Becky White was introduced to the Children’s Craniofacial Association in 2007 after her third child was born with Pfeiffer Syndrome, a craniofacial condition. Immediately, through CCA, Becky and her family were connected with other families with similar conditions through which they were able to receive immediate emotional support. The first person they talked to from CCA was Annie, who assured Becky that CCA would be there to help her family as they began their journey into the craniofacial world. From her first retreat, Becky knew that she had to do what every she could to ensure CCA would be there for other families to come and has fundraised for CCA since 2011. Since then, Becky has endeavored to do her part in carrying out the mission to give hope to individuals and families affected by facial differences.