Guest guest Posted October 17, 2009 Report Share Posted October 17, 2009 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 Quote Link to comment Share on other sites More sharing options...
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