Dear Charmed3862,
I am also the parent of a child who has ACC. He is completely missing his corpus callosum and he was diagnosed with ACC when he was four months old. He is 16 years old now.
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I am happy to share the information I have learned about ACC while dealing with my son's medical doctors and specialists.
I hope that you and your daughter are doing well.
Sandie
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Originally Posted by Charmed3862
My daughter was diagnosed with Agenesis of the Corpus Callosum... Are there any other parents who's children have the same diagnosis and wish to speak to someone about? I don't have alot of information and wish to find out more... Thanks...
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