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
WHAT
IS
SCN8A EPILEPSY?
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.
EXCITING NEWS!
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!
PROGRESS? Review the incredible progress we have made since starting in 2014!
PARTNERSHIPS? Wonder how we are able to have so much impact when we are so small?
WANT TO HELP? Wondering how you might be able to support the work of Wishes for Elliott?
Resources for
SCN8A Families
Includes:
- Q&A
- Where to Get Help
- Resources
Hear why Gabi
and John decided
to launch
Wishes for Elliott
