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Hi everyone. Just throwing my two cents in here too! Evan is going on 5/14 for

a 24 hr. EEG and then on the 5/28 for a MRI. I had the same concerns and wasn't

sure what to say to the docs. Meaning, I didn't really know how to explain what

I was seeing. But, we went to see his pediatrician and I explained it the best

that I could and she sent us to the pediatric neurologist.

I know there is always the question of insurance and whether or not referrals

are needed and will your carrier cover it and all of that garbage...I've been

there and am still doing that...LOL. But all I can say is, YOU are the best

judge of whether or not there is something wrong with your child. Don't give up

if you think your child is having a problem. There have been times (with an old

pediatrician, not the new one) where I have called the insurance company

directly because the old pediatrician wasn't willing to give a referral. I just

got tired of it and went and got a referral a different way.

Anyway, as I said, just throwing some thoughts in.

Love, prayers and heart hugs,

Debbie (GA), Mom to Evan (4.5 y/o with ToF, RBBB, Autism Spectrum Disorder,

Asthma); (now a whole year old and HH and NT?); and my 3 angel babies

whom I will finally see when God says it's time!

9:1-3

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