March 31, 2014
Every child we see seems better off than Elliott.
Frequent visits to the hospital often present children who may have profound challenges but each of whom seem to have some or many capabilities, all of which Elliott lacks: They see. They speak. They can sit. They talk....
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
A Countdown of Seven Actions to Support SCN8A Children and Families
February 20, 2017
Gabi and John on their decision to launch "Wishes for Elliott"
November 26, 2014
Events & Updates