Supporting Rare Disease Advocacy at the 2023 World Muscle Society Conference

We would like to give a special thank you to the World Muscle Society for organizing an amazing conference in Charleston SC. We enjoyed catching up with our colleagues from rare disease advocacy groups, learning about the latest scientific advances from expert scientists and healthcare professionals on many aspects of neuromuscular diseases and visiting Charleston. We look forward to next year’s meeting in Prague!

On behalf of the Jain Foundation, Laura Rufibach, Co-President (right), and Kanan Lathia, Associate Director of Research (left) attended WMS 2023 in October.

The Jain Foundation team hosted an info table at WMS 2023.

Subscribe to Our Blog