Unsure whether to get the COVID-19 Vaccine?
Hear from fellow SCN8A parent and ER Doctor Luca

Our Recent Submission to the Food & Drug Administration in Support of SCN8A Treatments


The Faces of SCN8A

See how our early investigator grantees, in conjunction with the American Epilepsy Society, have helped advance the understanding of SCN8A and other rare epilepsies.

Partnerships for Progress

Wishes for Elliott has always understood the value of and sought out collaboration. We have an extensive list of groups we work closely with to make a difference in the lives of those with SCN8A and other rare epilepsies. A few of these key partnerships include our work with the American Epilepsy Society, National Institutes of Health, the Epilepsy Leadership Council, the Rare Epilepsy Network, a wide range of other rare epilepsy groups, University researchers, clinicians and beyond. 
Read more here


Wishes for Elliott is a family-based, non-profit organization dedicated to supporting research to improve the lives and prognosis of children struggling with SCN8A mutations and similar rare epilepsies.


Gabi, President and Co-Founder of Wishes for Elliott, was elected Co-Chair of the Epilepsy Leadership Council for a two year term, in 2020!

Resources for

SCN8A Families



- Q&A

- Where to Get Help

- Resources

Hear why Gabi
and John decided
to launch
Wishes for Elliott


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