The Cute Syndrome Foundation: SCN8A Epilepsy Support, Awareness, and Research
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    • About SCN8A
    • About Us
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    • Reference Guide
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    • CRF Gathering
    • Awareness Day
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Contact Us

If you are interested in volunteering, organizing fundraisers, or sponsorship opportunities contact Hillary Savoie.
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Contact Our Support Group

If your child has an SCN8A mutation, and you would like to join our Family Support Group on Facebook, send an email to scn8afamilies@gmail.com.
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  • Home
  • About
    • About SCN8A
    • About Us
    • Volunteers
    • Sponsors
    • 2017 Annual Report
  • Families
    • SCN8A Warriors
    • Reference Guide
  • Events
    • CRF Gathering
    • Awareness Day
  • Research
    • Research Grants
    • SCN8A Registry
  • Donate
    • How You Can Help
    • PLAE
  • Contact
  • Blog
  • Shop