Cynthia is a Graduate Student and Craniofacial Awareness Advocate born with Treacher Collins Syndrome. She currently works as a health and wellness activist with her husband through their FREE charity app Assuaged. The Murphys are passionately seeking to bridge the gap between healthcare and self-care to meet the needs of healthy living as a method for longevity. They are going beyond charity and unifying people through love and compassion.
Sunday, November 26, 2017
Kids with craniofacial conditions hope film 'Wonder' will nurture awareness in others
Yates, of East Garfield Park, was born with a particularly severe case of Treacher Collins Syndrome, a #craniofacial disorder, which rendered him unable to open his mouth more than a sliver until two rounds of intense surgery in the last year at Rush University Medical Center. Since then, the Young Magnet High School senior has eaten food for the first time after subsisting on the meal replacement drink Ensure for much of his life. He is able to breathe better and is learning to speak more clearly.
http://www.chicagotribune.com/news/local/ct-met-wonder-facial-conditions-20171115-story.html
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