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Re: Re: Fibromyalgia and Multiple Sclerosis

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Hi - I'm not a doctor, so I'm learning as I go here - the bacteria like

lipids and so they attack the fatty myelin sheath around neurons. I also learned

that cholesterol, lecithin and fatty acids, plus proteins, make up the myelin

sheath, and that magnesium is needed for the production of the first three. So

that's another Lyme angle, since magnesium gets depleted in Lyme disease.

I know that people do VitB12 for nerve repair. Many have also had stem cell

injections, which stopped their MS symptoms. There may be other treatments too -

as I said, I'm not a doctor, so have to research, like any of us here, about

what people are trying for repair efforts.

Yes, Lyme is complicated and needs to be studied for what it is, how it operates

in the body, how the body responds, and what people are doing. I call it going

to Lyme school.

Yes, looks like gov'ts worldwide messed with the spirochete. I think it's been

going on for a 100 years, starting with the Japanese, then US, Russia, Germany,

and two more countries I read - forget which ones. Plum Island off the tip of

Long Island was centrally involved here. Some think they mixed brucellosis,

visna virus and mycoplasma - it's a theory, with patents.

We have to stay positive and choose to learn and then plan how to deal with it.

I had a miraculous recovery in one week's time from fibro and joint swelling

when I started the clindamycin. I also treated many other symptoms along the way

when I didn't know I had Lyme. In that way, I'm like you all in that I didn't

know what was going on and so threw things at my body. Some of them worked. But

now I know why - it's the complicated biology of the interplay between the

spirochetal bacteria and the body. - Robin

Fibromyalgia and Multiple Sclerosis

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> Hello, My name is Sharon and I'm wondering if anybody has Fibromyalgia and

Multiple Sclerosis? I have both couples with Post Polo Syndrome and all the

pain symptoms are the same. Can anybody relate to this?

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