When the NIH and FDA canceled their Rare Disease Day celebration in Bethesda on February 28, TMA brought the myositis community together virtually for the We Care for Rare Summit….
Continue Reading
When the NIH and FDA canceled their Rare Disease Day celebration in Bethesda on February 28, TMA brought the myositis community together virtually for the We Care for Rare Summit….
Continue ReadingOn Monday, February 10, 2025, Rich DeAugustinis, Vice Chair of TMA’s Board of Directors, testified to the Georgia Senate Committee on Health and Human Services in support of the Georgia Hope…
Continue ReadingThe Myositis Association (TMA) recognizes that the best hope for a cure for myositis diseases lies in research. Since 2002, TMA’s annual research grants program has approved 68 projects totaling nearly…
Continue ReadingAs 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 Reading