January 30, 2017
WASHINGTON – Families of over 150 children globally struggling with SCN8A - a rare but devastating genetic disorder - are joining forces to educate the public about SCN8A and the urgency for accelerating scientific progress.
The First International SCN8A Awareness Day i...
2019 - The Year in Review
December 31, 2019
Helping families find the critical information and support they need
December 11, 2019
2019 Wishes for Elliott - AES Grantee
July 10, 2019
Exploration of Synergies Across Sodium Channelopathies Yields New Collaboration and Research Strategies
November 11, 2018
July 23, 2018
Multi-Disciplinary SCN8A Epilepsy Clinic Updates
August 11, 2017
Wishes for Elliott Continues to Forge Breakthroughs in the Science of SCN8A
June 13, 2017
Small Family Foundation Partners with University of Michigan to Develop SCN8A Mouse Models of Most Severe Mutations
June 12, 2017
Help Protect All People with Rare Diseases
March 7, 2017
Report from Rare Disease Week in D.C.
March 2, 2017
Gabi and John on their decision to launch "Wishes for Elliott"
November 26, 2014
Events & Updates