Imagine IFF the seizures went away. Imagine IFF our children could say "Mom" or "Dad". Imagine IFF they could take steps by themselves. Imagine IFF they could feed themselves. These are the dreams of the many hopeful parents of children with FOXG1. We believe that with dedicated research and funding, these dreams can be realized. This is the goal of the International FOXG1 Foundation.
FOXG1 is a severe neurological condition characterized by seizures, small head size, inability to control body movements, and lack of speech. The majority of our children cannot walk or talk. They cannot feed themselves and they struggle to communicate their most basic needs.
WE ARE THEIR VOICE