MyoCon! September 24–27, 2026.
By Julia Nickerson On June 1, I had the privilege of helping launch an exciting chapter of the Visiting Professor Program at the University of California, San Francisco (UCSF). As…
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Fantasy Football for TMA: Competition, Camaraderie, and Support for the Myositis Community
Looking for a fun way to connect with others while supporting The Myositis Association (TMA)? TMA’s Fantasy Football leagues offer the perfect combination of friendly competition, community engagement, and fundraising…
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Preventing DM Flares: There’s an App for That
By Darlene Butler Many dermatomyositis patients fight for months to get answers, and there is a sense of relief when you hear “you have dermatomyositis.” Then treatment brings a new…
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Finding Strength Through Advocacy
By Deidre M. Champion Before myositis became part of my life, I was always active. I used to run track and compete in hurdles, and I spent a lot of…
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A New Model for Understanding IBM
Each year, TMA awards research funding to support innovative investigations to improve understanding and treatment of myositis diseases. Dr. Thomas Lloyd recently completed such a project in which he and…
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