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 is Treacher Collins Syndrome primarily characterized by?

• Resulting in vision impairment

• Leading to hair loss

• Causing skin rashes

• Affecting the facial bones and tissues

How did Cynthia's husband influence her life?

• He encouraged her to move to a new city

• He helped her gain confidence and self-worth

• He introduced her to a new career

• He taught her a new language

What role does social media play in Cynthia's advocacy work?

• It helps in organizing offline events

• It provides a platform for awareness and support

• It is used for fundraising activities

• It offers medical advice and consultations

What did Cynthia establish to support others with Treacher Collins Syndrome?

• A medical research fund

• A lifestyle app and online community

• A physical therapy center

• A series of educational books

What was a significant turning point for Cynthia in accepting herself?

• Starting her advocacy work at age 30

• Completing her education

• Moving to a new country

• Writing a book about her experiences