The foundation promotes education involving early warning signs and accurate diagnosis of genetic vision disorders. It maintains an informative website and publishes a bi-annual newsletter where medical practitioners, scientists, the general public and families and individuals affected by these conditions can find information and research updates.  Hundreds of families throughout the world have joined the VOC Family Network, enabling contact with other families and individuals in their geographic region to share experiences, frustrations and successes involving hereditary vision disorders. Members of the Network, along with the general public, are invited to attend the World Symposium on Ocular Albinism. The Vision of Children Foundation fulfills an important educational role serving as a world recognized information resource on childhood hereditary blindness and vision disorders.