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,

Theresa 2 here. I also suffer from IBS and I was told exactly what

you said, by both my internist and gastroenterologist. I thought

that as many million people who suffer from this disease, to

determine you have it, by excluding all other " specific " diseases is

pretty insulting.

I have had times when it has driven me home, its been so horrible.

When I am nervous or stressed, it gets really, really bad. The only

medicine that finally stablized my condition, Lotremex, was recently

pulled off the market! I was devestated. I am hoping that the DS

will not exacerbate my IBS as did for Liane.

Hugs,

Theresa

(da udder one!)

>

> In a message dated 9/25/01 11:12:57 PM, duodenalswitch@y... writes:

>

> << Hate to burst your bubble, but IBS is not at all like

fibromyalgia..

>

> there are specific tests for diagnosis, and specific meds that work

to

>

> ease the symptoms. >>

>

> I've always heard that IBS was rather 'vague' to diagnose in many

cases as

> well. It is often diagnosed after other things are totally ruled

out. I'm

> sure there are tests which can help the diagnosis -- my spastic

colon

> happened to occur during the colonoscopy. However, I think that if

a

> colonoscopy turns up negative, the diagnosis of IBS is mainly based

on the

> negative presence of other diseases, not necessarily a positive

confirmation

> of the presence of IBS through testing. Can you tell me what other

tests

> there are? I was told that IBS was a general term used when

nothing else

> could be found by my gastroenterologist.

>

> I'm sure there are meds that work (they have even found that some

> anti-anxiety/anti-depressant drugs can work, perhaps by 'calming'

an

> overactive nervous system). I was given an anti-spasmodic in

particular for

> my colon. But, I know that others can have really vague symptoms

that are

> not as easy to diagnose except as a process of elimination.

>

> Now, IBD (Irritable Bowel Disease) is a collection of ailments that

ARE

> specifically easier to detect. I've read and heard that with IBS

there *may

> not* be a specific anatomical fact that points to the IBS and

therefore it is

> more difficult to pinpoint. This is especially true if it is

primarily

> neurological in nature as opposed to an abdominal defect or

condition that

> can be readily seen via testing. I think this may have been what

was

> mentioning in his response. There may be a lot more research done

on IBS

> that I am unaware of even though I have this condition but from

what I have

> researched there isn't a whole lot known about the causes and the

symptoms

> are wide and can be rather 'vague' and difficult to

diagnose/pinpoint. I

> believe that fibromalygia shares these qualities.

>

> all the best,

>

> lap ds with gallbladder removal

> January 25, 2001

> Dr. Gagner/Mt. Sinai/NYC

>

> eight months post-op and still feelin' fabu! :)

>

> preop: 307 lbs/bmi 45

> now: 215

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