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CureSYNGAP1
  • About SYNGAP1

    • What Is SYNGAP1?
    • SYNGAP1 Census
    • SYNGAP1 Treatment
    • SYNGAP1 Pipeline
    • SYNGAP1 & Epilepsy
    • Life Expectancy
    • SYNGAP1 & Autism
  • About CURE SYNGAP1

    • Mission & Values
    • CURE SYNGAP1 Impact
    • CURE SYNGAP1 Team
    • CURE SYNGAP1 Collective
    • Finances
    • Documents
    • Partners
    • Donors
    • Sponsors
    • Style Guide
    • Diversity, Equity, & Inclusion
  • Professionals

      Research

    • Request NHS Data
    • Grants

    • Current Grants
    • How To Apply
    • Press Releases
    • Models

    • iPS Cell Models
    • SYNGAP1 Mouse Models
    • Advisory Boards

    • Scientific Advisory Board
    • Clinical Advisory Board
  • Families

      Connections

    • Connect With CURE SYNGAP1
    • Join SYNGAP1 Registries
    • Join ProMMiS
    • Studies
    • Clinical Trials
    • Volunteer with CURE SYNGAP1
    • Fundraising
    • Medical

    • Resources for Undiagnosed
    • Doctors
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SYNGAP1 Stories

SYNGAP1 Stories

Stories shared by families about their lives raising Syngapians, co-hosted by Rainy Schlosser and Jo Ashline.

Listen below or find us on your podcast player of choice!

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AndĀ PLEASE – give us 5-stars everywhere – it matters!
SeeĀ cureSYNGAP1.org/RatingĀ to find out why!

Mike Graglia, May 2026 Update

Beata Tarasiuk – Part 2

Beata Tarasiuk – Part 1

Virginie McNamar

Kari Imperatore

John Hill

Nicole Ciccone

Jo Ashline

Eric Moulton

Kathryn Helde

Chelsey and Anthony Navarro

Zoe Bailey

Stacey Miller

Rainy Schlosser

Jackie Kancir

Paulina Polanco

Jessica Johnson

Hilary Volz

Guests’ Best Advice

The Best Of Ashley

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