As the TMA blog reflects, 2024 was a busy and exciting year for TMA! We published 45 posts, including 15 personal stories from members sharing how they live their best…
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TMA’s Global Myositis Patient Conference – Registration Rates Increase July 1!Register Now!
As the TMA blog reflects, 2024 was a busy and exciting year for TMA! We published 45 posts, including 15 personal stories from members sharing how they live their best…
Continue ReadingTMA deeply values every voice in the myositis community. Every day, we are inspired by individuals living and thriving with myositis. Through your generosity, we’ve been able to share powerful…
Continue ReadingBy Stanford Erickson Two women were, for me, like celebratory bookends to The Myositis Association’s International Annual Patient Conference in Baltimore September 6-8, 2024. One was the opening Friday night…
Continue ReadingKaniah Gunter and Holly Jones
Continue ReadingThe Myositis Association (TMA) is thrilled to recognize Karen Alexander, a groundbreaking Black supermodel who was diagnosed with dermatomyositis in 2016. Karen will be honored with TMA’s Heroes in the…
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