Re: anyone mis-dxed with MS?

January 3, 2001

Pepi,

I am one who has been misdiagnosed with MS-of course the Dr's would

disagree with that statement but then I am from Texas where mostly all

Dr's are still denying Lyme disease is here. I have seen a number of Neuro

Dr's, Texas and Illinois and finally in 1998 was told probable MS-this

last one won't even discuss Lyme desease with me. I finally received my

blood lab report from Dr M's office and it sure looks like to me I have

Lyme disease and am treating with the Rife as Dr's have given me no choice

at all. I have herx's with that treatment, I have herx's with antibotics

but after treating myself for a couple of months I can begin to say I no

longer feel like I am dying everyday now like it used to be. I still have

alot of bad days but now they are mixed with a few days of being able to

feel like I am living. I had 3 MRI's, all the other tests for MS and only

came up with "probable MS" so as far as I am concerned it still isn't,

I have many more problems/symptoms of Lyme than I do MS problems.

Coleen

pepi wrote:

I would like anyone

that has been misdiagnosed with MS write a brief story about how, when,

why etc. I do research for an MS board and some of them are starting

to question their MS dx, especially with that Tom Grier article ( I posted

it on the MS board also ) Thanks so much, take care ,

Pepi

HAPPY NEW YEAR!!!

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January 4, 2001

Thank You Colleen, I forgotten that you had this dx. How have you been? Getting any relief yet? Let me know how you like that rife. Take care, Pepi

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