Join us for a live Ask the Expert webinar focused on speech and swallowing difficulties (dysphagia) in myositis, featuring Dr. Georgia Malandraki, a member of The Myositis Association's Medical Advisory Board and an expert in swallowing disorders. Dysphagia is one of the most challenging and under-discussed symptoms of myositis, affecting communication, nutrition, and quality of...
Registration details coming soon! In partnership with the Thomas family, TMA is honored to offer the Meredith C. Thomas Memorial Fellowship, funding grants for early-career researchers and clinicians focused on learning more about how best to treat antisynthetase syndrome and interstitial lung disease. Meredith Thomas was diagnosed with antisynthetase syndrome and interstitial lung disease and...
Every day, individuals living with myositis face muscle weakness, fatigue, isolation, and uncertainty. But they don’t have to face it alone. Through education, support groups, research funding, and advocacy, The Myositis Association (TMA) connects patients and families to the resources and community they need to move forward with strength and hope. Your gift fuels critical...
May is Myositis Awareness Month! It’s a time for the myositis community to raise our collective voices and let the world know what this rare disease is all about. It’s TMA’s mission to support those who live with myositis and their care partners by bringing awareness, sharing resources and education, sharing strategies for advocacy, and building...
May is Myositis Awareness Month! It’s a time for the myositis community to raise our collective voices and let the world know what this rare disease is all about. It’s TMA’s mission to support those who live with myositis and their care partners by bringing awareness, sharing resources and education, sharing strategies for advocacy, and building...
May is Myositis Awareness Month! It’s a time for the myositis community to raise our collective voices and let the world know what this rare disease is all about. It’s TMA’s mission to support those who live with myositis and their care partners by bringing awareness, sharing resources and education, sharing strategies for advocacy, and building...
May is Myositis Awareness Month! It’s a time for the myositis community to raise our collective voices and let the world know what this rare disease is all about. It’s TMA’s mission to support those who live with myositis and their care partners by bringing awareness, sharing resources and education, sharing strategies for advocacy, and building...