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Peer Networking program

Our Peer Networking program bridges the gap between isolation and community by matching families navigating facial differences with others who truly understand the journey. Whether you are seeking comfort and guidance from someone who has walked this path, or you are ready to volunteer as a mentor to lift up a family just starting theirs, this program provides a safe, empathetic space to share experiences, exchange practical advice, and build lifelong friendships. Together, we ensure that no family ever has to navigate their story alone.

I want to connectI want to be a volunteer

Family Networking 

Attend our  annual gathering of families from across the globe. We do offer travel scholarships.
Retreat

Support Groups

Find connection, support, and resources for adults with facial differences and caregivers.
CaregiversAdults & Alumni

CCA Interviews

Explore inspiring interviews, stories, and conversations from the CCA community.
Check All Interviews
Keep the connection going

Partner Organizations Monthly Groups

myFace

myFace runs its own set of online groups for families navigating facial differences a good option if you want an extra touchpoint between CCA events.

Visit myFace groups →
ConnectMed

ConnectMed offers similar peer sessions on a quarterly basis through their Camp Cosmos program.

Visit ConnectMed →
Next session: December
Hear it in their own words

Social Media / YouTube Resources

CCA Interviews

Some of the people with hemifacial microsomia we've interviewed:

CB

Chelsea Buyalos

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RD

Rasheera Dopson

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LD

LaDarius Davis

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Good Influencers to Follow

Creators sharing their journey with facial differences online:

JL

Jono Lancaster

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PD

Peter Dankelson

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IB

Iva Ballou

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AB

Aaliyah Booker

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PB

Paige Billiot

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Children's Craniofacial Association
Supporting and inspiring individuals and families affected by facial differences since 1989.
15851 Dallas Pkwy. Ste. 245, Addison, TX 75001
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214-570-9099
Toll-free at 800-535-3643
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