Caretaker's Corner - Wishes for Elliott

Rare Genetic Epilepsy Spurs Families into Action

January 30, 2017

PRESS RELEASE

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...

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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

New Hope!

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

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Small Family Foundation Partners with University of Michigan to Develop SCN8A Mouse Models of Most Severe Mutations

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Wishes for Elliott Continues to Forge Breakthroughs in the Science of SCN8A

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Rare Genetic Epilepsy Spurs Families into Action

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