33 years ago child was abandoned by his parents for being too ugly, but today he is a famous inspirational teacher!

Childhood years are supposed to be the magical years, but let us suppose your parents reject you at birth because they think you are “too ugly” to be a part of their lives. You would feel sad. Wouldn’t you? This is a true life story of someone who was rejected at birth, but stayed positive.

Jono Lancaster, now 33, has Treacher Collins syndrome—a genetic disorder that affects the facial bones development while in the mother’s womb—there are no cheekbones, so the eyes droop down. Apart from hearing and eating issues, Treacher Collins syndrome sufferers exhibit normal intelligence and develop normally.

Lancaster was abandoned by his parents 36 hours after his birth. He was left at the Social Welfare.  Then a wonderful woman named Jean Lancaster adopted Jono and raised him.

Jono, as a little boy, full of smiles

(Jono Lancaster/Facebook)

When Jono was at school going age, he started to become aware of himself; that he looked different from his classmates. He said they would run away and pull faces at him saying they did not want to catch his ”disease.”

“I used to hide how unhappy I was from my mum. She had already done so much for me,” he told the BBC in an interview.

When Jono was a teenager he really became very rebellious, not because he was a bad person, but because of his pain. He would do things to attract attention and that would deter people from the real problem, his physical features. He used to bribe people with sweets so they would like him. He used to drink a lot.

”I was feeling so alone.”

(Jono Lancaster/Facebook)

 “I was desperate to have friends, I’d do anything. I had no confidence. I’d buy sweets and give them to the other kids so that they’d like me.”

Then came the turning point; when Jono was 19, the manager of a bar that Jono often visited, took interest in him and offered him a job. Jono said that he was so anxious before a shift, he would be dripping with sweat.

“I was so nervous and scared about people’s reactions. Drunk people can be so horrible, so obvious,” he said.  “It wasn’t easy, but at the same time I met so many nice people who were genuinely interested in me and my face.”

In the meantime, he completed a diploma in sports science and a fitness instructors course. Jono found a job in a gym and the people there took an instant liking to him. He said that it was a challenge to him, as gyms have wall to wall mirrors. While working at the gym he met and fell in love with a beautiful woman, Laura. They became inseparable.

Image result for ono Lancaster and his wife, has Treacher Collins Disease
A beautiful couple Jono Lancaster and long time girlfriend Laura. (Jono Lancaster/Facebook)

”I just feel so relaxed in her company,” Jono said  in a BBC interview.

Jono and Laura bought a house together in Normanton, West Yorkshire. The couple have busy lives and Jono now works as a team leader for adults with autism. He believes everything has a reason. Mr. Lancaster is devoted to bringing awareness to the public about Treachers Collins Syndrome, and how to deal with it.

Image result for jono lancaster daughter
“Here’s Mariah who I met in beautiful Perth. Gotta be one of the cutest kids ever!” (Jono Lancaster/Facebook)


Image result for jono lancaster daughter
Jono working with students with Treachers Collins Syndrome. (Credit: Jono Lancaster)

Although his biological parents still refuse to acknowledge him as their son, and it still hurts him, Jono has learned to accept it. He still faces many social challenges, but he is learning that by having a compassionate heart, one can change people’s minds. He was resentful when he was younger, but now he has found himself.

Doctors always ask him if he would like to have some more constructive surgeries, but he has declined them  gracefully,  saying that  God made him this way,  and that he is proud of who he is.

(Jono Lancaster/Facebook)

Jono Lancaster, prince of hope, is actively involved in projects bringing light to Treachers Collins Syndrome and Adult Autism, all over the world.

Today, Jono works as an inspirational teacher, talking about Treacher Collins Syndrome. “My parents still want nothing to do with me,” he says, “What’s changed is my attitude, and that’s what’s so powerful. […] I wouldn’t change any of it. My attitude was more disabling than anything. With the right attitude, you can achieve anything.”
Jono Lancaster is an inspiration to many, he has not let his external appearance dim his inner light.