FOXG1 is a key to understanding many brain-related disorders.

We have a running theme throughout our Foundation- 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 is forging breakthroughs with cutting edge research and a formidable strategy to find a cure.

 

322

people diagnosed in the world so far

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$330K

raised for research worldwide

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FOXG1 FACT

the type of mutation the child has plays a large role on his or her developmental skills

More info

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. The newly created project group FOXG1 Research is one of the many projects under the European based Blackswan Foundation and are in no way affiliated with IFF. Funds raised by said groups are not provided to or used by IFF. 

 

 

 

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