We are family. We have a bond that transcends physical ties; one born of countless sleepless nights, through helplessness, tears, and the joy of pure, innocent laughter and smiles. The International FOXG1 Foundation is here to support you with information, resources, and love. Our highly active virtual parent community will help guide you along your child’s journey, while the Foundation supports and connects families, raises awareness in our communities, advocates for FOXG1 Syndrome and educates the public about this rare disorder.

International FOXG1 Foundation is a 501c(3) non-profit corporation registered as the International FOXG1 Foundation. EIN 46-1332092

Disclaimer: The information provided on this website is to inform and help parents cope with the sudden, unexpected change in their life due to a FOXG1 diagnosis. The information contained on this site is not intended to replace information you have received from doctors or other health professionals. We are not doctors, we are parents of children diagnosed with FOXG1. Images cannot be used without express written consent.
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