My Nonprofit Reviews

Leah and the entire FamilieSCN2A team are incredible patient advocates for the SCN2A community. Their passion, drive and relentlessness are infused into everything they do and their work will improve the lives of families living with this devastating disease.

I'm honored to be a member of the CACNA1A Foundation's Board of Directors because I believe deeply in the promise of the Foundation's mission to accelerate the development of treatment options for CACNA1A children, and I share the sense of urgency that drives the Foundation's work.