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

NeedyMeds

TMA is hosting a webinar on October 29th at 1:00pm EST with guest speaker, Carla Dellaporta from NeedyMeds.

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2019 Annual Patient Conference

Nearly 500 people attended TMA’s 2019 Annual Patient Conference, learning about their disease and sharing experiences with others who also live with or care for someone with myositis.

Presentations are available by session.

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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.

See All of Our Stories

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!

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