In this video, Ben Figueroa shares what it meant to discover the International FOXP1 Foundation. His words are a reminder of the power of community and the deep connection that unites families around the world on the FOXP1 journey. Special thanks to Claudia Parker for beautifully filming and editing this video!.

A team of researchers at the Seaver Autism Center at the Icahn School of Medicine at Mount Sinai in New York has been providing evaluations and clinical research for families of other genetic syndromes for some time now, and has recently begun working with FOXP1 families. In this RareConnect webinar, we will have a chance to hear from these investigators and to ask them questions about their work, how it could benefit us and their future plans for FOXP1 research. Download the slides and meet other families with FOXP1: https://www.rareconnect.org/en/community/foxp1/article/foxp1-community-webinar

Zoom meeting, January 16, 2022 The International FOXP1 Foundation (IFF) hosted their first Open House zoom meeting, open to all members of the FOXP1 international community.  The Board of Directors presented what has been achieved in the first year of the foundation, and what is planned for the coming year. Questions were answered at the end of the presentation.

Playback: Watch the Seaver team present the Center's clinical and stem cell research on FOXP1 Syndrome with special guest speaker, Dr. Genevieve Konopka, who discusses cell-specific targets in early brain development.

Webinar, July 9, 2022 Chardell Buchanan, registered dietitian nutritionist and coach, shared her advise on how to make it easy to prepare healthy meals and snacks for your family. She talks about importance of a balanced diet with many good tips on how to incorporate whole grains, fibres, omega-3, vitamins and water in your families diet. To learn more about Chardell's dietary tips check out her website www.ChardellBuchanan.com