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Children's Craniofacial Association is a national, 501(c)3 nonprofit organization, headquartered in Dallas, Texas. Nationally and internationally, CCA addresses the medical, financial, psychosocial, emotional, and educational concerns relating to craniofacial conditions.
Each year, more than 100,000 children are either born with or develop a craniofacial condition. Their parents and families try to understand what syndrome they have and how to help them. While individuals with a facial difference are frequently classified by others as inferior, CCA is changing the narrative and empowering these kids and adults to be self-advocates. We offer family networking, social gatherings, an Annual Family Retreat, direction to and financial assistance for quality medical care, and educational resources for schools and communities to learn the values of tolerance, acceptance, and self-love.
“We appreciate everything Children's Craniofacial Association (CCA) has done for our family. Without the help of CCA we would not have been able to make the multiple trips over 300 miles away to Doernbecher Children's Hospital for our daughter Everly's appointments and surgery. Their financial and emotional support has been such a blessing and relief to us. With the help of CCA, we were able to stay comfortably for multiple nights in a hotel and focus on what was important, the health and recovery of our beautiful daughter, Everly.”