Treacher Collins Syndrome is a uncommon genetic situation that impacts the expansion of facial tissues and bones, resulting in impaired respiration, listening to, and imaginative and prescient. Nonetheless, it has no affect on an individual’s intelligence or their skill to really feel the harm of rejection. This situation impacts about 1 in 50,000 individuals at start and might trigger slanted eyes, little eyelashes, and malformed ears.
Jono Lancaster was born with Treacher Collins Syndrome in October 1985, and his mother and father have been knowledgeable by medical doctors that he would probably by no means be capable to stroll or discuss. When he was lower than two days previous, they supplied him up for adoption. Fortuitously, a foster mom named Jean arrived two weeks later and fell in love with him at first sight. She formally adopted him 5 years later, and he has by no means forgotten her affection.
Regardless of the unwavering assist of his adoptive household, Jono struggled to just accept his look and didn’t cease avoiding mirrors till he was in his early 20s. Nonetheless, he has since come a great distance and is now a passionate supporter of these impacted by Treacher Collins. He makes use of his private experiences to talk to teams and colleges all world wide, encouraging self-confidence, positivity, and love for oneself.
Jono is now 32 years previous, has a long-term girlfriend, and is pleased with who he’s and what he has completed. He would not select to have facial reconstruction surgical procedure, as he believes that God created him this manner for a purpose. As an alternative of feeling sorry for himself, he has determined to like the way in which he seems and expose his stunning smile and piercing blue eyes to the world.
To study extra about this wonderful man and his optimistic way of living, watch the BBC documentary “Love Me, Love My Face.” Share his story with others to encourage a optimistic outlook and love for oneself.