The Cute Syndrome Foundation

The Cute Syndrome Foundation raises awareness of SCN8A mutations, funds the dedicated and talented scientists researching SCN8A, and supports the families around the world who are affected by this disorder.

Celebrating 11 years of advocacy, awareness, support and inclusion

Created 2 years ago

Created 3 years ago

Created 4 months ago

Bring hope and joy to SCN8A Families through the Connor James Smith Patient Assistance Grant

Created 5 months ago

Celebrating 12 years of impact, dedication, and hope in the SCN8A community

Created 1 year ago

Help us reach our 2024 goals and support SCN8A families through 2025 and beyond.

Created 1 year ago

Created 1 year ago

This Giving Tuesday, your gift helps us bring joy to SCN8A patients and their families!

Created 1 year ago