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When you think maybe your problems couldn't be any worse,,,,,,,,,,,,,,,
[youtube]http://www.youtube.com/embed/Lybu_ZEFn6w[/youtube]
The fortitude of her parents to allow this movie to be made public
is a testimony to their character
and the serious lessons they have learned in the past 5 years.
Any men who have an impure obsession with lust,
and an overly prejudiced outlook on their
attraction to beautiful women,
ought to watch this important docuмentary.
Published on Jan 16, 2014
The story of five-year-old Julianna Wetmore, who suffers from an extreme condition called Treacher Collins syndrome.
Julianna Wetmore was born with a rare genetic craniofacial disorder known as Treacher Collins Syndrome. This condition normally appears as elongated or sagging eyes and small or missing ears and generally affects 1 in 10,000.
Not only is this a rare occurrence but, Julianna has perhaps the most severe case ever seen. The condition was first seen during pre-natal scans where doctors thought that she had a cleft palate. However, the full extent of her disfigurement was not seen until she was born.
Treacher Collins Syndrome is a genetic mutation that prevents the proper formation of the skull, cheek and jaw bones. Julianna's case was so severe she required immediate plastic surgery to uncover her left eye and to open up an airway so that she could breathe.
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Topic: Growing Up Without a Face -- Julianna Wetmore (Read 863 times)