Connect someone in your community with free, one-to-one information, support and navigation from a genetic counsellor. You can share the service, help someone make contact, or contact the Navigator on their behalf with their consent.
Refer to the Genetic Health Navigator →
Talk to us about an information or education session for your community on genetics, genetic services or another area where GAA may be able to help.
Confidential peer supervision for people supporting communities affected by grief, loss and complex experiences. A space to reflect on situations arising through your work and talk them through with an experienced grief counsellor.
Work with GAA and other rare disease organisations on issues and priorities that affect communities across conditions.
Explore collaborative advocacy →
Join focused groups bringing together people and organisations with a shared interest in particular issues affecting rare disease communities.
Our Annual Forum brings rare disease communities together with health professionals, researchers, policymakers and others across the sector. There are opportunities for rare condition organisations and groups to take part, share their work and connect with others.
Explore the GAA Annual Forum →
GAA works with community organisations on collaborative Rare Disease Day activities and events.
Get in touch with GAA to talk about what you are looking for and whether there is a way we can help.
Genetic Alliance Australia provides general information and support. Our information and Genetic Health Navigator service do not replace medical advice. We do not diagnose conditions, provide medical advice, recommend or interpret genetic testing or results, or make decisions about your healthcare. Please speak with an appropriate healthcare professional about your individual circumstances.
