Max Appeal - Family support services

What we do

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.

Who do we support

Supporting families affected by DiGeorge Syndrome, VCFS and 22q11.2 deletion.

Is there a charge to use this service?


Can anyone use this service?

Anyone can contact us directly

Service details for this family support services

Language: English only

  • Can provide specialist support for families of children with disabilities / additional needs Yes Please contact to discuss your child(s) needs further.
  • Relevant staff have a valid current DBS? No


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Meriden Avenue

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