The Myositis Association (TMA) is thrilled to introduce Tri Bourne, professional beach volleyball player and Olympian who is living with dermatomyositis. Tri will be honored with TMA’s Heroes in the…
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Poor sleep may make mobility worse
Myositis patients who already have difficulty with movement may want to take a look at their sleep patterns. The Nurse’s Health Study, a cohort study of more than 70,000 women…
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Press release: MAM Resolution in US House of Representatives
COLUMBIA, MD, UNITED STATES, May 1, 2025 /EINPresswire.com/ — May is Myositis Awareness Month, a time dedicated to raising awareness about a rare autoimmune disease that affects muscles and skin….
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TMA member and medical advisors pivotal in patient reported outcomes research
TMA is excited to announce that The Journal of Rheumatology recently published a pivotal study titled “The Dermatomyositis Disease Symptom Questionnaire (DM-DSQ): A Measure to Assess the Patient Experience of…
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TMA Hosts Patient Stories on Rare Disease Day
Rare Disease Day Summit highlights myositis and the 7000 other rare diseases affecting one in ten Americans COLUMBIA, MD, UNITED STATES, February 27, 2025 /EINPresswire.com/ — The Myositis Association (TMA),…
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