Oliver’s successes could not be possible without the International FOXP1 Foundation. We are forever grateful for the love, support, and research they provide families like our. Please help us find treatment for FOXP1 by participating or donating. 

The International FOXP1 Foundation is a nonprofit organization committed to building a global community that empowers and supports families and individuals with FOXP1 syndrome, a rare genetic disorder characterized by delays in early motor and language milestones, mild-to-severe intellectual deficits, speech and language impairment and behavior abnormalities, by sharing knowledge, inspiring hope, encouraging research, and raising awareness.

Let us come together to raise awareness for our loved ones with FOXP1 Syndrome. This is a time for us to celebrate their successes and the joys that they bring to our lives, while also teaching our communities about FOXP1 Syndrome.