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…
Continue Reading
Announcing the Marianne Moyer Myositis Leader Award
The Myositis Association (TMA) is proud to announce the inaugural Marianne Moyer Myositis Leader Award to be presented at the 2024 Heroes in the Fight Awards Celebration on September 7…
Continue Reading
Last call for comments for DM PFDD
TMA was honored to partner with Myositis Support and Understanding (MSU) to host the Externally Led Patient Focused Drug Development (PFDD) meeting for adult dermatomyositis (DM) on June 7. View…
Continue Reading
Raising the voice of patients in research
TMA medical advisor and patient advocate Ingrid de Groot insists patients be involved in medical research.
Continue Reading
Wellness and self-care while living with myositis
Many community members responded when we asked them to share their stories and insights to help others. Here is some of the best wellness and self-care advice from fellow TMA members!
Continue Reading