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Lurker - coming out!

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Hi

I've been lurking (in a nice way!) since the early days when you were

still the Marshall

Protocol group. I really appreciate this group still being here. I

never tried the MP, but

have following your experiences with interest. I was treated for acne

with Minocin, for

about 10 years on and off, through out the time when I was most ill

with M.E (CFS).

I've been ill since 1988. My acne reflects my immune system, it

really flares up during

relapses, boils and all (aagh!). Anyway I eventually stopped the

Minocin for fear of

what it was doing to my body, I'm not sure how it has effected my

M.E. One negative

side effect was that it caused staining of my front teeth.

I'm now using alternative health methods, diet, supplements, herbs

etc.. to battle

against the M.E, I managed to get myself to a manageable stage about

four years ago

and started a small business working from home. Unfortunately this

proved more

physically exhausting than I imagined, and I experienced a major

relapse around

Xmas 2003. This time around it seems to have effected my cognitive

functions

badly, I seriously considered that I might have a variety of

neurological problems,

Alzheimer's etc.. Which is why I've taken so long to post. I am still

very weak but

beginning to get my brain back a little.

Thanks to everyone for carrying on with the group despite all

adversities!

Jo in sunny England (well OK it rained a little today but spring is

definitely in the air!)

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