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Friday, February 23, 2007

Martin's Answer to the Ashley Treatment

A blog begun by a parent of a child with a disability . It reads:

"Our intent is show that extreme measures are not an option. Our child's name is Martin and he has disabilities as severe, if not more so, than Ashley. Martin lives at home, is growing to a normal size and stature, and he will continue to do so without medical intervention to stunt his growth."

and describes the meeting with the AMA this week.

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