Providing Education, Research, and Support to the Myositis Community
What is Myositis?
Myositis is a muscle-wasting disease that results in fatigue and reduced strength.
Visit the Myositis Library
Browse our library to find helpful discussions, presentations and research studies.
See TMA in the News
Check out recent blog posts to stay up-to-date on TMA and myositis news.
Get Involved
We always welcome new members to our community. Join by volunteering, fundraising, and more.
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.
Learn More
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.
Learn MorePatient Stories
Each person's journey is unique, yet familiar. Listen to those living with myositis share their stories of persistence and hope.
John Mozer: Sporadic Inclusion-Body Myositis
Dale Scott: Polymyositis
Bill Simeral: Polymyositis
Michael Bradbury: Sporadic Inclusion-Body Myositis
Upcoming Events
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CA Northern Support Group Meeting Saturday, October 26, 2019 | 10:00 am – 3:00 pm
If you need directions, please click here: www.edenmedcenter.org Lunch is available at the cafeteria in the main hospital, or you may…
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Wisconsin KIT Support Group Meeting Saturday, October 26, 2019 | 11:30 am – 2:30 pm
Research shows that people who receive support from a social network cope better, feel more in control, and have better…
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FL Northeast KIT Support Group Meeting Saturday, November 2, 2019 | 11:00 am – 1:00 pm
Research shows that people who receive support from a social network cope better, feel more in control, and have better…
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!
