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

FDA's Role in Drug Development & Rare Disease

Please Join on July 30th 11am - 12 noon EST for a very special webinar with FDA.

Learn More

2019 Annual Patient Conference

WHO YOU ARE MATTERS

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.

Learn More

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

See All Upcoming Events

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.

Stay Up-to-Date