Syngap Research Fund, 501(c)(3)

SYNGAP1 Stories

Join heartfelt conversations with families and experts impacted by SYNGAP1-related disorders. Discover stories of resilience, hope, and community support in every episode.

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Eric Moulton, SRF Board Member and SYNGAP1 Dad, talks about Phoebe, schools, receiving her diagnosis, raising $60,000+ for Sprint4Syngap, and more!

E33 • 41 mins • Apr 8, 2025

Recent Episodes

Apr 8, 2025

Eric Moulton, SRF Board Member and SYNGAP1 Dad, talks about Phoebe, schools, receiving her diagnosis, raising $60,000+ for Sprint4Syngap, and more!

E33 • 41 mins

Mar 18, 2025

Kathryn Helde, SRF's CSO and SYNGAP1 Mom talks about her adult son Joey, genetic testing, hippotherapy, and Joey's words!

E32 • 48 mins

Feb 18, 2025

Chelsey and Anthony Navarro, SRF's Science Writer and Resource Mobilization Director (resp.), talk about daughter Emmy, grieving, preparing for the future, and expanding your community.

E31 • 54 mins

Dec 31, 2024

Zoe Bailey, SRF's Volunteer Coordinator, talks about finding SRF, volunteering, the SYNGAP1 conference and Zoe's daughter Kaia.

E30 • 47 mins

Nov 19, 2024

Stacey Miller, 2024 SYNGAP1 Conference Director, chats with new co-host Rainy Schlosser about the conference and Stacey's son, Jack.

E29 • 36 mins

Language
English
Country
United States
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