VCFS Texas Inc. is a 501(c)(3), non-profit organization formed in 2009. We have created this list to share information about Velo-cardio-facial Syndrome a.k.a DiGeorge Syndrome or 22q11.2 Deletion Syndrome ("VCFS") in Texas. This group is a place to post questions you may have about doctors, therapists, what works, what doesn’t with children with VCFS and to share information about resources available in the community, as well as opportunities to make a difference in the lives of people affected by VCFS. We are inviting folks from throughout the state to join. The idea here is there may be someone who has a relevant experience to share. Tambien se habla espanol!