Guest guest Posted September 4, 2010 Report Share Posted September 4, 2010 I was looking over old messages and found one from Rich who said he had the idea that one would have difficulty getting cellular magnesium up to decent levels as long as glutathione levels were low. It was just a passing comment, on some other related topic. Does anyone have any more thoughts on this? , my daughter, is being treated for Lyme Disease as part of her CFS constellation- quite successfully at last. The turning point was starting IV rocephin along with Valtrex. Valtrex alone made no difference, but together with the rocephin, it is like magic. She was getting weekly Magnesium and Vitamin C IV's alternating with lipid/glutathione IV's (for about 10 months) and this stopped her muscle twitching. Unfortunately we can't afford these any more and have changed to nebulizing glutathione/B12 and oral liposomal magnesium. Things are still pretty good (she's been doing the nebulizing/oral Mg for about 2 months now)but her eyes have started twitching again. I'm worried that she might be depleting the stores she built up and wondered if anyone knew any more about this glutathione/magnesium connection Rich was thinking about. She's tried adding in magnesium cream in the past and epsom salt baths with no success in stopping the twitching. She's going to up the oral liposomal Mg but her doctor doesn't know what the upper limit would be. Because it is liposomal, there is no bowel tolerance like there is with straight oral ( which she can't take very much of for that very reason) so he is a bit concerned about Mg toxicity. Anyone have any experience with this area? Thanks Quote Link to comment Share on other sites More sharing options...
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