Blog - Page 13 of 34 - The Myositis Association

TMA’s top 10 travel tips

June 24, 2024June 24, 2024

TMA’s top 10 travel tips help you achieve those bucket-list wishes, including making the most of our International Annual Patient Conference.

Dermatomyositis: A many-headed monster

June 14, 2024June 14, 2024

The first-ever Externally Led Patient Focused Drug Development (EL-PFDD) meeting on June 7 offered a critical way for patients and their family members to highlight what life with DM is like.

Raising the voice of patients in research

June 13, 2024June 13, 2024

TMA medical advisor and patient advocate Ingrid de Groot insists patients be involved in medical research.

Robert Grun

May 31, 2024June 3, 2024

Robert Grun and his wife were expecting twins. Robert was in his mid-20s working as a compliance officer on mergers, acquisitions, and insider trading in a Wall Street firm in…

Wellness and self-care while living with myositis

May 30, 2024May 30, 2024

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!