We found Max Appeal when we got Jack's diagnosis, they've been an invaluable source of help and support  for us and other families in similar situations. 

Max Appeal was founded by parents of children diagnosed with 22q11/DiGeorge Syndrome/VCFS (remove 22q11 deletion syndrome). They are a small national charity, run almost exclusively by a group of dedicated volunteers backed up with a knowledgeable panel of medical professionals. Max, who was the inspiration for their beginning had a short life but Max Appeal is a charity with a vibrant life of its own.

Like many charities, they have found fundraising particularly tough in recent times, so please give generously.

Thank you for your support!