MOEBIUS SYNDROME IN THE NEWS
Our friend Elisa Schumacher Relyea--another Moebius hero:
"A MOTHER-of-two has never smiled because a rare condition means she cannot move her face.
Elisa Schumacher Relyea, 42, has Moebius Syndrome – congenital facial paralysis.
She has never been able to smile at her children, or even at her husband Tim, 44, on her wedding day.
Elisa, a public relations consultant from New York, had surgery at 16 to alter her face – including putting gold in her eyelids to help them shut. She joked: “I feel my face looks more positive now.
“I can win in any staring competition and I really wish I played poker because my poker face is incontestable!”
By the way, recently the New York Times in its science section ran a long article about scientific analyses of a smile--physically how it happens, what it means, etc etc etc.
Of course, what the piece did NOT do is consider the possibility of people who cannot smile---but who find other ways to do so, from within. Something to think about, NY Times!
This is a site first of all about Moebius Syndrome. But it is also a site about having a facial difference in general, about living with it, about succeeding, and about life. We'll talk here about things directly related to Moebius Syndrome and facial difference, about things tangentially related to it, and about my comments concerning any and all of it.
Showing posts with label Elisa Schumacher Relyea; New York Times; anatomy of a smile; Moebius Syndrome; facial difference; achievement. Show all posts
Showing posts with label Elisa Schumacher Relyea; New York Times; anatomy of a smile; Moebius Syndrome; facial difference; achievement. Show all posts
Friday, January 28, 2011
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