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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Scott Longden

My goal is to complete an Ironman and raise awareness of Velo Cardio Facial Syndrome (VCFS) otherwise known as 22q11.2 DS or DiGeorge Syndrome. Why? You might ask, perhaps the posts on this Blog will explain. Scott Longden's Blog

  

Donate to Scott Longden's Iron Man Challenge


Please feel free to comment or offer feedback. Even better though please donate to the VCFS 22q11 Foundation of Australia.

Caroline Dwyer

Caroline Dwyer is a mother of 3 children . Caroline has a friend who has a child who was diagnosed at 13 years old with VCFS. Due to this fact Caroline is raising awareness and money for the VCFS 22q11 Foundation by doing a 24 Hour treadmill walk for awareness on the 25th August 2011. Hopefully this will help other families get an earlier diagnosis.

 

To support Caroline and her campaign to raise awareness please donate here.


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