Follow us:

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



Children's Craniofacial Association

13140 Coit Road, Suite 517

Dallas, TX 75240

Toll-free   800.535.3643

Phone       214.570.9099

Fax             214.570.8811


Erica Mossholder, MBA, Executive Director

Erica has served CCA in the past as a Board member and volunteer. She brings her experience from the fields of higher education and business development to CCA to help continue the strong, 26-year legacy of empowering and giving hope to families affected by facial differences. Erica seeks to find new ways to connect our community and help make the world a kinder place.

Charlene Smith, Executive Director Emeritus

Char has been with the charity since its inception, taking over as Executive Director in 1991. During that time she has served in every position and has an intimate knowledge of the day-to-day workings of the charity.

Annie Reeves, Program Director

Annie coordinates CCA’s programs and services (family retreat and scholarships, newsletter, financial assistance, CCA's Yahoo groups and family networking) and communicates directly with the CCA families who contact Children’s Craniofacial Association for assistance.

Jill Patterson, Development Director

Jill manages all areas of fundraising, and oversees CCA-sanctioned events. In addition, she provides guidance to families and friends who want to help Children’s Craniofacial Association by holding fundraisers that benefit CCA Kids. Jill is also the person to contact regarding Web store sales.

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

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