My Rare Facial Deformity Nearly Ruined My Life

Cynthia Murphy, born with Treacher Collins Syndrome, faced a challenging childhood marked by bullying and numerous surgeries. Despite these hardships, she found love and support in her husband, which helped her gain confidence. Cynthia now advocates for craniofacial disorders, running an online community and lifestyle app to support others. Her journey highlights the power of love, community, and self-acceptance.

What new insight or understanding did you gain from this video?