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Hi Friends:

Yesterday I posted a message that I was going to a new pain specialist today,

and was really having alot of anxiety about it. I could barely sleep, I kept

waking up with a start...mainly because I only had pain medication to last me

today, and no guarantee that the new doctor would even write me any

prescriptions at all.

Well, of course things never turn out as bad as I think they will be ... he was

a very nice doctor, and in fact thought it was very unprofessional for my pcp to

only give me enough medication to get to the new doctor. Since I am on

oxycontin, it's not something you should just stop taking. He mentioned that it

was lucky that he wasn't in a bad mood, or the type of doctor who wouldn't write

narcotic prescriptions right off the bat. I'm pretty grateful about that too.

Another thing he said was when he asked me what I thought started all the pain,

and I went back 4 years with my first attack, that the fact that in March they

did exploratory surgery (laproscopic) and only found a ruptured ovarian cyst and

fluid. Then in May when I had my next attack, they discovered my gall bladder

was full of sludge and stone. So, in one month's time I developed chronic

cholengetis? First doctor to actually admit this out loud. And then he went on

to say, another 1 1/2 years before they considered it might be something to do

with my pancreas??? He felt that there was enough education out there that it

should be fairly standard after removing the gall bladder, if pain returns to

take a look at the gall bladder. Anyhoooo...I digress...

What he did was increase my duragesic patch from 25 to 75, but didn't give me

any more oxycontin, of which I was taking 200 mg a day. Any thoughts on whether

anyone has followed a similar pain management pattern? He said I shouldn't go

through any type of withdrawal, because he replaced the oxy with enough of the

patch. I just took my last oxy...

Thanks everyone for your support and kind words...Hugs to all of you!

Robin

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