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!- 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. Max had a short life but Max Appeal is a charity with a vibrant life of its own.
Supporting families affected by DiGeorge Syndrome, VCFS and 22q11.2 deletion.
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Anyone can contact us directly
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15Meriden AvenueWollastonDY8 4QN
https://www.maxappeal.org.uk/