Milo, 21 months, died of infantile GM1 gangliosidosis on July 20, 2026. GM1 took his movement & sight, but he smiled & knew his parents' voices. His mom shared his story so we remember the joy he brought. Read it at curegm1.org/milos-story (link in bio). #GM1 #RareDisease

October's The Catalyst is live! 🎃💜 We're energized by last month's accomplishments and our annual conference. Get a preview, then read the full newsletter at https://www.curegm1.org/october-2026-cure-gm1-catalyst/ #CureGM1 #GM1Gangliosidosis #GM1

GM1 Community Conference is live! 💙 Huge thanks to our 2026 speakers for sharing their knowledge and dedication, and to our sponsors for their vital support of this conference and the GM1 community. #GM1 #GM1Gangliosidosis #CureGM1

Hope is possible. Enzyme replacement therapy could help people of all ages impacted by GM1. Learn more and support the project at curegm1.org/ert-project #GM1 #CureGM1 #ERT

GM1 gangliosidosis is most often inherited when both parents carry one changed gene. Learn more at curegm1.org/about-gm1 #GM1 #GM1Gangliosidosis #RareDisease