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.
MAA Rare Voices Ambassador Lachy Beckett and MAA Secretary Anita Chalmers are interviewed by WIN TV. /www.facebook.com/watch/?v=464773856006052
Information about sun protection for children with juvenile dermatomyositis.
Robyn & Gordon discuss with the people from the Drive-able Podcast, their journey with obtaining a Wheelchair Modified Vehicle. Drive-able Podcast has a number of interesting videos here
A short guide to assist you in renewing your yearly membership. Should you need to update your password, click here for instructions. Please let us know if you encounter any issues with the payment or receipt facilities wherever you’re located. We will work quickly to rectify any issues. Should you need any assistance with your…