Our mission is to build a global community that empowers and supports families and individuals with FOXP1 syndrome by sharing knowledge, inspiring hope, encouraging research, and raising awareness. The International FOXP1 Foundation is a registered non-profit organization that is managed and staffed by parent volunteers. We are committed to supporting those who have been impacted by a FOXP1 diagnosis and to establishing regular venues for fundraising in an effort to further research into FOXP1 syndrome and possible treatments. We aim to "create a future with endless possibilities" because we know there are no limits for our children. We have witnessed our FOXP1 kids talk, walk, run, bike, fish, ski, hike, and more. They are wonderful brothers, sisters, daughters, sons, friends, students, and teammates. Everyday, our kids teach us how to have patience, to show tolerance, to be sensitive, to accept differences and to be thankful for every milestone.