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As many of you know, baby Dean surprisingly arrived to us last July with an incomplete cleft lip. The Foundation for Faces is the first organization ( aside from the cleft team at BCH) that reached out to us. We participated in the walk last August when Dean was still very young. It was an amazing experience for Kevin and I as parents as we had the opportunity to meet a whole community of families that knew what we were feeling and what we would be going through medically over the next year. Later in 2014 Dean was diagnosed with craniosynostosis which also required surgery and for which he continues to receive helmet therapy. This foundation not only supports children but the families as well. The Foundation for Faces has worked to create a network of support from infancy all of the way up to adulthood. Please help continue to support our family and many more.