Re: Re: More ?'s!!...

[Guest guest]

Has anyone ever thought the pain could be coming from somewhere else, like

me and my new-found duendenal ulcer(located about 1 centimeter from my

gallbladder!)

>>

_____________

That's possible, too, . It may be coming from another source.

Susie

[Guest guest]

Has anyone ever thought the pain could be coming from somewhere else, like me

and my new-found duendenal ulcer(located about 1 centimeter from my

gallbladder!)

barry91162 <barry91162@...> wrote: ,

This is very easy to answer. Everyone's body is different. Why would

my one 1cm gb stone cause me to loose hours of sleep and your many

stones do not?

Why do some people live all their lives with a gb full of calcified

stones and never feel any pain? Bile consistancy? Some bile can flow

easier than others. You could have a 3cm calcified stone and never

feel pain as long as the bile can flow past it. Duct size at the

mouth, shape of the stone (oval, round). There can be many factors

for the difference. Just be glad yours haven't caused you severe

pain....yet. Getting them out is the only way to insure they will not

one day bother you more.

Good luck with your health.

Barry.

> barry91162@y...

> writes:

> > IMO, this type of stone is what most of us get colic

> > pain from. Sludge and such is discomforting but the pain of a

hard gb

> > stone blocking the mouth and stopping up the bile is terrible.

>

>

> Okay, I'll throw this into the mix. On the one hand, I've

seen my

> ultrasound films and it appears that there are several white spots

which we

> think would indicate calcified stones because the cholesterol ones

wouldn't

> show up, right? (correct me if I've misunderstood this.) On the

other

> hand, you think it's the calcified stones that cause the pain,

right?

>

> Then why do you suppose, if my ultrasound appears to be showing

calcium

> stones, am I not getting the colic pain that some of you describe?

I've had

> something similar, but much shorter in duration and definitely not

the

> frequency that others have written about. And trust me - I haven't

refined

> my dietary habits that well! In the past few months since the

attacks first

> happened, I've had some days of pretty unhealthy eating. (nothing

I'm proud

> of, but am just admitting it to give the whole picture)

>

> Any speculation? I'm not complaining - let me clarify! I'm

VERY grateful

> that I haven't had the experiences that some of you have written

about. I'm

> just puzzled by why mine ARE less severe when it would seem by the

ultrasound

> that I have calcified stones in there.

>

> I think I'm going to take those films to work with me on Monday and

just keep

> asking until I find someone in the health care departments who

might be able

> to tell me what they see.

>

> in health,

> rachel~

[Guest guest]

Susie,

The way I found out was this:

During my Hidoscan xray I put a lead object (that the Technologist gave me)

right over the area of pain. >>

________________

, I know that I have gallstones. I had an ultrasound Dec. of 2000 in

the ER, and after that is when I started doing cleanses.

Also when I first started having any kind of pain in this area, I was having

reflux. It took me some time to realize that it was my gallbladder. I'd say

about a year. One day I was having a reflux and it was just a wee little bit

different, then I decided it was my GB. When I had that horrible attack in

Dec. of 2000, I also had a reflux with it, which the doc said wasn't unusual

at all with GB attacks.

Now I'm fixing to be doing cleanse #13 or 14, I think. I've lost count. I'm

in the process right now. But since I found out it was my GB, I've changed

my diet, take vitamins, drink lots of water, and since the Beta-TCP, I've had

even less problems. Doesn't mean that I won't ever having any more problems

again, though. I look at it as a day-to-day journey.

Susie

[Guest guest]

< I really hope you get better soon!

>>

_______________

Thanks, . I appreciate the thought. BTW, I drank my first dose of ES

about 20 minutes ago. Gross!

Susie

[Guest guest]

Susie,

The way I found out was this:

During my Hidoscan xray I put a lead object (that the Technologist gave me)

right over the area of pain.

(I had to use such an object because since it's a " nuclear " machine it only

would pick up a lead object.)

When I asked the technologist what it was on she said it was an inch away from

the gallbladder on the duendenum(or small intestine!)

Sometimes you must " get smart " to figure out where the pains are coming from,

because my Docter's taking too long!

Good luck!

Tishri7@... wrote: Has anyone ever thought the pain could be coming from

somewhere else, like

me and my new-found duendenal ulcer(located about 1 centimeter from my

gallbladder!)

>>

_____________

That's possible, too, . It may be coming from another source.

Susie

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[Guest guest]

Susie,

I really hope you get better soon!

P.S. I've read that many people with gallstones are deficient in minerals and

electrolytes, especially organic sodium.

If you can drink lots of Carot/celery juice which is high in organic sodium!The

gallbladder needs these minerals to manufacture sufficient and healthy bile.

Tishri7@... wrote: Susie,

The way I found out was this:

During my Hidoscan xray I put a lead object (that the Technologist gave me)

right over the area of pain. >>

________________

, I know that I have gallstones. I had an ultrasound Dec. of 2000 in

the ER, and after that is when I started doing cleanses.

Also when I first started having any kind of pain in this area, I was having

reflux. It took me some time to realize that it was my gallbladder. I'd say

about a year. One day I was having a reflux and it was just a wee little bit

different, then I decided it was my GB. When I had that horrible attack in

Dec. of 2000, I also had a reflux with it, which the doc said wasn't unusual

at all with GB attacks.

Now I'm fixing to be doing cleanse #13 or 14, I think. I've lost count. I'm

in the process right now. But since I found out it was my GB, I've changed

my diet, take vitamins, drink lots of water, and since the Beta-TCP, I've had

even less problems. Doesn't mean that I won't ever having any more problems

again, though. I look at it as a day-to-day journey.

Susie