Find a Support Group

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 KIT support group network.

Find a Support Group

2019 Annual Patient Conference

September 5-8, 2019
Minneapolis, MN

At TMA’s 2019 Annual Patient Conference in Minneapolis, Minnesota, the focus will be on addressing this diversity of needs and challenges within the myositis community.

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Position Your Myositis Grant for Success

Dr. Conrad "Chris" Weihl
Tuesday, April 9 at 12 noon ET

In this webinar, TMA medical advisor and research committee chair Dr. Conrad “Chris” Weihl speaks to investigators who hope to submit a research grant application as well as institutional leaders who advise trainees and early career faculty.

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Patient Stories

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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Upcoming Events

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TMA Grants and Fellowships

Research into myositis is a priority of TMA. TMA is actively engaged with the myositis research community in the U.S. and overseas. Through research, the mystery of myositis will be solved and, ultimately, a cure will be available.

Doctor conducting a medical interview

Community Forum

TMA offers its online Community Forum, which has multiple forums where you can post to reach other TMA members who have similar concerns as you.

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