My daughter was diagnosed with FOXG1 in 2013. Since finding the International FOXG1 Foundation I've been able to learn more about FOXG1, how to help my daughter with her daily living, and meet clinicians and researchers around the world. I've been fortunate to meet other families and spend time with them, creating a bond that can only be established with others that understand our life. Without the International FOXG1 Foundation's dedication to families and research, our family would be lost in a sea of the unknown. I look forward to continuing the work the founding Board Members started in 2012.