The Cute Syndrome Foundation: SCN8A Epilepsy Support, Awareness, and Research
  • Home
  • About
    • About SCN8A
    • About Us
    • Volunteers
    • Sponsors
    • 2018 Annual Report
  • Families
    • SCN8A Warriors
    • Reference Guide
  • Events
    • Annual SCN8A Clinician, Researcher, and Family Gathering
    • Researcher Roundtable
    • Awareness Day
  • Research
    • Research Grants
    • SCN8A Registry
  • Donate
    • How You Can Help
    • PLAE
  • Contact
  • Blog
  • Shop

The Cute Syndrome in the News!

12/21/2018

0 Comments

 
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! ​​​
0 Comments



Leave a Reply.

    Author

    Write something about yourself. No need to be fancy, just an overview.

    Archives

    September 2019
    August 2019
    July 2019
    January 2019
    December 2018

    Categories

    All

    RSS Feed

Past Annual Reports

Past PCDH19 Efforts

​
The Cute Syndrome is registered as a tax-exempt organization under IRS section 501(c)(3).
​
​Our tax identification number is: 46-2699066.

© The Cute Syndrome Foundation, All rights reserved
  • Home
  • About
    • About SCN8A
    • About Us
    • Volunteers
    • Sponsors
    • 2018 Annual Report
  • Families
    • SCN8A Warriors
    • Reference Guide
  • Events
    • Annual SCN8A Clinician, Researcher, and Family Gathering
    • Researcher Roundtable
    • Awareness Day
  • Research
    • Research Grants
    • SCN8A Registry
  • Donate
    • How You Can Help
    • PLAE
  • Contact
  • Blog
  • Shop