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Duration: 1 hour

Jono Lancaster, 26, (featured in BBC3's Love Me Love My Face documentary) has suffered rejection and discrimination his entire life - all because of the way he looks. Born with a rare genetic condition, Treacher-Collins syndrome, Jono has no cheekbones or external ears and has endured years of bullying and countless hospital appointments.

The nature of the condition means that any child Jono fathers will have a 50 per cent chance of contracting Treacher-Collins. Now Jono has an important question he wants answered - what if my baby was born like me?

The film follows Jono and his girlfriend Laura as they go on a quest to find out the options available to them should they decide to start a family. Jono meets a variety of families who have faced or are facing this very conundrum. He also meets with youngsters affected by Treacher-Collins to see if attitudes have changed since his days at school.

Confronted by all the options, what will they decide? And will the decisions they make draw them closer together?

Last on

Wed 24 Aug 2011 02:20 BBC Three

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  • Photo: (l-r) Laura Richards, Jono Lancaster and Maisie

    Photo: (l-r) Laura Richards, Jono Lancaster and Maisie

    Laura Richards and Jono Lancaster meet Maisie, who also has Treacher Collins syndrome.

  • BBC Three Blog: Jono Lancaster

    BBC Three Blog: Jono Lancaster

    "Wow - where do I start? This is all still a bit crazy. A year ago I was a man with the dream to raise awareness for my condition, Treacher Collins Syndrome. Now we're onto the second documentary So What if My Baby is Born Like Me? and the first one, Love Me Love My Face has been shown literally all over the world"

    Read more from Jono Lancaster on the BBC Three Blog


Matt Rudge
Matt Rudge
Matt Rudge
Executive Producer
Fiona Campbell
Executive Producer
Ravinder Chahal


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