Welcome to VCFS Texas Incorporated
CHANGING LIVES - EMBRACING HOPE - RAISING AWARENESS
We are a not-for-profit organization dedicated to providing support and resources to individuals with Velo-Cardio-Facial-Syndrome (VCFS) / 22q, their families, professionals, and the community in Texas.
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Educational Resources
Velo-Cardio- Facial-Syndrome (VCFS) Educational Foundation, Inc.
The Foundation is an international not-for-profit organization dedicated to providing support and information to individuals who are affected by Velo-Cardio-Facial syndrome, their families, physicians and other practitioners.
22Q Central - Care to be aware
22q Central is a 501(c)(3) non-profit organization with the goal of promoting awareness and education regarding a common, yet many times overlooked, genetic disorder known as 22q11.2 Deletion Disorder, DiGeorge Syndrome, VCFS (velo-cardio-facial syndrome) and others. Parents
22Q The International 22q11.2 Deletion Syndrome Foundation, Inc. (Music)
22q is a non-profit organization that was founded by parents in an effort to bring awareness and support for this rare and under recognized condition. The organization is built on the belief that through identification, appropriate treatment, research and education there can be a better quality of life for those living with this condition and their families, improved medical care for patients with this condition and one day a cure for the 22q11.2 deletion.
