The Cute Syndrome Foundation: SCN8A Epilepsy Support, Awareness, and Research
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The Cute Syndrome in the News!

12/21/2018

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We had a chance to speak with WNYT News Channel 13 reporter Benita Zahn about Esmé and The Cute Syndrome. They put together a lovely story about us! ​​​
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  • Home
  • About
    • About SCN8A
    • About Us
    • Volunteers
    • Sponsors
    • 2019 Annual Report
  • Families
    • Join our SCN8A Community
    • SCN8A Warriors
    • Reference Guide
    • Shareable Resources
    • Family Meetup Grant Application
    • Gathering Family Portal
  • Events
    • Annual SCN8A Clinician, Researcher, and Family Gathering
    • Researcher Roundtable
    • Awareness Day
  • Research
    • Research Grants
    • SCN8A Registry
  • Donate
    • How You Can Help
    • SCN8A Awareness Gifts
  • Contact
  • Blog
  • Shop