For the community
Our diagnoses are rare. Our community is not.
GETA was founded by parents of children with rare genetic epilepsies. We know how it feels to search for answers. Here is where to find the people, events and research that can help.
You’re part of the team
Questions? We’re parents too.
If you can’t find what you need, send us a message. We’ll point you to the right group, researcher or clinician wherever we can.
Contact GETA