About us

We’re a member-based organisation supporting people affected by Turner Syndrome across Australia. With branches in all States and territories, there’s lots of opportunities to get involved.

Position Statement

Empowering lives affected by Turner Syndrome through support, education, advocacy, and community.

The Turner Syndrome Association of Australia Limited (TSAA) is the national not-for-profit organisation dedicated to supporting individuals with Turner Syndrome, their families, carers, and health professionals. Founded and led by the community it serves, TSAA provides vital resources, creates inclusive connections, and promotes awareness and understanding of Turner Syndrome across Australia.

We believe that every individual with Turner Syndrome deserves the opportunity to thrive—physically, emotionally, socially, and intellectually. Through advocacy, education, and community engagement, we aim to remove barriers, reduce stigma, and improve lifelong outcomes.

Our Commitment:

• Support – Offering compassionate support to individuals with Turner Syndrome and their families across all stages of life.
• Education – Providing reliable, evidence-based information for the TS community, medical professionals, educators, and the public.
• Advocacy – Representing the voice of the TS community to government, health sectors, and the broader public to promote equitable access to care and services.
• Connection – Building strong networks through events, peer support, and online communities that reduce isolation and foster belonging.

As a trusted national voice, TSAA works in partnership with clinicians, researchers, educators, and families to improve health outcomes, raise awareness, and support lifelong well-being.