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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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Celebrate Rare Disease Day all month with rare disease events from TMA, FDA, and NIH! Rare Disease Day is a global initiative to raise awareness and generate support for everyone...
TMA and SAM are partnering for Autoimmune Awareness Month to have a conversation about living with myositis and long-term steroid use. This webinar will explore the physical, emotional, and practical...
Celebrate Rare Disease Day all month with rare disease events from TMA, FDA, and NIH! Rare Disease Day is a global initiative to raise awareness and generate support for everyone...
Join us for an informative and supportive Ask the Expert webinar featuring Dr. Suur Biliciler, a specialist in neuromuscular disorders and myositis care. This session will explore key aspects of...
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!
