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Hi, all. The Lou Gehrig's-type symptoms are really amping up, not only from being in a high EMR apartment, but also from the LD treatment w/ Byron White's A-L Complex. I can take a ton of A-Bart & A-Babs at this point, & not notice a thing, so that's led me to figure out that my Lyme load is really high, & the other stuff probably wasn't as big a deal. Sometimes when I take the A_L Complex, I get this really intense burning in the back of my neck (I was bitten at 7 yrs. old right near my occiputal lobe), & it feels like 500 degrees on back of neck. Not sure if that's when I should take a detox bath? When the die off symptoms really amp up? I've been doing the thing where I just take the bath at nite before bed, so that the magnesium & baking soda stay on my skin & continue to draw out toxins as I sleep. But maybe I should, instead, take the bath maybe an hour after taking the A-L Complex, when all the underlying symptoms start to get unearthed (lungs
burning, cranial nerve damage, heart burning, aching & strangling feeling). Also, confession: I can't handle a bath every day. It makes me so nauesous & burning & brings out all kinds of nerve damage in neck & cranial nerves, that prevents me from swallowing reflexively, & holding my head & neck up. I am terrified, & want to do this right. Guess I'm going to have to order a bottle of A-L Complex every month for the next 2 years or so, since I know it works,however terrifying the die-off stuff is. I think it will be wise to double dose it b/c of the strong ALS & endocarditis history in my family, & since docs w/ Lyme-induced ALS always double dose their Lyme abx, for long periods of time, like years. Hello, medicine. So long, food. :( Thanks for your ideas & suggestions.
Love & blessings,
Elysia
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