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The
Foundation

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 have created a repository of information on symptoms, characteristics, and behavior patterns unique to our FOXP1 children, as well as best practices and the therapies that could enhance quality of life.  As the scientific community expands their knowledge on FOXP1, so will our repository of information grow.  Regular on-line events are scheduled to connect members from different corners of the globe, and family gatherings will be organized in the future to bring together members of the FOXP1 community. 

The International FOXP1 Foundation will focus on 4 areas:

Supporting individuals and families affected by FOXP1 syndrome
Communicating to share knowledge, treatments and research of FOXP1 syndrome
Establishing a world-wide registry of children and adults with FOXP1 Syndrome
Supporting research into the treatment and understanding of FOXP1 syndrome
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