Posted on May 27th, 2019
In 1979 Dr Alf Barnett introduced three of his Scleroderma patients to each other. They went on to form Scleroderma Victoria. We would like to mark our achievement of 40 years of providing support for people with Scleroderma, along with their family and friends, increasing community awareness of Scleroderma and supporting research into this chronic
Posted on December 13th, 2018
The most important thing to know is how do you meet the criteria to be eligible for the NDIS. From the perspective of Scleroderma, it is about thinking of the definition of disability. Your GP or Specialist needs to demonstrate the ‘how’ instead of the ‘what’ and determine the impact on your daily activities. For
Posted on November 15th, 2018
Hear honest accounts from Victorian patients who have been diagnosed with Scleroderma. For more information see our YouTube channel.
Posted on September 4th, 2018
Our Autumn Newsletter is now available to view. If you would like to see our current newsletter, become a member now.
Posted on July 1st, 2018
Thank you to the Grand Hotel Richmond for hosting our inaugural World Scleroderma Day lunch on June 30, 2018. Dyson Heppell, our Ambassador came along to do a quick Q&A on his great work in raising awareness and funds to support Mr H and Scleroderma. A Silent Auction with some great items from Dyson and
Posted on June 1st, 2018
Friday 29th June 2018 is World Scleroderma Day. And on this day Dyson Heppell, Captain of Essendon F C, will shave off his beard. Dyson Heppell and his little mate Harrison, or “Mr H” as he is often called are running a campaign throughout June called “Get behind the beard” to raise much needed funds
Posted on May 31st, 2018
Help us celebrate World Scleroderma Awareness Month and collect your spare change throughout the month of June. It’s easy – whether its a tin or a jar, its up to you. Slap on a sticker, and collect all the spare change you can. At the end of the month, put the change into the bank!