From Medical Mystery to Meaningful Advocacy With Erica of CCA
About this episode
Laura speaks with Erica about her journey with a craniofacial difference and the importance of advocacy.
In this episode of Our Forever Smiles, Laura speaks with Erica, Executive Director of the Children's Craniofacial Association, about growing up with an undiagnosed craniofacial difference and finding her voice through advocacy. Erica shares her lived experience navigating surgeries, self-image, and the long road to confidence. Together, they discuss the importance of language, accessibility, parent advocacy, and building inclusive community spaces. This conversation offers perspective, reassurance, and hope for families navigating facial difference at any stage. Links: Buy Us a Coffee FB Support Group CCA
More episodes of Our Forever Smiles with Laura Arroyo
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- A Cleft Lip and Palate Diagnosis with a Rare Genetic Twist
- Bring Smiles Despite Miles: Turning a Cleft Journey Into Global Impact
- No Estamos Solas: Clefts, Comunidad y Recursos de Terapia del habla-lenguaje en Español
- Ava the Brava and Beyond: Advocacy, Representation, and Growing Up With a Cleft
- Mental Health, Motherhood, and a Surprise Cleft Diagnosis
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