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I have been sick for around 4 years. They had tried many different

things to help me and the pancrease enzymes have worked like a miracle

for the most part. Since I started on them I have had only 2 real bad

flare ups but the problem is that now when I have a flare up my doctor

believes that its caused by withdrawal from the iv meds and his nurse

pretty much blows me off when I call. He pretty much said that I'm

just imagining the pain. I just wondered if anyone else has gone

through this with their doctors. Thanks

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wrote:...

> He pretty much said that I'm

> just imagining the pain. I just wondered if anyone else has gone

> through this with their doctors.

,

This sounds too, too familiar. If only it were possible for these people

to experience a sample of what we go through. Just 5 minutes would

convince them. I am regularly reduced to tears trying to explain that I

need help with my pain. The doctor looks serious, sucks air through his

teeth, tut tuts, and gives me a lecture.

> my doctor

> believes that its caused by withdrawal from the iv meds and his nurse

> pretty much blows me off when I call.

If only these " experts " would read the literature they'd see that

withdrawal is not typical when people are taking opiate meds for PAIN

rather than for PLEASURE. In the past I was threatened with being

struck off my GP practice list ( " we don't treat junkies here " ) and

referred to the local addiction service psychiatrist because I was

taking 30mg MST am and pm. The psychiatrist didn't think I was an

addict. I felt humiliated.

Unfortunately these experiences of disrespect have left me feeling very

bitter - and very defensive. If someone vaguely implies that I might be

getting dependent on my meds I immediately react quite strongly -

thereby convincing them that they may have discovered that I really am

dependent.

However, last year I had a good phase and came off my pain meds (no need

to cut down I just stopped - I knew the literature and was confident).

But painless/ good phase came to an end and after 6 months my pain is

now worse than ever and the level of medication is inadequate. If things

continue along their present course, I'll soon need to seek permission

to increase my pain control again. I honestly do not want to have to sit

through another lecture.

Has anyone on the list found a way to cope with such idiots?

Rosie

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,

I think it's probably time to get another doctor if this one doesn't

believe that you are having flares. It is possible to have flares and

actual acute episodes with chronic pancreatitis while taking enzymes. If

your doctor doesn't know this, he's the wrong type of doctor to treat you.

Kimber

--

Kimber

Vallejo, CA

hominid2@...

Note: All advice given is personal opinion, not equal to that of a licensed

physician or health care professional.

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