Full Website Coming Soon!



Our daughter Ella was born on November 26, 2008 with a unilateral cleft lip and palate. After going through some difficult operations and a lot of uncertainty, we felt it was important to help others that are going through or will go through the same things - and Cleft Awareness Foundation was born.

This website will offer resources, stories, insurance tips, and other good stuff for people looking for answers. Our goal is to create a network of families to help support each other and offer advice. Eventually as we grow we would like to raise money and take donations to help children and families in need.

If you are interested in taking part or you have resources to share please contact us or join us on Facebook. Thank you!

Read more of Ella's Story.