Myositis Australia with Christine
A short video prepared for the May 2021 Myositis Summit hosted by The Myositis Association (USA) to introduce our Australian patient support group as a member of the World Myositis Coalition.

A short video prepared for the May 2021 Myositis Summit hosted by The Myositis Association (USA) to introduce our Australian patient support group as a member of the World Myositis Coalition.


MAA Rare Voices Ambassador Lachy Beckett and MAA Secretary Anita Chalmers are interviewed by WIN TV.

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Paintings by Jo Morris (dec 2022) and music by Lachy Beckett. Both Jo and Lachy survived JDM having developed it as very young children. Sadly Jo died at age 31. She was a fearless and much loved advocate who worked hard to build awareness for Myositis.

Ilana Strous discusses the role of a Speech Pathologist and the supports available to Myositis members experiencing difficulty with Speech and/or Swallowing.

Information about sun protection for children with juvenile dermatomyositis.