I got my questions answered yesterday and feel much better. They are treating the Lyme first and the rocephrin was chosen since it has gone into my brain and I have lesions.
Until we start the Rocephrin I am taking 2 500 mg of Amoxicillan 2 times per day and after I complete a week (Friday) I up that to 3x per day. I think she wanted to ease me into this. Then, as soon as I am approved by insurance for the Rocephrin we will start that. The LLMD has seen great things with this protocol with patients where Lyme is in the brain.
The LLMD has actually found in her research that Valtrex also works on EBV.
The hormone issues are going to be addressed my the main LLMD. I have currently been seeing her colleagues. The notes on my chart indicate to wait for the main LLMD to deal with this. But they are dealing with the low vitamin d.
Yes, this LLMD did come recommended by 2 people I know who were very, very sick. One of the women I know was featured in Under Our Skin. And my LLMD was featured in it as well. I was informed by the woman I know that the two docs that the LLMD uses in her practice are good, but not as wonderful as the head LLMD. She warned me to hang in there. I think that is leading to a little frustration.
I also met some people in the waiting room who were so positive about their experience.Especially, one man who had many neurological symptoms and lesions on his brain and they are now gone.