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

A Dad's Eye View 

The Art of Supporting the Special Needs Mom



FamilieSCN2A Foundation

FamilieSCN2A Global Support Group

SCN2A Related Autism & Epilepsy: The FamilieSCN2a Foundation

SCN2A Australia

SCN2A Insights Podcast

SCN2A Families UK - FB page

SCN2A Europe

Simon Searchlight - SCN2A (Research)

SPARK for Autism - SCN2A

A Walk with Jo Facebook Page

Eye Gaze - Think Smart Box

Look to Learn - Activities for Eye Gaze

Children’s Hospital of Philadelphia - Dr. Ingo Helbig

Children’s Mercy - Dr. Coffman


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