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.
• Family get-togethers.
• 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:

• Jenny
• Amy Vervelde
• Jackie Hribernik
• Deborah Briggs