The DDX3X Foundation is an international nonprofit organization that aims to find a treatment or cure for DDX3X Syndrome. As parents of children with DDX3X Syndrome, they understand the challenges associated with raising a child with this condition. The foundation supports existing research, education, and treatment programs focused on DDX3X Syndrome.

They have three primary functions: supporting research, connecting families, and raising awareness. The foundation provides resources and support to families navigating this journey through their website and Facebook group. They also organize scientific conferences and family gatherings.

With their mission to connect families, resources, and the medical community, they strive to advance research for a treatment or cure for DDX3X Syndrome. The DDX3X Foundation has had a significant impact, with over 1,000 known cases across 56 countries and over $1. 6 million raised.

They have also awarded over $800,000 in research grants and are a Rare As One Network grantee. The foundation's ultimate goal is to accelerate brain function in individuals affected by DDX3X Syndrome through advances in cell and gene therapy and pharmaceuticals. With dedicated co-founders and a passionate leadership advisory board, the DDX3X Foundation aims to become the leading international foundation for DDX3X Syndrome.

They strive to be a top funder of research and continue building partnerships to drive progress against the disease. By supporting the foundation through donations or participating in their registry, individuals can contribute to their efforts in finding a cure for DDX3X Syndrome