Max Appeal....... is all about sharing, about hope and about standing with our families. Our mission is to try to ensure that every person with 22q11.2 deletion lives an independent and prosperous a life as possible. That's not mission impossible! What do we do? * We run events for people of all ages to share experiences, develop and learn. * We provide information and resources. * We provide support to families and individuals to empower them. * We support research to expand knowledge of the condition. * We make it possible for families to talk informally and get together. Max Appeal was founded by parents of children diagnosed with DiGeorge Syndrome/VCFS/22q11.2 deletion. We are a small national charity, run almost exclusively by a group of dedicated volunteers backed up with a knowledgeable panel of medical professionals.

Parent Governor and Chair at a local authority SEN school and college