The 2026 Million Dollar Bike Ride takes place Saturday, June 13th. Check the MDBR site for more information and to sign up. ENDD director Ben Prosser will be riding with Lulu’s Crew, the team he and his spouse, Erin, created in honor of their own daughter, Lucy, who was born with STXBP1. You’re welcome to join them or choose a team fundraising for another rare disease.
Charlene Son Rigby, President and Co-founder of the STXBP1 Foundation, interviews ENDD’s Mike Boland about STXBP1 therapeutic development updates from the annual meeting of the American Society for Gene and Cell Therapy.
From The Transmitter, by Lydia Denworth.
A handful of scientists are committed to advancing research on the autism-related genetic conditions their own children have.
SynGAP Research Fund’s annual 5k 🏃🏾️ takes place this year on April 27, 2024. Families can set up teams at Syngap.Fund/Sprint24! This event helps increase awareness of SYNGAP1 in our communities by giving families an easy way to reach out to friends and family for support.