Families worldwide
Our community brings together people affected by this rare neurological disorder.
International FOXG1 Foundation
Raising awareness, building community, and supporting families affected by FOXG1 syndrome.
Our community brings together people affected by this rare neurological disorder.
Every contribution helps move understanding and treatment options forward.
The type of genetic change can influence a child’s developmental profile.
We are stronger together
From the first questions after diagnosis through the everyday realities of care, the Foundation connects families to practical information, peer support, and a global community.
Explore resources
Learn how the FOXG1 community supports researchers and studies.
Explore research → CommunityShare your time, voice, or fundraiser with the global FOXG1 family.
Get involved → Give hopeYour gift supports connection, advocacy, and the search for treatments.
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