In celebration of International SCN2A Awareness Day on February 24th, we explore how SCN2A, a rare genetic disease, impacts each child. You’ll hear from four moms with four very different children. They will show us what life has looked like for them since their diagnosis and what they are doing as a result of knowing the genetic cause for their children’s medical conditions.
A BIG thank you to the four parents who shared their voices and stories for this episode.
- Katie Loosley
- Nikki Beasley
- Jenna Puteri
- Kris Ray
Other episodes from SCN2A parents
Seizing Joy and Grace with Tracy Umezu
Growing a Family Gratefully with Rachael Lividini
The Art of Supporting the Special Needs Mom
Links
FamilieSCN2A Global Support Group
SCN2A Related Autism & Epilepsy: The FamilieSCN2a Foundation
Simon Searchlight - SCN2A (Research)
Look to Learn - Activities for Eye Gaze
Children’s Hospital of Philadelphia - Dr. Ingo Helbig
Children’s Mercy - Dr. Coffman