Want to know the causes of VCFS in children? You can look up various webinars that focus on the causes of this syndrome. The health experts will explain the factors in detail that led to your or someone you know velocardiofacial syndrome. The detailed and accurate information will help you to deal with the problem in a better manner.
An event that will help you to understand the Syndrome. From its statistics and health issues involving to its treatments and therapies, you will get detailed information about everything during this webinar. If your kids or family members have this issue, then you must attend this event.
Kids, who have Velocardiofacial Syndrome, need a lot of motivation from their parents, siblings and society. Therefore, attend playdates with other kids in your area which is the best way to motivate such kids. The motivation will give them much needed confidence, and that will help them to deal with the challenges.
People with VCFS need help and support from people in Queensland. Therefore, we do thorough research about the Velocardiofacial syndrome in this place. In our upcoming event, we will highlight the findings of this research. It will help you to know how many people have been affected by this syndrome.
Attend a webinar regarding the treatment of this syndrome. In some case, the treatment could be therapies and medicines, while in some cases, surgery remains the only option. During this event, you will get a clear idea about the health issues and their treatment.
Here’s you chance to make a difference by entering our competition for contributing to the platform. Focus on youngsters living with this disease. We already have a lot of contributors, but as we are growing, the platform will require more dedicated volunteers. If you want to join us, attend the competition.
As the syndrome make a negative impact on speech and learning ability, people find it difficult to coordinate with others and thus, their behaviour can be problematic. Through our platform we help highlight the behavioural issues, and give information about webinars to solve these issues.
People with Velocardiofacial Syndrome often find it very challenging to deliver the speech. In this event, our experts will explain the therapies that can be used to improve the condition. If your kids or any other family member is struggling with such a problem, then attend speech therapy.
Kids with Velocardiofacial Syndrome often need surgery, particularly when they have a defect in their heart, a cleft palate, need jaw or ear reconstruction, etc. This webinar will explain how some surgeries can be so crucial. As a community, we always try to coordinate with medical professionals for such treatments.
We all deserve to be happy and healthy, particularly those who struggle in their daily life because of the Velocardiofacial Syndrome. During November, raising awareness can help. So, talk about the ways that can be done to keep people with VCFS happy and healthy all the time.