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Supporting people with 22q11.2 Deletion or 22q11.2 Duplication Syndrome.
Awareness, Education, Community & Support
Celebrating 30 years
Contact Us
The 22q Foundation Australia & New Zealand board & committee
is made up of people who have children with 22q
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The 22q contacts are there to provide information on the services available in your area. The contacts are all volunteers. These contacts are not medical professionals. The contact points are not intended to provide medical advice. The VCFS & 22q11 Foundation does not accept any responsibility for advice or information provided by the contacts. It is strongly recommended that persons wishing to use information supplied by the representatives first consult their medical practitioner.
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