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New Patient of Dr. Goldberg

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Hi Everyone,

I know this is a general question, but I have a 4 1/2 year old son who was born

with congenital CMV. We live in Baton Rouge, LA and have been seeing Dr. Cave,

a well known DAN doctor for the last two years. Though our son has done very

well under her care, we have felt that not addressing his initial virus is a

mistake so we are now going to California to meet with Dr. Goldberg and have a

spect scan run. I know the first time I saw Dr. Cave I had no idea what she was

talking about and felt totally overwhelmed. Since then I have learned A LOT.

If anyone has any general advice on anything I should be doing before our visit

or tips please send them my way. I have been hesitant to add on the expense of

a new doctor and really believed in the DAN protocol so I am feeling like I'm

leaving one church for another. According to Dr. Cave for instance, a lot of

our son's sensory and attention issues are related to metals in his system.

Chelation doesn't seem to be a part of Dr. Goldberg's protocol so I'm feeling a

a bit torn. However, I know his problems all stem from an initial virus and

it's time to get an expert opinion on how to treat this aspect.

Thank you in advance for any advice-

Colleen

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