Get To Know Us Our History

VCFS foundation started many years ago by the families who once looked for some support and better treatment for their kid and other family members. Today, we are one of the largest communities in Australia, supporting thousands of people who have this syndrome. When we started our journey, we only had a couple of volunteers, which has gradually increased over the years and now it is more than 140. Moreover, we have also associated with much more educational and medical institutions in comparison to our early days.

• Our Volunteers
• Our Networking
• Our Events

We want to support and encourage people who have this syndrome. Our community will also try to establish and maintain links with other concerned groups in Queensland and other parts of the country. We also want to support VCFS sufferers and make life easier for them with our constant efforts. Our volunteers want to manage tutorials, seminars, lectures, etc., for sharing, discussing and distributing information regarding this health issue. We also want to plan with governments and health funds to make sure that such people have easy access to funds to get treatment and therapy.

We want to build a community where all the people will get equal opportunity as much as possible, even if a person has Velocardiofacial Syndrome. We want to help every kid and grown-up in Queensland and other parts of the country, who find it difficult to talk, eat, learn and unable to behave properly. As a community, we always want to stand with them in every big or small moment of life.

At VCFS foundation, the objectives are very clear. Within a year, we want to add 50 new volunteers to our team so that we can work in a much more detailed and organised manner. There are still many families who are struggling with this problem and are desperately looking for some solution. We also want to organise more event and to all the possible location in Queensland, so that we can educate more people about it.