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Hello, everyone. I just joined and thought I would let you know

something about me. I am 36yo wmf 1 child 10 years old, 2 steps.

The older 2 have moved out, so we are just raising our daughter.

Well, that's not totally true - the oldest daughter and her family is

living with us for a short time.

ANYWAY--I was only diagnosed last year, but I have had symptoms for

at least 12. This is so unknown! I have been tested for RA, Lupus,

Lyme's disease, and probably other things I don't remember off hand.

My breakthrough came last year when I read a magazine article about

FMS and thought " This is it. " I saw my dr and told him I thought it

was fibro, and he did the tender point test. Voila! a diagnosis!

Finally, a medical basis for my problems!

Although the pain is a daily companion, my worst problem with fms is

the fibro-fog. I used to work for a charity - which I wlll not name

due to fibro related problems that caused me to leave there - after

Sept. 11 we became so busy and stressed that my fibro kicked into

HIGH gear and my fog took over my mind. Looking back, I think that I

was on the verge of a nervous break down from trying to deny what was

going on. My boss accused me of using my fibro as an excuse not to

do my job (because I would forget things I was told, or lose track of

what I was doing.) If you do not have fibro-fog, I pray that you

miss out on this part of the disease. If you do have it, I would be

interested in learning new ways to cope.

I am going to stop here to check out the archives. anxiously await

future posts.

Kathy

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