About Us
The Tourette Syndrome Association of Australia (TSAA) is the primary national peak body and registered charity representing individuals, families, and professionals affected by Tourette syndrome and chronic tic disorders across Australia.
Founded in 1989 by a group of concerned parents and medical professionals it has grown into a professionally headed board run charity, but never lost it’s community-focused attitude, remaining dedicated to leading the way in research, breaking down isolation and driving advocacy nationwide.
In a world built for neurotypical minds, living with a neurodivergent condition in Australia can feel like an uphill battle against systemic misunderstandings, delayed diagnoses, and social isolation.
We exist to bridge that gap. By combining lived experience with evidence-based advocacy, we equip individuals, families, and communities with the tools to champion neurodiversity—not just tolerate it.
An estimated 50,000 Australians live with Tourette syndrome or chronic tic disorders, and over 90% navigate co-occurring neurodivergent traits like ADHD, Autism, or OCD.
Despite how common these conditions are, neurodivergent Australians face distinct challenges:
Diagnostic Roadblocks: Waiting over two years for an accurate diagnosis, often while struggling in school or work environments.
Systemic Gaps: Facing high rejection rates for disability support services (such as the NDIS) and a shortage of neuro-affirming care.
Social & Workplace Stigma: High rates of bullying in schools and discrimination in the workforce due to misunderstood tics or sensory differences.
Whether you're a parent seeking answers, an individual looking for community, or an ally ready to create a more inclusive Australia—there is a place for you here. Together, we are breaking down stigma, reforming policy, and building a world where every brain is valued.