Mission >  Projects Committee

 PROJECTS

What we have achieved
Since our establishment in 1997, the VCFS Foundation of Queensland has achieved some major objectives thanks to the support of our members, friends and sponsors:

2002—We held Australia's first international VCFS converence in Brisbane.

2004—We funded an Australian researcher to address the 10th International Scientific Meeting of the Velo-Cardio-Facial Syndrome Educational Foundation (VCFSEF) in Atlanta.

2004—We gained representation on the board of the International Velo-Cardio-Facial Syndrome Educational Foundation.

2005—We opened and continue to fund Australia's only multi-disciplinary centre for the diagnosis, treatment and research of VCFS at the Mater Children's Hospital.

2006—We hosted the 13th International Scientific Meeting of the Velo-Cardio-Facial Syndrome Educational Foundation in Brisbane in partnership with VCFSEF.


What we still need to do

Establish an International Consortium of the world's foremost centres for the diagnosis, treatment and research of VCFS. Target 2008
Create and fund a fellowship that will allow a Queensland medical student to train and study at the best centres in the world. Target 2008
Have VCFS recognised by Medicare and all Australian health funds. Target 2009
Have VCFS recognised as a disability by the Australian education system. Target 2009

Right now? Help us to reach $100,000

Our most urgent priority is the funding of the VCFS Centre at the Mater. With rising allied health costs and the planning for the new Queensland Children’s Hospital (QCH) the Foundation needs $100,000 to bed down the short and medium-term funding for the clinic.

This money is needed for clinic operations to help secure our spot at the new QCH.

Donations are tax deductible

All donations to VCFS Foundation of Queensland are tax deductible. If you are not able join us at the annual fundraisers, you can take up a sponsorship package. Call Steve Russell on 07 3004 8810 or 0418 392 015. Alternatively, click on the button below to learn how to become a sponsor.

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

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