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Hi All-

I am glad to have found this group and hope to learn much about what is

happening to me by listening to what everyones opinion and personal stories.

One thing I am curious about is that how many have problems with lab work?

What I mean is, over the past two years I have had the exact symptoms of CP

( I had my gallbladder removes 3 years earlier) and my lab work that is done

the day after my pain shows High liver function levels, high cholestoral but

no high lipase or amylase levels. The doctor thinks I have CP but is not

sure. I also have an enlarged liver and spleen.

They are now looking at having me go to the ER and have blood work done as

soon as I start having the pain rather than later on or the next day.

Has anyone else experianced this? Is this common? Or do I not even have CP?

Its so frustrating!! Especially since I went through this with my

endometriosis (took 4 years). Endometriosis has been ruled out for this pain

and nausa.

Any advice or personal stories similar?

Thanks!!

Mecus

" MoonShadow "

jenmecus@... (private email)

jmecus3@... (family email)

MECUS@... (school email)

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