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Re: IBS

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If your current PCP refuses to even give you meds to be used " as

needed, " you can also use Immodium to combat some symptons.. but to

prevent the cramping, you'd need an anticholonergic drug. One common

one available over the counter is Dramamine.. but you need to tell

your current PCP that IBS can cause loss of control.. which is not

acceptable! There are quite a few medications available to treat IBS..

you just may have to push your doc to write the appropriate script.

Whatever happens.. take care, & let us know if you got through to him.

Hugs,

Liane

> Hello! This is an enbarassing problem but I have to ask.I have not

> had surgery as of yet.I do however have IBS which was diagnosed in

> 1996 one year after gullbladder removal.I am not on any medications

> as my current pcp feels that I can manage this with proper diet,ok

so

> im going to see a new pcp in november.What can i do imn the

meantime?

> Tara

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  • 2 weeks later...

Chris..

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. If it were a gluten allergy, I should never have

missed 3 weeks from work, or for that matter, had troubles prior to

trying to go back to work. I did not eat any bread or

gluten-containing products for the first 3 months of my surgery.. I

ate chicken, beef, and veggies. I'm happy that your friend resolved

his IBS-like symptoms by ruling out gluten products.. but it was not

dietary for me. I had gut spasms on broth and jello. I was on broth

and jello for most of a month. I think that could safely rule out milk

products and gluten. My troubles are not dietary.

Thanks for the input, though.

Hugs,

Liane

> > > What are the symptoms of irritable bowel syndrome? Is there an

> > > effective treatment?

> > >

> > > Ann

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And to further complicate the issue, IBS frequently is seen in

patients that have Fibromyalgia, along with Irritable Bladder,

migraine headaches, myofascial pain syndrome, arthritis, nerve

entrapment syndromes, neuralgia, restless legs syndrome, and many

others...

Just don't let anyone tell you that fibromyalgia isn't a " real "

illness-- as someone who has lived with this diabolical disease for

many, many years, I know just how real it is.

-- Joy Frost

> > > > What are the symptoms of irritable bowel syndrome? Is there an

> > > > effective treatment?

> > > >

> > > > Ann

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> And to further complicate the issue, IBS frequently is seen in

> patients that have Fibromyalgia, along with Irritable Bladder,

> migraine headaches, myofascial pain syndrome, arthritis, nerve

> entrapment syndromes, neuralgia, restless legs syndrome, and many

> others...

>

> Just don't let anyone tell you that fibromyalgia isn't a " real "

> illness-- as someone who has lived with this diabolical disease for

> many, many years, I know just how real it is.

>

Joy..

I do realize that fibromyalgia is real.. my mom has it, too. She also

has CFIDS, and I get tired of hearing that its not a " real " disease,

too. I'm sure my mom chooses to feel bad <sarcasm, in case no one

figues it out>.. just like she chooses to have muscle spasms so strong

that she'll " throw " things across the room.

Sometimes I wish that those who don't feel that newer diseases are

" real " would have to experience them some time.. might just open their

eyes, yanno? Because infection does not manifest itself in CFIDS

patients' labs the same as " normal " folk, my mom was told that the

infection in her elbow prosthesis didn't exist. But when they went in

to remove the prosthesis and check for infection.. it was so bad that

they closed immediately to prevent contamination the OR... the

[WARNING, GRAPHIC] pus was so old and thick it looked like peanut

butter. It was pretty obvious that there really had been a very

long-term infection in that joint.. despite her " normal " labs.

Sigh..

Liane

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,

Yup...on my birth certificate, my name is Theresa Marie, but on my

baptisimal certificate, its teresa maria....I guess, since I was the

youngest in a large Mexican Family, my sisters coerced my mom into

americanizing my name....but she held out on the religious stuff!

Laughing,

The other Theresa Marie

>

> In a message dated 9/26/01 1:11:23 PM, duodenalswitch@y... writes:

>

> << 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.

>

> >>

>

> Theresa: I know -- it is insulting that, so far as I know, there

really

> isn't any other clear cut way to diagnose this debilitating disease

or, in

> many instances, be unable to immediately and clearly help those who

suffer

> from it.

>

> I can only hope that they learn more about this disease (especially

it's

> origins in the nervous system) and be able to more appropriately

diagnose and

> treat it -- if not cure it!

>

> I suffer when under stress, too but I can say that my overall

condition has

> not been affected by the DS. It's actually been better. It is

really only

> when I'm stressed out that the symptoms re-appear. Now, I didn't

have

> diahhrea pre-op and don't really now (it is extremely rare for me

to have

> extremely loose bowels but it does happen on ocassion). I do get

spastic

> colon and/or various intestinal aches and pains, however. :)

>

> Hey - is your middle name Marie, too? I noticed that in your

screenname! :)

>

> 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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