You’re not alone. We recognize the importance of connection, education, and support for those living with dermatomyositis and related inflammatory myopathies. That’s why we proudly acknowledge the work of trusted organizations like:

The Myositis Association – a leader in patient advocacy, education, and research.

Myositis Support & Understanding (MSU) – a vibrant community offering peer support and resources for patients and caregivers.

Nori’s Fight – dedicated to raising awareness about the rare autoimmune disease dermatomyositis and promoting early detection and advancements in treatments for Anti-MDA5 Dermatomyositis and Interstitial Lung Disease.

These groups are part of the broader ecosystem of care and support. We encourage you to explore them further once you’re inside our subscriber community.