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If you are a member of TMA and are looking to talk with others about your disease to gain a better understanding and prepare for the challenges ahead, you are encouraged to join the Support Group network.
Find a Support GroupMyositis is a muscle-wasting disease that results in fatigue and reduced strength.
Browse our library to find helpful discussions, presentations and research studies.
Check out recent blog posts to stay up-to-date on TMA and myositis news.
We always welcome new members to our community. Join by volunteering, fundraising, and more.
Each person's journey is unique, yet familiar. Listen to those living with myositis share their stories of persistence and hope.
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TMA and SAM are joining forces for Autoimmune Awareness Month — and we're closing it out with a conversation you won't want to miss! Together, we're bringing the myositis and...
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...
Register Here Join The Myositis Association and the University of Kansas Medical Center for a free virtual regional conference designed for individuals living with myositis—including inclusion body myositis, immune-mediated necrotizing...
TMA Tennessee meets on the second Sunday of each month at 3:00 PM CT | 4:00 PM ET. Email leader Sharon Hinton at Hinton@myositis.org. Register here.
View one or all of the 40 presentations and info sessions about TMA’s conferences. Did you know TMA has been convening the only worldwide myositis patient conference annually since 1995? It is truly a “bucket list” experience!
Travel is difficult for many, and we want to share the MyoCon learnings as widely and inclusively as possible. That’s why we offer a package of recordings from most sessions on the conference agenda. A tremendous value for only $149 – purchase today!
Our increased virtual environment has allowed for connectivity that surpasses geographic location. In addition to our traditional KIT support groups, TMA is supporting meeting circles with outreach efforts targeted toward supporting and extending our organization’s reach into new communities.
May is Myositis Awareness Month! Celebrate with us by raising your voice and letting the world know what this rare disease is all about. It’s TMA’s mission to support those who live with myositis and their care partners by bringing awareness, sharing resources, educating patients and the public about myositis diseases, sharing strategies for advocacy, and building a stronger and more connected myositis community. Join us!
