Advancing Research
Empowering Families
FOXP1 syndrome is 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.
The International FOXP1 Foundation is committed to building a global community that empowers and supports families and individuals with FOXP1 syndrome by sharing knowledge, inspiring hope, encouraging research, and raising awareness.
"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."
JOIN THE FOXP1 FAMILY
By joining the International FOXP1 Foundation, you become part of a movement focused on advocacy, research, and support for patients and families affected by FOXP1 syndrome. Together, we can amplify our voices, share hope, and drive meaningful change. Whether you're a caregiver, researcher, or supporter, your involvement is vital in helping us create a brighter future for those living with FOXP1 syndrome.
