Amylase & Lipase elevated in Urine

[Guest guest]

Hi all,

This is Louie. I'm sorry that I haven't posted in a while. I have been feeling

better since July and have been doing other things and not on the internet very

much. I have been trying to read your post, even through I have been posting.

I have been thinking of you all and have certainly keep you all in my prayers.

In July , I changed to a new PCP after the urging from my daughters and spending

31 days in and out of the hospital from May 9th to July 1st. My old Pcp just

admitted me to the hospital and kind of let it run it course without trying to

find out why I had 3 very bad spell so close together. Well, the first time I

saw this new doc, I told him that my amlase and lipase were never elevated in my

blood test. Well, he said that made sense since all I have been thru. I was

impressed that I found someone who believed in me. He did say something rather

interesting-- He said that all lot of the time when someone is having a

flare-up, that The elevation of amylase and lipase will show up in the urine.

So he did a urine test and nothing show up at that time. This was after I was

out of the hospital and feeling better. I was wondering if anyone else doc, has

mention anything about the amylase and lipase being elevated in your urine. He

also switched my pain pill to MS Contin, 1 pill twice a day. He put me on the

long acting ones. Just last week , he gave me some short term ms-ir for

breakthrough pain, for when it rears its ugly head. They do seem to be helping

all lot. Well, that all folks. And I hope this finds you having a good

evening.

Take care, My Friends,

Louie in WV

[Guest guest]

Hi all,

This is Louie. I'm sorry that I haven't posted in a while. I have been feeling

better since July and have been doing other things and not on the internet very

much. I have been trying to read your post, even through I have been posting.

I have been thinking of you all and have certainly keep you all in my prayers.

In July , I changed to a new PCP after the urging from my daughters and spending

31 days in and out of the hospital from May 9th to July 1st. My old Pcp just

admitted me to the hospital and kind of let it run it course without trying to

find out why I had 3 very bad spell so close together. Well, the first time I

saw this new doc, I told him that my amlase and lipase were never elevated in my

blood test. Well, he said that made sense since all I have been thru. I was

impressed that I found someone who believed in me. He did say something rather

interesting-- He said that all lot of the time when someone is having a

flare-up, that The elevation of amylase and lipase will show up in the urine.

So he did a urine test and nothing show up at that time. This was after I was

out of the hospital and feeling better. I was wondering if anyone else doc, has

mention anything about the amylase and lipase being elevated in your urine. He

also switched my pain pill to MS Contin, 1 pill twice a day. He put me on the

long acting ones. Just last week , he gave me some short term ms-ir for

breakthrough pain, for when it rears its ugly head. They do seem to be helping

all lot. Well, that all folks. And I hope this finds you having a good

evening.

Take care, My Friends,

Louie in WV