The Cute Syndrome Foundation: SCN8A Epilepsy Support, Awareness, and Research
  • Home
  • About
    • About SCN8A
    • About Us
    • Partner Organizations
    • Volunteers
    • Sponsors
    • 2021 Annual Report
  • Families
    • Caregiver Support
    • Join our SCN8A Community
    • SCN8A Warriors
    • Educational Videos
    • Reference Guide
    • Resources
    • Shareable Graphics
  • Events
    • Annual SCN8A Clinician, Researcher, and Family Gathering
    • Researcher Roundtable
    • Awareness Day
  • Research
    • Clinical Trials
    • Research Grants
    • SCN8A Registry
  • Donate
  • Contact
  • Blog
  • Shop

TCSF Founder Hillary Savoie on Motherlode, the New York Times parenting blog

12/22/2018

0 Comments

 
Hillary Savoie's writing was featured on Motherlode, the New York Time parenting blog. In her post on June 28th she reveals some wonderful news about her daughter Esmé: Esmé can read. Check out the post here: http://parenting.blogs.nytimes.com/2015/06/28/esme-can-read

Hillary's writing also has recently appeared on The Mighty and Complex Child Magazine.
0 Comments



Leave a Reply.

    Archives

    January 2023
    July 2022
    March 2021
    December 2020
    November 2020
    September 2020
    January 2020
    December 2019
    September 2019
    August 2019
    July 2019
    January 2019
    December 2018

    Categories

    All
    Announcement
    Annual Gathering
    Awareness Day
    Community
    Drug Development
    Research

    RSS Feed

Past Annual Reports

Past PCDH19 Efforts

​Privacy Policy

The Cute Syndrome Foundation

PO Box 842 Ozark, MO 65721​
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
Picture
Picture
Picture
  • Home
  • About
    • About SCN8A
    • About Us
    • Partner Organizations
    • Volunteers
    • Sponsors
    • 2021 Annual Report
  • Families
    • Caregiver Support
    • Join our SCN8A Community
    • SCN8A Warriors
    • Educational Videos
    • Reference Guide
    • Resources
    • Shareable Graphics
  • Events
    • Annual SCN8A Clinician, Researcher, and Family Gathering
    • Researcher Roundtable
    • Awareness Day
  • Research
    • Clinical Trials
    • Research Grants
    • SCN8A Registry
  • Donate
  • Contact
  • Blog
  • Shop