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Hi all,

I feel like I am going to explode lately. My last to visits to the

ER with pain have shown my amylase and lipase to both be normal, and

both times I've been sent home saying that everything is fine. I

don't have decent pain medicine to cope with the pain at home, my

doctor still hasn't returned my call and am still having an attack

after 24 hours...It really is infuriating..not to mention that the

doctors in the ER probably think I'm just there for a narcotic fix..

arghhhhhhhhhhhh...gets me so mad all I want to do is cry

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> Hi all,

>

> I feel like I am going to explode lately. My last to visits to the

> ER with pain have shown my amylase and lipase to both be normal,

and

> both times I've been sent home saying that everything is fine. I

> don't have decent pain medicine to cope with the pain at home, my

> doctor still hasn't returned my call and am still having an attack

> after 24 hours...It really is infuriating..not to mention that the

> doctors in the ER probably think I'm just there for a narcotic fix..

> arghhhhhhhhhhhh...gets me so mad all I want to do is cry

>

>

, I know your pain as, I would imagine, 99% of us in the

group. We have all been there at one point or another. Hang in

there. Don't let the insensitivity of these " professionals " deter

you from seeking remedies for your pain. I too never had an elevated

Amalase or lypase and this was a major cause for concern by many of

my " former " doctors. It has been my experience that doctors, when

confronted with something unfamiliar to them, will tend to dismiss

those things that don't fit the " textbook " answers. They are too

quick to label someone a " drug seeker " rather than trying to get at

the root cause of your discomfort. Don't let these insensitive oafs

make your life any worse than it is already. And alays remember, you

are not alone. We in this group all have experienced something

similar in our lives and had to get past this stage in order to

finally get the treatment needed. Have you tried a teaching

hospital? That's where I finally got a proper diagnosis and started

on my path to recovery. Just a thought...

Andre'

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Guest guest

> > Hi all,

> >

> > I feel like I am going to explode lately. My last to visits to

the

> > ER with pain have shown my amylase and lipase to both be normal,

> and

> > both times I've been sent home saying that everything is fine. I

> > don't have decent pain medicine to cope with the pain at home, my

> > doctor still hasn't returned my call and am still having an

attack

> > after 24 hours...It really is infuriating..not to mention that

the

> > doctors in the ER probably think I'm just there for a narcotic

fix..

> > arghhhhhhhhhhhh...gets me so mad all I want to do is cry

> >

> >

>

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Excellent suggestion, Andre'! My husband has necrotizing

pancreatitis due to an ERCP (what a nightmare). Anyway, his amylase

levels never elevated either. He spent two months in a local

hospital - they did what they could but no one

(doctors/nurses/technicians) never dealt with a case like Barry's.

Since he wasn't getting better, we got him to Pittsburgh to a

teaching hospital. It was relief when the nurse answered my

question with: " Yes, we see this (Barry's condition) fairly often. "

You need good, experienced treatment and a positive focus. Don't

cry, (unless it makes you feel better ... maybe a good ole

scream now and then too) .... take action! Get yourself feeling

better!

Beth

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