and families affected by a genetic condition.
A patient-run non-profit organisation founded in 1994 that supports individuals with Fabry across Australia.
A non-profit association with the mission to Improve the health and wellbeing of Australian and New Zealander Gaucher patients through community building, education, advocacy, and support of research.
Transplant Australia is a national charity dedicated to supporting transplant recipients, living donors, donor families, and those awaiting transplants through advocacy, education, and programs that promote active lifestyles and raise awareness about organ and tissue donation.
A not-for-profit patient advocacy organisation dedicated to serving persons with hereditary angioedema, in Australia and New Zealand.
At Arrow, our target is clear. We aim to provide personalised support, healthcare training and research funding to help every Australian enduring tough but lifesaving bone marrow and stem cell transplants.