top of page
kieran hiking at top.jpg

We are the connection between FOXP1

families and science.


It's our belief that with family support and medical research, every child and adult with FOXP1 syndrome will have the opportunity to reach their full potential and lead a productive and rewarding life. 


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.


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. 

Join us on our adventure of growth and endless possibilities! 

Blue Gradient

FOXP1 Syndrome is now in the Europe PMC


What is the Europe PMC?

It is a global, free database of life science publications.   

PMC provides openly available peer-reviewed scientific research.

How can this help us support our fox child?

Share the link with all your clinical practitioners to help them better treat your child with FOXP1 syndrome.​

Screen Shot 2023-10-11 at


"While there is still so much unknown and no real changes in our day-to-day life with the diagnosis, it was a relief to have an answer and explanation for everything about Joey that had felt "off". It is amazing to feel the support from the other families and to know we are not alone."

bottom of page