About us >  About VCFS FAQ

Welcome to the Velo-Cardio-Facial Syndrome Foundation of Queensland.

The VCFS Foundation of Queensland is a Brisbane-based families group with members and friends across the Australia and the globe. Our primary purpose is provide support to people with VCFS and their families, but we also:

  • help and support people with VCFS and their families
  • educate the general public about VCFS and how it affects those with the syndrome
  • raise awareness about VCFS
  • lobby and advocate government, medical and educational institutions
  • to promote the interests of VCFS sufferers and their families.

This site provides information on VCFS, the activities and projects of VCFS Queensland, and links to other VCFS sites. If you do not live in Queensland or near Brisbane and need direct assistance or support, visit our Contact page to find a group near you.

The Velo Cardio Facial Syndrome Foundation Queensland was established in 1997 by three families who found each other when their children's diagnoses of VCFS left them confused and searching for information about this unheard of disorder.





Copyright © 2008 Velo Cardio Facial Syndrome Educational Foundation Inc.

International Rare Disease Day

28 February 2010

Family Day pool party

7 March 2010

12 to 4

> More info

Donations