Join Carly in this mission to raise funds for FoxG1 syndrome research and support. FoxG1 syndrome is a rare and devastating genetic disorder that affects children's neurological development. With your generous contributions, we can make a significant impact by funding crucial research to better understand the syndrome, improve diagnostic tools, and develop potential treatments. Together, we can bring hope and progress to Carly & those affected by this condition as well. Please donate today and help us make a difference in the lives of these extraordinary children and their families.