Re: RE: Burning skin/TO/ CRICKET

July 6, 2004

I was tested for peripheral neuropathy also, and it was not present, but I

had another test, one that is seldom done, and i cannot remember what it

was called, and it found very fine neurological damage. And I definitely

have it.

Lynda

At 11:05 PM 7/5/2004, you wrote:

> Hey there Cricket. How are you? I read your post about the burning

>skin. I have that also, although I have not had that in a few months.

>I do not have perepherial neropothy(sp?) . I have been tested for

>that. For me, it is just part of the Fibro flares. I know what you

>mean by it feels like the skin is on 'fire'. Sometimes the pain comes

>with the burning, but other times, the burning is just by itself.

>Strange, huh? I get the burning on my scalp too! I have read on

>other message boards/Fibro boards/ that other woman have this crazy

>symptom too. I am not sure what it can be except for what someone

>said in an earlier post that it can just be a flare up of some kind,

>and may come and go. Hopefully it just goes. Have you been detoxing.

>Ever scince I did those 2, 3day juice fasts with enemas, my health

>has turned around alot for the better(and the warm wheather helps

>too!) I am planning to do another one next week. Now if I could just

>stop this hair loss, and the yeast problem, I can deal with the rest.

>Peace, hugs, and health to you always. TERRY

>

July 6, 2004

Hi Cricket:

I think Terry is correct b/c I read about burning with FMS. Rogene has burning feet and has FMS.

That perifial(sp) neuropathology can be painful too, maybe that has similar symptoms. I think I have it on my scalp. It hurts and feels like a temporary bee sting that lasts a second but not burning. Who knows with this stuff. I just hope you feel better soon.

Hugs,

LMdimonds68 <Dimonds6881@...> wrote:

Hey there Cricket. How are you? I read your post about the burning skin. I have that also, although I have not had that in a few months. I do not have perepherial neropothy(sp?) . I have been tested for that. For me, it is just part of the Fibro flares. I know what you mean by it feels like the skin is on 'fire'. Sometimes the pain comes with the burning, but other times, the burning is just by itself. Strange, huh? I get the burning on my scalp too! I have read on other message boards/Fibro boards/ that other woman have this crazy symptom too. I am not sure what it can be except for what someone said in an earlier post that it can just be a flare up of some kind, and may come and go. Hopefully it just goes. Have you been detoxing. Ever scince I did those 2, 3day juice fasts with enemas, my health has turned around alot for the

better(and the warm wheather helps too!) I am planning to do another one next week. Now if I could just stop this hair loss, and the yeast problem, I can deal with the rest. Peace, hugs, and health to you always. TERRY

July 6, 2004

FMS and peripheral neuropathy can go hand in hand.

Lynda

At 11:39 PM 7/5/2004, you wrote:

>Hi Cricket:

>I think Terry is correct b/c I read about burning with FMS. Rogene has

>burning feet and has FMS.

>

>That perifial(sp) neuropathology can be painful too, maybe that has

>similar symptoms. I think I have it on my scalp. It hurts and feels like a

>temporary bee sting that lasts a second but not burning. Who knows with

>this stuff. I just hope you feel better soon.

>

>Hugs,

>LM

>

>dimonds68 <Dimonds6881@...> wrote:

>Hey there Cricket. How are you? I read your post about the burning