Jono Lancaster suffers from the rare genetic defect Treacher Collins Syndrome. It occurs in about 1 in 50,000 newborns. Watch the video to see how Jono copes with his life with the disease and inspires others in the process.

Despite his looks, Jono Lancaster isn’t hiding. Treacher Collins syndrome disfigures his face. But he goes out with friends and even dates on Tinder. “Dating sucks,” says Collins in the report. He always thought it was just because he looked like it. “But the truth is, dating bugs us all.”

Treacher Collins Syndrome: Jono Lancaster’s Journey From Bully Victim To Model

The 37-year-old definitely has a sense of humor. But that’s not all. In 2012, Jono was the torch bearer at the Olympic Games in London. He appears in magazine articles and gives lectures. And he is a well-known influencer. He has hundreds of thousands of followers on Instagram, TikTok and Facebook and countless fans in real life. Jono hasn’t just settled for his looks. He celebrates it, does good things and even earns money with it.

The original of this post “Parents left him as a baby – that’s how Jono is today” comes from glomex.


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