Gavin is our child who seems to know no limits. We are constantly in awe of the amazing boy he is. Not only was Gavin born with a cleft lip and palate, but also a congenital heart defect that required surgery at just 11 days old. With each surgery, we seem to be prepared for the worst, and Gavin seems to sail through recovery like it’s no big deal (mostly). Gavin has developed a passion for aviation and aspires to be a pilot. We are beyond grateful to the Mia Moo foundation for their support through the trials of this cleft journey, thus allowing us to better focus on doing all we can to help Gavin achieve his dreams. We are beyond grateful for your compassion for children and families navigating life with a cleft lip and or palate. Gavins Mom