Re: Fibromyalgia and Multiple Sclerosis

[Guest guest]

Hi - getting through emails here - I found out that my fibromyalgia is actually

Lyme disease, a bacterial infection that inflames nerves and soft tissues. It

also presents as 350 other conditions! Including MS. The bacteria like lipids -

ie the fat cells, and attack the nerves and their sheaths for that. Many people

with MS are turning their symptoms around by treating for the Lyme bacteria. The

Lyme documentary, Under Our Skin, features people who said they presented with

MS symptoms. You could learn more by going to www.lymenet.org and using the

Search box at the top of the page to type in MS or multiple sclerosis and read

the archived threads there. Take care - Robin

Fibromyalgia and Multiple Sclerosis

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?

[Guest guest]

Robin, I thought I read that the bacteria destroys the myelin sheath around the

neurons in the brain? Did I day it right? That was very upsetting to read. But

there is something I read that can stop it. It's just my energy... months and

months of studying thyroid 5 hrs a day when drs were getting me so sick. Then

studying fibro & CFS... when I saw the extensive info on Lyme... I have to tell

you Robin it freaked me out, and that is not an expression I use.

It is so insideous. I read about the borelia and the cork screw shape and what

it gets into and does, not that I can remember it all, and then all the

diffenent antibiotics depending on the infection and co-infections and

individual response... Lyme is one comlicated infection/disease.

I just stay positive as many people like you with it do manage for a lot of yrs

if it doesn't hit neurologically.

There is a youtube video call Eight Ball or Behind the Eight Ball, (something

like that, I posted it on this board with a title called US govt and Lyme or

something)?

Anyway, there is a scientist who worked on a project for the U.S. govt. and with

the camera in her face she says borelia was deliberately developed to infect

countries we are at war with... something like that, another guy or maybe her

too, say that it was put into insects to appear as a natural disease and how it

got spread so bad here is my question. It's worldwide now as you know.

This is not far fetched to me, as I've lived to long to not know she was telling

the truth when I saw her in the video. She gives her name I think. I worked in

certain areas when I was well, just as an exec assist, but what goes on, mostly

we don't know and just get spoon fed what the media is told and so on. This

makes me very angry, as it was totally unecessary. I suppose there is a chance

it's not true, but she identifies herself and the project and what it was

called.

I worked in what we'll call catostrophic prevention and recovery. That's a nice

way to put it. 9/11 and other kind of stuff. So I know we don't hear the half of

it.

I just want to be well. And what gets me is the US govt has tried to minimize

this along with the insurance communtiy for so long, Lyme??? Well we can do one

little test for it and that's it... you scratch my back and I'll scratch yours.

I hope this isn't to out there for you, but when I saw the vid which at first

looks strange, maybe hoaky, but when I saw her, I thought, " Nope, she's telling

the truth " .

Take care,

Jean

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> Hi - getting through emails here - I found out that my fibromyalgia is

actually Lyme disease, a bacterial infection that inflames nerves and soft

tissues. It also presents as 350 other conditions! Including MS. The bacteria

like lipids - ie the fat cells, and attack the nerves and their sheaths for

that. Many people with MS are turning their symptoms around by treating for the

Lyme bacteria. The Lyme documentary, Under Our Skin, features people who said

they presented with MS symptoms. You could learn more by going to

www.lymenet.org and using the Search box at the top of the page to type in MS or

multiple sclerosis and read the archived threads there. Take care - Robin

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> 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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