Scleroderma (also known as systemic sclerosis) is a rare, chronic autoimmune connective tissue disease. Its cause is unknown, there is no cure, and it can affect every part of daily life.
That’s why Scleroderma Australia exists – to bring people together, raise awareness, and drive real change for the six thousand Australians living with this condition.
Funds raised support our national work to:
Scleroderma Australia is governed by a national Committee with delegates from each State organisation, ensuring strong collaboration and lived‑experience leadership across the country.
You don’t need to run a marathon to make a difference (unless you want to!).
Here are just a few ideas to get you started:
Every fundraiser, big or small, helps drive awareness and change.
Not able to fundraise right now? You can still make a powerful difference.
A small regular donation (weekly or monthly) helps Scleroderma Australia:
Even a few dollars a month adds up to life‑changing impact.
To learn more about Scleroderma Australia, become a member, or get involved, contact us directly or reach out to your local State association.
State associations run support groups and are deeply committed to supporting people with scleroderma, their families, friends and carers.
Together, we can fund hope, research, and better futures.

Scleroderma Australia