Caretaker's Corner - Wishes for Elliott

Report from Rare Disease Week in D.C.

March 2, 2017

It has been an amazing week to come together with rare disease advocates from 48 states representing over 160 rare disease to advocate for policies supportive of our communities. We are so strong together – over 30 million Americans are affected by a rare disease – 50%...

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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

June 12, 2017

Gabi and John on their decision to launch "Wishes for Elliott"

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

June 13, 2017

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Report from Rare Disease Week in D.C.

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