Every resource is designed for real people living this journey. Every program is meant to take you from just surviving to fully thriving.
Our Peer Networking program bridges the gap between isolation and community.
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CCA provides financial assistance to help families travel to craniofacial specialists.
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If your child is having surgery or going through a hard time, use the link below to request a care package sent to your home.
Request a Care Package
Three days of connection, education, and joy for children, siblings, parents, and adults with facial differences.
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The CCA’s Speakers’ Bureau is a group of trained individuals available to speak in person or virtually to your group.
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CCA provides digital and hard copy literature to share with your school, team, group, family, and community.
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Speakers and stories from families, adults, and donors who have walked this road provide community, strength, and hope in CCA Kids.
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Craniofacial Acceptance Month is celebrated every September. Learn more about how you can share and celebrate in your local community.
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CCA offers PDF overviews of common challenges faced along the craniofacial lifespan. Read more about preventing bullying, what to pack for surgery, and more.
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CCA offers a library of syndrome booklets, written in plain language, to help you understand and share information about common craniofacial syndromes.
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Our newsletter, the CCA Network is published to inform readers of CCA activities, introduce families and connect them, as well as educate families.
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Check out our curated list of books about living with a facial difference based on reading level.
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The David Roche Award for Excellence in Advocacy is an annual award bestowed on a speaker, educator, storyteller, artist, medical professional, or family member in the facial difference community who has gone above and beyond to advance the status of people with facial differences, promote acceptance and appreciation of appearance diversity, and challenged the stigma that surrounds physical differences.
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