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 Support Group network.

Find a Support Group

Autoimmune Diseases and Nutrition

Wednesday, January 29, 2020 at 3pm ET.

Join Renee Lantner, dermatomyositis patient and former TMA Board member, and Susan Whitacre, MS, RD, LD, Dept of Neurology, University of Kansas Medical Center for a lively discussion on autoimmune disease and nutrition

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The Myositis Association's Corporate Video

Help us to advocate and motivate for change. Watch and share this new exciting video from The Myositis Association.

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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.

2019 Rare Champion of Hope: Collaboration In Research Award by Global Genes Nominated by The Myositis Association

More than 100 individuals and organizations worldwide were nominated by their peers for the 2019 RARE Champion of Hope Awards to honor their notable efforts in rare disease advocacy, science, medical care and treatment, and collaborations. Congratulations to IMACS for this prestigious award!

Who You Are Matters

2019 Annual Patient Conference

Our 2019 Annual Patient Conference brought myositis experts, researchers, doctors, patients, and care partners together to cover a variety of myositis topics in detail, explain new findings, and share personal experiences.

Myo-Thankful Journey

We are calling for those in the myositis community to reflect and share what you are most thankful for in your myositis journey.

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