Hi, I would love to know more about the disorder called 22q11.2 deletion syndrome because of your foundation, can you tell me if you have information here in this website about that illness?
Hello, we appreciate your curiosity about the 22q11.2 deletion syndrome. Our website currently has a section about this specific syndrome named after the illness itself. It can be found at the top left part of the page. We hope the information here is enough to let you know about this syndrome. If not, you can message us and we’ll give you various links and websites that will give you deeper information about 22q11.2 deletion syndrome.
If I would like to donate, how can I do that? And how can I join the foundation?
Thank you for considering donating, we appreciate your thoughts. If you’d like to donate to us, you can just send us an email regarding the donation. You may also consider visiting us in our foundation which will be much better so we can talk personally. For joining our foundation, kindly send us an email. Just click the contact section in this website.
I’d like to join your foundation and help by playing sports, how can I be a part of the group of athletes who play for your organization?
If you would like to join our foundation and be one of our athletes, please send us a message through emails. We will immediately respond to you and we’re going to need you to fill out forms so you can join us.
Do you help only children with 22q11.2 deletion syndrome or adults as well?
No, we don’t just help children with this syndrome but the adults as well. We also give help for people with other illness, we just focus mainly on 22q11.2 deletion syndrome or DiGeorge syndrome.