Here is an interesting read:
http://www.lymebook.com/marshall-protocol
Don't expect to understand it right away...you might have to read it over and over during a few days. It is quite complex.
You can Google the Marshall Protocol yourself and read more.
This is controversial, and some doctors don't believe it.
The RX version of Vit D is D2 and not active in the body. I am unclear about using Vit D in Lyme patients. In sarcoidosis where the Marshall Protocol is used, Vit D is deliberately kept low.
I don't understand the rationale of giving any Vit D if the Marshall Protocol is being followed.
We have a poster here LizaJane... she has had Lyme treatments.
She is on PN.
This is one of her posts. You might want to PM her.
http://neurotalk.psychcentral.com/sh...highlight=Lyme
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All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei
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Weezie looking at petunias 8.25.2017
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