• SCN2A Mutation Loss of Function, Global Delay

Hi, I'm Elizabeth.

Loves Mickey. Loves looking at herself in the mirror. Sings head, shoulders, knees and toes like it’s her job. Has the cutest run and cutest kisses.

Our Daughter, Elizabeth was diagnosed with SCN2A mutation loss of function in 2022. She’s now 2 years old. She has global delay. She does well with all of her therapies and is enrolled in school for fall 2023. Just learning about it all as a family.


Our goal is to find a cure!

Did you or your child just receive a new diagnosis of SCN2A? If so, please know you are not alone!