If your child or loved one has just received a craniofacial diagnosis or experienced a facial trauma, we know you have questions. The Craniofacial Foundation of America exists to help families just like yours.
Whether you're wondering what's ahead for your child with a cleft lip or palate, would like to know the treatment plan for a craniofacial birth defect, or need to make an educated decision about care after a traumatic facial injury, we have answers for you.
The Craniofacial Foundation of America (CFA) is a nonprofit organization dedicated to improving the lives of patients with facial differences.
The foundation offers a variety of services to patients, their families, the public and health care professionals. These services include:
- Coverage of non medical expenses such as mileage reimbursement, food and lodging
- Support services like parent to parent networking and events for patients and their families
- Educational resources and materials to help parents better understand possible care options