VCFS Parent Support Network
The VCFS Parent Support Network is a Greater Wisconsin group for families living with Velocardiofacial Syndrome (VCFS)/22Q Deletion Syndrome that offers:
Networking for children and their parents.
Professionals knowledgeable on subjects concerning school, health, etc.
Conferences and workshops.
Support and resources.
Events are scheduled on a periodic basis. You are welcome to contact any one of the parent leaders listed below for general information, updates and questions about events.
To receive email alerts and/or mailings regarding events, resources, etc., register your contact information by emailing Ms. Angie Turner.
For all other questions, feel free to contact any one of the following parents: