*FOXG1Research

It is the mission of the FOXG1 Research Foundation to accelerate research to find a cure for FOXG1 Syndrome.

Led by parents of children with FOXG1 syndrome, The FOXG1 Research Foundation is pioneering ground-breaking research on FOXG1 syndrome, a severe genetic neurological disorder impacting children worldwide.

The organization is dedicated to finding a cure for all children with FOXG1 Syndrome by investing in research, maintaining a strategic roadmap to a cure with the world's most saught-after scientists in gene and drug therapy, and by continuing to uncover the links between FOXG1 and related genetic disorders and related brain disorders such as autism, Alzheimers, brain cancers and more that affect millions of people across the globe.

FOXG1 Research has already found tremendous success by raising its first million dollars in only four months and placing within the top 1% of patient advocacy groups vying for biotech investment. The near-term goal is to raise another million dollars in 2019 to get to clinical trials.

A cure is possible.

Donate to the FOXG1 Research Foundation today so they can continue their outstanding research efforts!