The VCFS and 22q11 Foundation supports families and persons affected by VCFS or Deletion 22q11.
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Latest News

Latest News

2009 Walk for Awareness

The opening of the 2009 Walk for Awareness. Mayor Tony Issa cuts the ribbon

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New VCFS 22q11 Website Launched!

Thursday 25 Feb 2010 - our new Fresh Look website went LIVE!

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VCFS 22q11 Pink and Blue Ball

A fabulous night, with the launch of the 2010 VCFS community service announcement featuring Lisa...

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The VCFS  and 22q11 Foundation Inc. 

The Velo-Cardio-Facial Syndrome  and 22q11 Foundation is a registered charity (INC 9875404).  We have DGR Status and all donations of $2 or more are tax deductible.

The VCFS and 22q11 Foundation are a group that consists of individuals with VCFS, parents, grandparents, siblings and carers of individuals with VCFS and professionals.

The foundation was founded by the late Dr Tony Lipson of the Children’s Hospital Westmead, NSW.  Dr Lipson helped parents establish the first support group in the world for individuals with Velo Cardio Facial Syndrome.  The foundation has been run for many years by countless volunteers who have given their time to help other families also walking this same path.

The VCFS and 22q11 Foundation objectives are:

The VCFS and 22q11 Foundation has:

This graph is to show where our money was spent in 2010/2011. In 2012 we plan to host a family camp/ retreat.


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