Her parents were told that she had no eyes, no ears and she had clubbed feet when she was first born. The doctors said she would never walk, talk or see. She was born with Treacher Collins Syndrome, a genetic defect that causes facial disfigurement and affects one in 10,000 people. Today, she is a shining example of how to exist and thrive in a world that often defines us by our differences, writes LAUREN TERRAZZANO.
 |
Susan Roesler at work teaching mentally disabled children. |
Already a subscriber? Log in.
Limited time offer:
Just RM5 per month.
Cancel anytime. No ads. Auto-renewal. Unlimited access to the web and app. Personalised features. Members rewards.
Follow us on our official WhatsApp channel for breaking news alerts and key updates!
