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Hello, Everyone.

Just got back from the GI specialist who advised me that

he feels that I do not have cp regardless of all my symptoms including the

pseudo cysts and the fact that I still need to use enzymes to help with my

digestion. He feels I have ibs. Strange though I have tried every option for

pain relief for those with ibs and nothing has worked yet. I know my pains are

coming from the pancreas however because the numbers don't show it the GI

refuses to do any further investigation. He is sending me to a neurologist with

the hopes of a nerve block for the pain management. Has anyone had one done? do

they work? what are the side effects? pros/cons? any advice would be great so

that I am good and informed for my meeting with the neurologist on December

2/05. Thanks............................

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,

I'm sorry I don't remember, but have you had an ERCP to confirm CP? Thats

conclusive evidense right there. I can't help you with the nerve block as as I

haven't had any?

Sandy in Ca

-------------- Original message --------------

Hello, Everyone.

Just got back from the GI specialist who advised me that

he feels that I do not have cp regardless of all my symptoms including the

pseudo cysts and the fact that I still need to use enzymes to help with my

digestion. He feels I have ibs.

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Do I understand correctly? Even the fact that you have pseudocysts does not

convince the man that you have pancreatitis? Is this guy some sort of

retard? Does he live on this planet? You had better run, and I mean run, to

another doc and never see this person again. And forget about the nerve

block until you can find a physician who diagnose you correctly.

Jerry/NC

*******************************************

>

> Hello, Everyone.

>

> Just got back from the GI specialist who advised me that he feels that I

> do not have cp regardless of all my symptoms including the pseudo cysts and

> the fact that I still need to use enzymes to help with my digestion. He

> feels I have ibs. Strange though I have tried every option for pain relief

> for those with ibs and nothing has worked yet. I know my pains are coming

> from the pancreas however because the numbers don't show it the GI refuses

> to do any further investigation. He is sending me to a neurologist with the

> hopes of a nerve block for the pain management. Has anyone had one done? do

> they work? what are the side effects? pros/cons? any advice would be great

> so that I am good and informed for my meeting with the neurologist on

> December 2/05. Thanks............................

>

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Sandy,

Had an ercp for the bile tract and sphincterotomy, however never was diagnoised

with cp. Had very serious acute post ercp pancreatitis which resulted in 3 cysts

that have never gone away and weeks in the hospital. The doctor did not preform

an ercp of the pancreas.

in Toronto, Ont., Canada

Re: nerve blocks

,

I'm sorry I don't remember, but have you had an ERCP to confirm CP? Thats

conclusive evidense right there. I can't help you with the nerve block as as I

haven't had any?

Sandy in Ca

-------------- Original message --------------

Hello, Everyone.

Just got back from the GI specialist who advised me

that he feels that I do not have cp regardless of all my symptoms including the

pseudo cysts and the fact that I still need to use enzymes to help with my

digestion. He feels I have ibs.

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