👉 Register here TMA Georgia Myositis Support Group meets every fourth Saturday from 10:30–11:30 AM ET, except December. Peer-led support groups matter at every stage of the journey. Even if...
As we close out the year, we all have an opportunity to make a meaningful difference for individuals and families living with myositis. Your year-end gift to The Myositis Association...
Every day, individuals living with myositis face muscle weakness, fatigue, isolation, and uncertainty. But they don’t have to face it alone. Through education, support groups, research funding, and advocacy, The...
Register Here Join the TMA Minnesota & Wisconsin Myositis Support Group: Connect, Share, and Find Support This group offers a welcoming space for individuals living with myositis to connect, share experiences,...
Register Here Join TMA's Flying Solo Affinity Group: Support for Those Living with Myositis Without a Live-In Care Partner The TMA Flying Solo Affinity Group is a dedicated space for...
Register Here Join TMA’s Women of Color Affinity Group: Empowerment Through Support & Advocacy Founded in 2019 by Holly Jones and Kaniah Gunter, TMA’s Women of Color (WOC) Affinity Group...
Please note there will be no July meeting to allow our volunteers to celebrate the holiday with their families. Join the TMA Care Partner Affinity Group: A Space Just for...
TMA’s Worldwide Myositis Support by Diagnosis Group is open to all, especially those without an active support group in their local area. Formally known as Nationwide, this group has hosted international...
Γνωρίστε άλλους σαν εσάς, μάθετε, μοιραστείτε και συνδεθείτε! Συναντιόμαστε κάθε μήνα την πρώτη Δευτέρα. Εγγραφείτε εδώ
Join fellow members of the myositis community for the TMA Arkansas Support Group, a welcoming space to connect, share, and learn together. When: Second Tuesday of every month, 12:00-1:00 PM...
What role might the trillions of microbes in our gut play in myositis? Join The Myositis Association for the next webinar in our Myositis Research Insights series, featuring Dr. Lisa...
The HSS Myositis Support Group is open to people living with myositis, their families, and friends. If this is your first time attending the HSS group meeting, please be sure...