My great-niece, Marley, was born with a condition called FoxP1 Syndrome, a rare genetic neurodevelopmental disorder caused by mutations in the FoxP1 gene, leading to developmental delays, speech impairments, and behavioral challenges.  There is no cure for FoxP1 Syndrome. Currently, management focuses on supportive therapies to improve quality of life.  International FoxP1 Foundation research and support is ongoing.

Thank you for supporting this wonderful cause. Every step you take, every dollar you raise, and every story you share helps advance research, provide resources, and strengthen the FOXP1 community worldwide.