TMA is pleased to announce they have awarded three new myositis research grants.
8-Oct-2018 5:00 PM EDT Add to Favorites
TMA hosts its Annual Patient Conference at the Louisville Marriott Downtown on September 6-9. With more than 500 myositis patients and family members in attendance, this conference promises to be the largest in TMA history.
28-Aug-2018 1:05 PM EDT Add to Favorites
The Myositis Association is pleased to announce the appointment of Mary McGowan as Executive Director.
7-Aug-2018 2:05 PM EDT Add to Favorites
The Myositis Association announces the launch of its newly redesigned website, making it easier for visitors to access evidence-based information about all forms of the rare autoimmune muscle disease known as “myositis.”
6-Jun-2018 2:05 PM EDT Add to Favorites
Myositis Awareness Month brings attention to a rare autoimmune disease of the muscle that can cause disability for children and adults.
1-May-2018 8:05 AM EDT Add to Favorites
The ability to diagnose myositis diseases and treat them properly just improved immensely with the publication of new, evidence-based classification criteria.
19-Dec-2017 1:10 PM EST Add to Favorites
The Myositis Association (TMA) hosts their 2017 Annual Patient Conference September 7-10 at the Sheraton San Diego Hotel and Marina. With more than 80 presentations and nearly 500 myositis patients, friends, and family members in attendance, this...
28-Aug-2017 9:05 AM EDT Add to Favorites
Dan Seftick thought his biggest challenge in life was his rare disease, dermatomyositis. When his son Greg tragically died in an avalanche while hiking in Grand Tetons National Park, he discovered there can be much bigger mountains to climb.
21-Aug-2017 9:55 AM EDT Add to Favorites
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May Is #MyositisAwareness Month. The Myositis Association Has Medical Experts Available to Speak About This Rare Autoimmune Disease of the Muscles. TMA@myositis.org
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27-Feb-2017 10:45 AM ESTsee all experts