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Hello Everybody,

We started thinking our son couldn't hear in November of last year.

We had an ABR and he was diagnosed with profound hearing loss in both

ears. We had an MRI to check out his audidtory nerve and the doc saw

" irregularties in the brain " we went back for our second MRI on

Wednsday and spent the entire day at the Hopital and have now been

told that our son has bihemispheric PMG, he also has a very small

corpus collosum. we still haven't found the reason for the hearing

loss, anyone out there with a child who has this as well? He has

never had a seisure, is that normal, might he escape that? He is

hitting most of his normal growth and devolopment milestones for an

18 month old, he is 15 months old right now. He laughs he play's, he

is so happy. He seems so normal, except that he can't speak, but I

think that is the hearing, well I know it is, he makes sound, he wags

his tongue side to side, he doesn't really drool. He understand's so

many games we play. Is that normal? Do things he can't do start

popping up more as he gets older? Why can't I find bihemispheric PMG

is that the same as something else? What do I need to ask my Doc? I

hope this isn't to long, I have more questions, so many, but I will

wait and see what you all have to tell me.

Thanks,

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