Jump to content
RemedySpot.com

going home

Rate this topic


Guest guest

Recommended Posts

Hi Everyone,

Just wanted to let you know they are releasing me

today.

It would seem that this pain has nothing to do with my

pancreas...since my A & L are not elevated. I still

can't eat, still have diahrea (even though I have only

had ice chps allday) and still have dry heaves.

I am quite preturbed at this whole incident. If I'd

have thought this was something I could have dealt

with at home I would have stayed there.

I'm sure you have all heard this before from the docs

so you can't be too surprised. So for now I am

waiting for some clothes and my ride home. I hope

that this surgery really does take care of the pain

because if one more " Health care PROFESSIONAL " tells

me thi isn't CP... I'm going to pop them in the nose.

I should be hom by 6 pm EST. So I'll get to my

messages then, Thanks everyone for your concern and

prayer.

{{{HUGZ}}}

__________________________________________________

Link to comment
Share on other sites

Hi ,

I glad that they are sending you home, but it doesn't sound like your any better

off than when you went into the hospital. What are you suppose to do for

yourself when you get home since you not eating anything yet and are only on ice

chips. Since your enzymes aren't elevated & your supposedly don't have CP, what

do you have. I'm so sick and tired of these docs telling us that it not CP,

when we don't having elevated enzymes. We MUST really educate them somehow. I

wish I knew how. I go thru this same problem with our local ER docs here too.

They all give me a pain where I sit. I think once you do have a CP and you have

a flare-up, we know what it certainly feels like and we certainly know our

bodies better than these so called ER docs. They should really believe us. I

saw a new doc today( or should I say yesterday now) as it was on Wed. I ask him

about elevated enzymes with CP as it progress and his said that it's not at all

uncommon NOT to have them elevated as the disease progress. Maybe I should have

ask him for that in writing, so my ER doc would believe me. So much for my

preaching for today. I just wish you felt a whole lot better. Do take care and

try not do too much when get home. It sound like you still need to take it easy

for a while. Hopefully they gave you pain and nausea meds to take at home. Any

new word on your other surgery yet. Keep us posted, as I do care on how your

feeling. Hopefully for better days ahead on Thursday and over the Weekend.

Take Care,

Louie in WV

going home

Hi Everyone,

Just wanted to let you know they are releasing me

today.

It would seem that this pain has nothing to do with my

pancreas...since my A & L are not elevated. I still

can't eat, still have diahrea (even though I have only

had ice chps allday) and still have dry heaves.

I am quite preturbed at this whole incident. If I'd

have thought this was something I could have dealt

with at home I would have stayed there.

I'm sure you have all heard this before from the docs

so you can't be too surprised. So for now I am

waiting for some clothes and my ride home. I hope

that this surgery really does take care of the pain

because if one more " Health care PROFESSIONAL " tells

me thi isn't CP... I'm going to pop them in the nose.

I should be hom by 6 pm EST. So I'll get to my

messages then, Thanks everyone for your concern and

prayer.

{{{HUGZ}}}

__________________________________________________

Link to comment
Share on other sites

Hi ,

I glad that they are sending you home, but it doesn't sound like your any better

off than when you went into the hospital. What are you suppose to do for

yourself when you get home since you not eating anything yet and are only on ice

chips. Since your enzymes aren't elevated & your supposedly don't have CP, what

do you have. I'm so sick and tired of these docs telling us that it not CP,

when we don't having elevated enzymes. We MUST really educate them somehow. I

wish I knew how. I go thru this same problem with our local ER docs here too.

They all give me a pain where I sit. I think once you do have a CP and you have

a flare-up, we know what it certainly feels like and we certainly know our

bodies better than these so called ER docs. They should really believe us. I

saw a new doc today( or should I say yesterday now) as it was on Wed. I ask him

about elevated enzymes with CP as it progress and his said that it's not at all

uncommon NOT to have them elevated as the disease progress. Maybe I should have

ask him for that in writing, so my ER doc would believe me. So much for my

preaching for today. I just wish you felt a whole lot better. Do take care and

try not do too much when get home. It sound like you still need to take it easy

for a while. Hopefully they gave you pain and nausea meds to take at home. Any

new word on your other surgery yet. Keep us posted, as I do care on how your

feeling. Hopefully for better days ahead on Thursday and over the Weekend.

Take Care,

Louie in WV

going home

Hi Everyone,

Just wanted to let you know they are releasing me

today.

It would seem that this pain has nothing to do with my

pancreas...since my A & L are not elevated. I still

can't eat, still have diahrea (even though I have only

had ice chps allday) and still have dry heaves.

I am quite preturbed at this whole incident. If I'd

have thought this was something I could have dealt

with at home I would have stayed there.

I'm sure you have all heard this before from the docs

so you can't be too surprised. So for now I am

waiting for some clothes and my ride home. I hope

that this surgery really does take care of the pain

because if one more " Health care PROFESSIONAL " tells

me thi isn't CP... I'm going to pop them in the nose.

I should be hom by 6 pm EST. So I'll get to my

messages then, Thanks everyone for your concern and

prayer.

{{{HUGZ}}}

__________________________________________________

Link to comment
Share on other sites

Hi ,

I glad that they are sending you home, but it doesn't sound like your any better

off than when you went into the hospital. What are you suppose to do for

yourself when you get home since you not eating anything yet and are only on ice

chips. Since your enzymes aren't elevated & your supposedly don't have CP, what

do you have. I'm so sick and tired of these docs telling us that it not CP,

when we don't having elevated enzymes. We MUST really educate them somehow. I

wish I knew how. I go thru this same problem with our local ER docs here too.

They all give me a pain where I sit. I think once you do have a CP and you have

a flare-up, we know what it certainly feels like and we certainly know our

bodies better than these so called ER docs. They should really believe us. I

saw a new doc today( or should I say yesterday now) as it was on Wed. I ask him

about elevated enzymes with CP as it progress and his said that it's not at all

uncommon NOT to have them elevated as the disease progress. Maybe I should have

ask him for that in writing, so my ER doc would believe me. So much for my

preaching for today. I just wish you felt a whole lot better. Do take care and

try not do too much when get home. It sound like you still need to take it easy

for a while. Hopefully they gave you pain and nausea meds to take at home. Any

new word on your other surgery yet. Keep us posted, as I do care on how your

feeling. Hopefully for better days ahead on Thursday and over the Weekend.

Take Care,

Louie in WV

going home

Hi Everyone,

Just wanted to let you know they are releasing me

today.

It would seem that this pain has nothing to do with my

pancreas...since my A & L are not elevated. I still

can't eat, still have diahrea (even though I have only

had ice chps allday) and still have dry heaves.

I am quite preturbed at this whole incident. If I'd

have thought this was something I could have dealt

with at home I would have stayed there.

I'm sure you have all heard this before from the docs

so you can't be too surprised. So for now I am

waiting for some clothes and my ride home. I hope

that this surgery really does take care of the pain

because if one more " Health care PROFESSIONAL " tells

me thi isn't CP... I'm going to pop them in the nose.

I should be hom by 6 pm EST. So I'll get to my

messages then, Thanks everyone for your concern and

prayer.

{{{HUGZ}}}

__________________________________________________

Link to comment
Share on other sites

Hi ,

I don't think my last message when thru to you, or at least that what my server

said, so just a quick note to let you know that I glad that you are home, but I

do wish you felt a whole lot better. I hope that they certainly sent you home

with nausea and pain meds, since they really didn't do much else to help you. I

sure you felt like that was a wasted trip to the hospital. I have felt that way

my last 2 trip that I was admitted for CP.

I do hope that you feel better Thursday and over the weekend. I'll keep you in

my prayers that your feeling better very soon. Keep us posted on how your

doing. Your always there for all of us, so let us be there for you now. Take it

easy and don't over do it now that you home. Be sure and rest as much as you

possible can.

Take Care,

Louie in WV

going home

Hi Everyone,

Just wanted to let you know they are releasing me

today.

It would seem that this pain has nothing to do with my

pancreas...since my A & L are not elevated. I still

can't eat, still have diahrea (even though I have only

had ice chps allday) and still have dry heaves.

I am quite preturbed at this whole incident. If I'd

have thought this was something I could have dealt

with at home I would have stayed there.

I'm sure you have all heard this before from the docs

so you can't be too surprised. So for now I am

waiting for some clothes and my ride home. I hope

that this surgery really does take care of the pain

because if one more " Health care PROFESSIONAL " tells

me thi isn't CP... I'm going to pop them in the nose.

I should be hom by 6 pm EST. So I'll get to my

messages then, Thanks everyone for your concern and

prayer.

{{{HUGZ}}}

__________________________________________________

Link to comment
Share on other sites

,

I'm just reading your post as I've been in the hospital myself. I, too, was

sick to death of the GI telling me that the pancreas wasn't cuaing the pain

since I had pain without the amylase and lipase being elevated. It took getting

my surgeon (the one who did my gastric bypass) involved to get the GI to admit

it most likely is the pancreas. Actually, they think it is the sphincter of

oddi malfunctioning which is causing the pain. According to my surgeon, there

are basically three levels of malfunctioning when it comes to the sphincter of

oddi.

1. The sphincter of oddi malfunctions for a short time anc causes episodes of

intense pain.

2. The sphincter of oddi malfunctions worse and causes liver enzyme elevations

in addition to the intense pain.

3. The sphinter of oddi really malfunctions and it causes enough irritation to

the pancreas that the pancreas enzyme levels (in addition to the liver enzyme

levels) are elevated.

My surgeon says that the pain is very real even when the enzymes are not

elevated. He also said that when your liver enzymes are very elevated your

liver is being damaged and something must be done to stop (or at least decrease)

the episodes.

going home

Hi Everyone,

Just wanted to let you know they are releasing me

today.

It would seem that this pain has nothing to do with my

pancreas...since my A & L are not elevated. I still

can't eat, still have diahrea (even though I have only

had ice chps allday) and still have dry heaves.

I am quite preturbed at this whole incident. If I'd

have thought this was something I could have dealt

with at home I would have stayed there.

I'm sure you have all heard this before from the docs

so you can't be too surprised. So for now I am

waiting for some clothes and my ride home. I hope

that this surgery really does take care of the pain

because if one more " Health care PROFESSIONAL " tells

me thi isn't CP... I'm going to pop them in the nose.

I should be hom by 6 pm EST. So I'll get to my

messages then, Thanks everyone for your concern and

prayer.

{{{HUGZ}}}

__________________________________________________

Link to comment
Share on other sites

,

I'm just reading your post as I've been in the hospital myself. I, too, was

sick to death of the GI telling me that the pancreas wasn't cuaing the pain

since I had pain without the amylase and lipase being elevated. It took getting

my surgeon (the one who did my gastric bypass) involved to get the GI to admit

it most likely is the pancreas. Actually, they think it is the sphincter of

oddi malfunctioning which is causing the pain. According to my surgeon, there

are basically three levels of malfunctioning when it comes to the sphincter of

oddi.

1. The sphincter of oddi malfunctions for a short time anc causes episodes of

intense pain.

2. The sphincter of oddi malfunctions worse and causes liver enzyme elevations

in addition to the intense pain.

3. The sphinter of oddi really malfunctions and it causes enough irritation to

the pancreas that the pancreas enzyme levels (in addition to the liver enzyme

levels) are elevated.

My surgeon says that the pain is very real even when the enzymes are not

elevated. He also said that when your liver enzymes are very elevated your

liver is being damaged and something must be done to stop (or at least decrease)

the episodes.

going home

Hi Everyone,

Just wanted to let you know they are releasing me

today.

It would seem that this pain has nothing to do with my

pancreas...since my A & L are not elevated. I still

can't eat, still have diahrea (even though I have only

had ice chps allday) and still have dry heaves.

I am quite preturbed at this whole incident. If I'd

have thought this was something I could have dealt

with at home I would have stayed there.

I'm sure you have all heard this before from the docs

so you can't be too surprised. So for now I am

waiting for some clothes and my ride home. I hope

that this surgery really does take care of the pain

because if one more " Health care PROFESSIONAL " tells

me thi isn't CP... I'm going to pop them in the nose.

I should be hom by 6 pm EST. So I'll get to my

messages then, Thanks everyone for your concern and

prayer.

{{{HUGZ}}}

__________________________________________________

Link to comment
Share on other sites

,

I'm sorry you were in that dreaded place too, I am glad though that your surgeon

was a help to you to open your GI's Eyes. I'd like to dot the doc I had in the

hosps eye!

Oh well, maybe my surgeon (when I get to go see him on the 20th will shed some

light onto this to my pcp.) Maybe.

I'm glad you are home and I hope things are going well (better) for you.

{{{HUGZ}}}

---------------------------------

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...