This group is by far the best community of parents I have met that are educated about Cleft Lip and Cleft Palate. BUT, not only are they educated, there is a feeling of community - a true sense of love and compassion that you feel not only with the executives but the community as a whole. I found this group when I was pregnant with my first. It was a great place for me to express my feelings and ask questions to others that I didn't necessarily want my family or friends to know about. Sometimes it is tough to talk about what it feels like to know your children will be born differently. This group allows you to open up and openly discuss with others. They are totally accepting. It's a great group to be a part of!
My son was born with a bi-lateral cleft lip and palate and my wife and I were at a loss in regards to what should we do and how this can happen. Through the foundation, we have received the support and education that is just what the doctor ordered. The foundation is fantastic!!!