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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2019 - The Year in Review

December 31, 2019

Helping families find the critical information and support they need

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2019 Wishes for Elliott - AES Grantee

July 10, 2019

Exploration of Synergies Across Sodium Channelopathies Yields New Collaboration and Research Strategies

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New Hope!

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Multi-Disciplinary SCN8A Epilepsy Clinic Updates

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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

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Rare Genetic Epilepsy Spurs Families into Action

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