In recognition of World Myositis Day (September 21), we are highlighting the stories of some of our overseas members. Your financial support enables TMA to help people in other countries who…
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Celebrating World Myositis Day: Myositis Africa
My name is Cynthia Ikediashi. I reside in Lagos, Nigeria. Early in 2009, while in my third year at the university, I started experiencing weakness in my arms, thighs, and…
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Celebrating our Myositis Connection: Reflections on TMA’s 2024 International Annual Patient Conference
By 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…
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TMA’s Women of Color raise the bar for advocacy and support
Kaniah Gunter and Holly Jones
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Karen Alexander: TMA’s 2024 Patient Ambassador Awardee
The 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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