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Empowering and giving hope to individuals and families affected by facial differences

Financial Assistance

Do you travel to receive quality medical care?

If you do, and need financial help, CCA has a

financial assistance program that will help with food, travel and/or lodging. All we ask is that you apply at least four to six weeks prior to your next appointment. For more information, please contact Annie Reeves at 800-535-3643 or by

e-mail, areeves@ccakids.com.

Testimonials

 

My husband and I had our beautiful little girl Averi, but we felt like something was missing. We decided, as many couples do, to add another child to our family. We anxiously waited to find out the sex of our baby after we announced our pregnancy.

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CCA has been an incredible blessing to our family. Our son, Bauer, was born with an incomplete bilateral cleft lip and cleft palate. He has had both his lip and palate successfully repaired. As our journey began...

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Our 10-month-old son, Keegan, recently had surgery to correct metopic craniosynostosis. We live in a rural area in eastern Oregon, where seeing a specialist is a three- to four-hour drive, especially in the winter time...

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Our daughter, Lacey, who was adopted from China, was born without the left side of her nose.  We decided Dr. Genecov in Dallas would be the plastic surgeon to help us, and CCA helped make it happen.

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Livie was born on September 25, 2010, after a very long and difficult delivery. She was bruised badly from her nose up, and her head was not exactly round after her delivery. Because of complications with her delivery, we were back at the doctor’s office frequently after she was born.  Read more...

 

Rosemary was born on Labor Day in 2009 (September 7) at our home in Midlothian, Virginia. She is our fourth child. As soon as she was born, we knew immediately that something was just not right, so we quickly worked on a plan with our midwife to seek further medical care for our daughter.

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I remember it like it was yesterday, I was 30 weeks pregnant with my 2nd child and just had a specialty 3-D ultrasound which discovered she would be born with a cleft lip and palate. I had never known anyone with any facial difference and went through about every emotion possible in the coming weeks.

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13140 Coit Road • Suite 517 • Dallas, TX 75240  |  Toll-free 800.535.3643 • Phone 214.570.9099 • Fax 214.570.8811  |  Email contactCCA@ccakids.com

Children's Craniofacial Association
is a national, 501(c)3 nonprofit organization, headquartered in Dallas, Texas. CCA's mission is to empower and give hope to individuals and families affected by facial differences. Nationally and internationally, CCA addresses the medical, financial, psychosocial, emotional, and educational concerns relating to craniofacial conditions.

© 2016 Children's Craniofacial Association