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Re: Update on me

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Hi Alison,

The jaundice and pancreatitis are definite signs of obstruction. This

obstruction does not have to be stones. It can be inflammation infection etc.

They will still want to cut no matter what. Unfortunately since they changed

the format I can no longer insert into the message so I will try and answer up

here.

While low fat is a great idea to limit your chances of stimulating an

attack, it is like turning the water off and then trying to flush the toilet.

we need to keep the flow going to keep things from settling out and moving.

Quite the quandary. Emulsify, thin, flow and flush.

1 not necessarily. His concern is a valid one but not a sure thing.

2 possibly but not for sure. If they do one and they show up they are seen, if

they do not show up it does not mean something is not there. Most likely not

very big or dense though.

3 possible but doubtful.

4.This is one of those turning points where leaps of " faith " are an option. You

do not mention having attempted a flush since Nov. If not, this is precisely

the kind of situation where many people have had dramatic results. You can

always do one close to medical attention if you feel more comfortable. There is

no better source of information that I know of than the archives of this group.

Many such as Dale, Will , Vince and the like have suggestions on particular

books and protocols. Depending on diet , lifestyle and present physiologic

condition, changes in the above may be imperative. Even without performing a

flush or possibly beforehand in preparation, thinning, dissolving, stimulating.

As many point out there may be a parasitic component.

5 check out Dr. Mercola's stuff on diet.

www.mercola.com<http://www.mercola.com/>

----- Original Message -----

From: Alison Orr<mailto:alison@...>

gallstones <mailto:gallstones >

Sent: Monday, October 09, 2006 2:50 PM

Subject: Update on me

I posted a while ago about the two gallbladder attacks I'd had which put me

in hospital. The first time, in April, I had mild pancreatitis. The second

time, in June, I had jaundice and was very unwell. I've had 6 attacks

altogether between November 2005 and June 2006. I live in a rural area and

there's only a small cottage hospital nearby with a visiting surgeon. He

referred me for an MRCP but I freaked out in the MRI machine (I now know I

definitely *am* claustrophobic!). Since June, I've been following a very

low fat diet though recently I've begun to reintroduce (risk, more like!)

more fat into my diet. I've not had any attacks since June.

I've just heard from the surgeon and he wants to refer me for a " telescopic

examination of the bile duct... and I suspect there may be one or two stones

in this which have caused your recent jaundice and pancreatitis. "

I have a few questions:

1 Isn't it most likely that I'd have had another attack if I have stones in

my bile duct and have been eating more fat recently?

2 Could these stones not be detected with an ultrasound?

3 I had an ultrasound in April and only gravel and sludge were seen then.

Is it likely that I could have developed stones since then?

4 I don't want to let go of my gallbladder if I don't have to but I'm a bit

scared to do the flushes, especially if there are stones in the duct as I

could end up very ill again (or worse). I'm convinced flushes are a good

idea but what else should I be doing to improve my liver / gallbladder

health? Can you all (Dave Shelden please!) recommend websites and /or books

whose protocol I could follow? I would prefer to be able to compare several

rather than just blindly follow one.

6 I would like to try a GL (glycemic load) diet as I know I'm not eating

well at the moment. Anyone got thoughts on this?

Thanks in advance!

Alison

God bless

Give food to the hungry every day with a simple click, at no cost to you.

Visit http://www.thehungersite.com<http://www.thehungersite.com/> today!

--

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Checked by AVG Free Edition.

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  • 2 years later...

Hey Skip,

You'll be in our prayers. There's got to be one more drug out there

for you to try.

Hugs,

Vicki

>

> Hello all once again,

> just an update on my ongoing battle with my CML and the drugs to

combat it.

> After my last hospital stay, I was told not to use dasatinib any

more.

> They had to tap me and remove all the pleural infusion build up

caused by dasatinib.

> They removed 8.5 500ML bottles of liquid,over a threee week

period. After another 3 weeks my doc told me we would go back to

Nilotinib, at a reduced rate (400MG once day). In six days to the

hour, my liver enzymes shot through the roof. Once again I am off

any of the nibs, Imatinib, Nilotinib and Dasatinib. I am still a

bit sick and pain in the back but it is less that yesterday, so I

imagine I will wait until my doc comes back from ASH to find out

where we go from here. I am beginning to wonder if there is any of

these drugs I can tolerate. I guess I am paying the piper for

living so long with CML.

> Have a great day all

>

> SkipD

> dx'ed 30++++ years ago.

>

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Skip:

Don't give up the fight.? There are other medications,

other trials, even older drugs to use to fight.? We are

standing behind you so ask for help and you will get

it.

We believe in you my friend.

Matt M.

CML Motivation Department

Florida

[ ] Re: update on me

Hey Skip,

You'll be in our prayers. There's got to be one more drug out there

for you to try.

Hugs,

Vicki

>

> Hello all once again,

> just an update on my ongoing battle with my CML and the drugs to

combat it.

> After my last hospital stay, I was told not to use dasatinib any

more.

> They had to tap me and remove all the pleural infusion build up

caused by dasatinib.

> They removed 8.5 500ML bottles of liquid,over a threee week

period. After another 3 weeks my doc told me we would go back to

Nilotinib, at a reduced rate (400MG once day). In six days to the

hour, my liver enzymes shot through the roof. Once again I am off

any of the nibs, Imatinib, Nilotinib and Dasatinib. I am still a

bit sick and pain in the back but it is less that yesterday, so I

imagine I will wait until my doc comes back from ASH to find out

where we go from here. I am beginning to wonder if there is any of

these drugs I can tolerate. I guess I am paying the piper for

living so long with CML.

> Have a great day all

>

> SkipD

> dx'ed 30++++ years ago.

>

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>

> Hello all once again,

> just an update on my ongoing battle with my CML and the drugs to

combat it.

> After my last hospital stay, I was told not to use dasatinib any

more.

> They had to tap me and remove all the pleural infusion build up

caused by dasatinib.

> They removed 8.5 500ML bottles of liquid,over a threee week

period. After another 3 weeks my doc told me we would go back to

Nilotinib, at a reduced rate (400MG once day). In six days to the

hour, my liver enzymes shot through the roof. Once again I am off

any of the nibs, Imatinib, Nilotinib and Dasatinib. I am still a bit

sick and pain in the back but it is less that yesterday, so I imagine

I will wait until my doc comes back from ASH to find out where we go

from here. I am beginning to wonder if there is any of these drugs I

can tolerate. I guess I am paying the piper for living so long with

CML.

> Have a great day all

>

> SkipD

> dx'ed 30++++ years ago.

>

HI SKIP: You are a real trooper, and a great inspiration to all

of us. I will pray that they come up with a new method of treatment

for you. When Gleevec went into clinical trial, I had nothing going

for me. It was a sit and wait situation for me for months, just

using Hydrea. The trial came just in time for me, and I believe

something new will pop up soon. Just have faith and believe it will

all get better.

Suzzie

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