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.
REGISTER HERE FOR ZOOM TO ATTEND IN PERSON, EMAIL: SWFLKIT@YAHOO.COM Our fourth quarter meeting is Saturday, November 1, 2025 starting at 11 a.m. and ending around 3:15. All members, their...
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...
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!
What does a virtual pass provide? Five live, virtual sessions start August 21, and recorded sessions of breakouts (thirty-plus) will be available around October 15. 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!
