Cleft Awareness Foundation

This organization offers 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. 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. If you are interested in taking part or have resources to share please contact us. Thank you! Facebook: FB.com/CleftAwareness Twitter: @CleftAwareness Cleft Awareness Gear: www.cafepress.com/CleftAwareness