Why these abnormally facial features?

A Florida girl’s rare disability



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http://www.foxnews.com/health/2012/11/26/florida-girl-with-rare-disability-to-get-surgery/

Thats so sad, Hopefully the surgeries would take care of things at least to some extent...all the best to Katie and her parents ..

I have seen such kind of disorder for the first time. To improve, surgery is the only option. Still, doctor has not confirmed to do surgery.

This is manufacturing defect. So, don't claim that God makes no mistakes. (Incidentally, I do not believe in God and hence will never blame him)

All said and done one must admire the parents who went ahead and had the child in spite of knowing the deformity before birth. Once you see your little baby growing inside you, little deformities don't diminish your love for it , is clear from this incident.I sincerely hope that the child will be able to get back some normality in its features so that it can carry on like other people...

All said and done one must admire the parents who went ahead and had the child in spite of knowing the deformity before birth. Once you see your little baby growing inside you, little deformities don't diminish your love for it , is clear from this incident.I sincerely hope that the child will be able to get back some normality in its features so that it can carry on like other people...

Only a mother can understand and feel that kind of love. I too hope the baby would be normal soon.

I haven't seen such type of deformity before.. she is so sweet even than. I think the parents should continue loving her as love gives her support and confidence even after surgery.

Oh that's sad to see how the kid is suffering from the defect. May be her mother knows the pain though I feel in today's scenario she can be treated well hope she gets fine soon. :)