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hi.

my daughter who turned 16 mos old yesterday, was given a diagnosis of

mitochondrial disease. she had a muscle biopsy 7 weeks ago while she

was in the hospital for seizures. dr shoffner read the muscle biopsy.

i am very very new to all of this stuff, the computer, this disease,

what to expect. i would really like some input from other people. we

live close to knoxville,tn and i dont know anyone with this disease

or heard of it. karlee beth has lost her vision in the last couple of

days. we go to the hospital at 645am for egd and ph probe to

determine what kind of feeding tube she needs. her neuro started her

on carnitor today. she weighs 19lbs and 30inches long, she has great

days where she will drink 21-240z of pediasure a day then the next

day she drinks 5-8oz. she has never ever cried to nurse or drink a

bottle. she is not sitting, crawling or talking and still takes a

bottle from me. she is beautiful and such an angel. the neuro told me

he was so surprised of how happy she is. i would appreciatte any

comments from anyone. i have a wonderful husband a 2 other beautiful

children ages 8 and 3.

thanks so much!! this has been a very very sad day for us!

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