We help kids as well as grown-ups who are suffering from Velocardiofacial Syndrome. Whether it is a clinical requirement, educational requirement or any other type of support, our volunteers are always ready. We leave no stone unturned to make sure they live a happy and healthy life.
We also aim to raise awareness about Velocardiofacial Syndrome and educate people about it. We also give advice to the government, educational and medical institutions to uphold the interests of people having his syndrome and their families. We try our level best to make their life a little easier.
Our foundation also takes part in various researches regarding the Velocardiofacial Syndrome in Queensland and other parts of the country. We consult with international experts on this matter to find innovative ways to help every individual. We use the finding of our research to educate the people.
There are many VCFS Clinics in Queensland that provide medical service to children and young people who are suffering from this syndrome. Our foundation provides support to such clinics in more than many ways.
Everyone deserves to lead a happy and healthy life, even if they have Velocardiofacial Syndrome. Our foundation makes untiring efforts so that kids and young people with this syndrome can get all sorts of medical help and other services. The health issues that are part of this condition may vary from child to child. These health issues include cleft palate, heart defects, weak immune against infection, low calcium levels, kidneys issues, characteristic facial appearance, learning, speech and feeding difficulties. We understand the seriousness of these conditions and thus closely work with the health department to improve their condition.
We are organising an event in Brisbane city that will focus on the basic understanding of the Velocardiofacial Syndrome. If you want to help your kids, family members or a friend, who has this Syndrome, you need to have some knowledge about it. Our expert will explain the Syndrome in the simplest way.
Treatments are available for people suffering from Velocardiofacial Syndrome, but the treatment will be based on the type of symptom. In some case, supplements are enough, while in other case, surgeries become essential. We are organising an event in Sunshine Coast in this context.
Any kind of syndrome is a result of a genetic disorder. Therefore, it is essential to know about it. In our upcoming event that we are organising for the people of Gold Coast, we will focus on this particular subject. Our knowledgeable experts will explain how about the genetic disorder and Velocardiofacial syndrome.
When a person is suffering from Velocardiofacial syndrome, various health issues can occur. However, surgery is not required all the time. If you want to know when exactly VCFS sufferers need surgery, then you should attend our event that we are organising in Sunshine Coast.
Kids and grown-ups who are suffering from this syndrome should stay physically active. We are organising an event in Brisbane City, where our health experts will explain how its help. They will also emphasise on the type of activities a person should follow.
People with VCFS face various difficulties in their daily life that includes learning problems feeding, and speech problems. If you want to help a person, then you need to know the correct approach. In our upcoming event that we will organise in Gold Coast, we will focus on this issue.
VCFS foundation works relentlessly for the development of kids and grown-ups with Velocardiofacial syndrome. We work throughout Queensland and cover places like Brisbane, Gold Coast and Sunshine Coast. No matter what goals you have, what your dreams and hopes are, we will always be there for you in every step of life. From medical treatment and providing speech, feeding and learning therapies to educating people and raising awareness, we try to help a person in every possible manner.
In order to educate the parents and other family members of people who have this syndrome, we frequently organise various events. After attending the events, you will understand the problem of Velocardiofacial syndrome and the health issues related to it. You will get to know about the treatments, the requirement of such people, the difficulties they face and ways to improve their lifestyle. We organise the events in various places in Queensland.
We are backed by a team of volunteers who make every possible effort to help people with the syndrome. Our volunteers are qualified, and most of them are directly or indirectly linked with the medical industry. So, they understand the significance of providing the right treatment and therapies to such people. We have more than 140 volunteers who are from different parts of Queensland but working together to elevate the condition of kids and grown-ups with this syndrome.
We have successfully helped many people with the syndrome because we have a strong and extensive network. We are closely associated with various government, educational and medical institutions in places like Brisbane, Gold Coast and Sunshine Coast so that we can promote the interests of people suffering from this health issue and their families. Because of our excellent network, we successfully provide these people with what they require at the right time.
Thomas is working with our foundation for its last many years and help by understanding the mental states of such people and their behaviour.
Emily is a social activist and working with the VCFS foundation for last many years. She coordinates with medical, educational and government institutions.
Jack is also a social activist who keeps track of people who have this syndrome and need any kind of help or support from our foundation.
Grace is with us from our initial days, and she helps kids and grown-ups who have this problem and find it difficult to talk.
If you want to help the people who are suffering from Velocardiofacial syndrome, then you can join our community. As we are extending our hands to more and more people in need, we need the help of volunteers. If you believe that you have the intention and ability and enough time to do something good for these people, then you have become a part of this community. You can become our part in three simple and easy ways.
In this event, our experts explained the effect of Velocardiofacial syndrome in our country and how things can improve in future.
“I would like to thank the VCFS community for helping our 8-year-old son. As he has this syndrome, it was difficult for him to talk and learn new things, but VCFS changed everything.”
“My brother has Velocardiofacial syndrome, and thus he always had some behavioural issues and not very social. Then I came to know about the VCFS community, and they help him a lot.”
“I am social activists and work in the Brisbane region. While doing a survey on Velocardiofacial syndrome in Brisbane, I came to know about the VCFS and learn how commendable their job they are doing.”
My 5-year old son has this problem for a long time, and we were looking for the right help. Then someone told me about the VCFS. They helped my son in more than many ways.
People with this syndrome often have heart defects, a cleft palate, etc. We provide the best treatment to such people.
We offer information about therapies that can help the kids to learn and understand in a better way.
This syndrome also causes speech problem in kids. How community help such kids with their speech.
Social behaviour is also a problem with such people; we know the best ways to change things properly.
