Little Faces, Big Hearts is a support group committed to connecting families and individuals affected by VCFS (Velocardiofacial Syndrome/ DiGeorge/22q11) and other genetic disorders. We would like to provide a network for any family or individual with special needs.

 My motivation for creating this group was inspired by my personal experience with my daughter Briley's diagnosis with VCFS.               

The 3rd Annual VCFS Awareness Walk will be held: Saturday, March 2, 2013 @ 9:00am Please message for details!

2012 VCFS Awareness Walk

Connecting Families One Hand at a Time 

Ryan & Jenny Dempster Foundation Awareness Tour 2011 ( My daughters Briley & Lily)