Caretaker's Corner - Wishes for Elliott

A bright future -- The Joy of Learning

August 15, 2014

The roller coaster of emotions associated with the hundreds of visits with Elliott’s many doctors is indescribable. With so little known about Elliott’s underlying disease, tests and reports from doctors have so often been frustrating, confusing and without clear resul...

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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"

November 26, 2014

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

June 13, 2017

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A bright future -- The Joy of Learning

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