The Velo-Cardio-Facial Syndrome Educational Foundation, Inc. is an organization comprised of both professional and lay people whose purpose is to educate the public, the scientific community, families of individuals with Velo-Cardio-Facial syndrome, and individuals with Velo-Cardio-Facial syndrome (VCF) about this common genetic disorder.

• The Foundation will act as an advocate for both patients with VCF and the professional community treating this disorder.
• The Foundation will provide a forum for the advancement of knowledge relevant to the diagnosis and treatment of individuals with VCF.
• The Foundation will provide a forum for discussion of the problems, treatments, or achievements associated with VCF and its management.

The Foundation is organized divisionally into a number of continental groups, with directors for each part of the world represented on the Foundation's board. These divisions are: