Guest guest Posted November 16, 2002 Report Share Posted November 16, 2002 Hey All, I am not able to read all of your posts to me but will when I have more time. Weston and did call me. If anyone else tried to call and hasn't gotten a hold of us, then we were probably pacing the halls. called right before she was to get some reglan, told me about her reactions to it and I told the nurse not to give Jackie anymore of it. The doc said she could have phenagran...don't know why now and not when she was first in there. Anyways, I was told her exact levels (lipase) yesterday...Tuesday at the ER they were 3400...then Wed morn they were up to 4736, Fri morn they were 1035 so the are going down. And she slept last night about 2 two hour periods and she is not pacing and walking as much. I do think she has a habit now of wanting to " go walking " but she has calmed down a good bit. I so appreciate 's call at the right time...she was fixing to have more of that junk. The nurse said she had never heard of that reaction, oh well. The nurse did start giving her 75 mg of dermerol and said she didn't know why she wasn't given the highest allowed dose, they told me it was 50. Then the night nurse goes back to 50 with phenagran...I think I will make them go to the 75 again today, just makes you mad you have to argue with them. She seems to be in the same amount of pain but am hoping the levels will continue to drop and she will be out of there soon. Got a call from the MUSC and her ERCP will be the day before Thanksgiving...I agreed cuz I am ready to see if this will be any help and if they can find something. I will read ya'lls posts when we get home from the hospital and I will write to you all when she is home. I am hoping only 2-3 more days. Thanks for all of your support, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 16, 2002 Report Share Posted November 16, 2002 teresa, I read both your posts. So glad Jackie's levels are going down. Ya know, I just don't get nurses and pain med. There were times my doc wrote the order for 25-50 mg demerol every 2 hours as needed. They never told me I could have 50 and only gave me 25 even during times I told them it didn't totally take care of the pain. Of course, I never knew the order said 25-50 and I really didn't know what they were giving me. I just knew that a few times I needed more before time and they told me I couldn't have it. When I read the chart, I saw the order was for 25-50 but they only gave me 25 every time I asked for it. They never charted the times I asked for it early, but I remember them. I never told the doctor cause by the time I saw him again, I was better and the 25 was taking care of the pain for long enough. I just don't get the lies. Glad they quit giving Jackie the reglan. I can't believe the nurse never heard of that reaction to reglan. Maybe they should all check one of the prescription drug sites for potential side effects! It was right there in black and white!!! (as I'm sure you saw in the e-mail I sent you - I read it word for word to you on the phone) Just goes to show, we must ALWAYS be aware of potential side effects of meds and pay attention to our bodies cause the nurses and doctors may not even know of some side effects! Boy, kind of scary when at times you are so sick and out of your mind with pain/nausea/vomiting when in their care! Take care and keep us informed on Jackie's progress. w Update on Jackie... Hey All, I am not able to read all of your posts to me but will when I have more time. Weston and did call me. If anyone else tried to call and hasn't gotten a hold of us, then we were probably pacing the halls. called right before she was to get some reglan, told me about her reactions to it and I told the nurse not to give Jackie anymore of it. The doc said she could have phenagran...don't know why now and not when she was first in there. Anyways, I was told her exact levels (lipase) yesterday...Tuesday at the ER they were 3400...then Wed morn they were up to 4736, Fri morn they were 1035 so the are going down. And she slept last night about 2 two hour periods and she is not pacing and walking as much. I do think she has a habit now of wanting to " go walking " but she has calmed down a good bit. I so appreciate 's call at the right time...she was fixing to have more of that junk. The nurse said she had never heard of that reaction, oh well. The nurse did start giving her 75 mg of dermerol and said she didn't know why she wasn't given the highest allowed dose, they told me it was 50. Then the night nurse goes back to 50 with phenagran...I think I will make them go to the 75 again today, just makes you mad you have to argue with them. She seems to be in the same amount of pain but am hoping the levels will continue to drop and she will be out of there soon. Got a call from the MUSC and her ERCP will be the day before Thanksgiving...I agreed cuz I am ready to see if this will be any help and if they can find something. I will read ya'lls posts when we get home from the hospital and I will write to you all when she is home. I am hoping only 2-3 more days. Thanks for all of your support, PANCREATITIS Association, Intl. Online e-mail group To reply to this message hit & quot;reply & quot; or send an e-mail to: Pancreatitis (AT) Yahoo Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 16, 2002 Report Share Posted November 16, 2002 teresa, I read both your posts. So glad Jackie's levels are going down. Ya know, I just don't get nurses and pain med. There were times my doc wrote the order for 25-50 mg demerol every 2 hours as needed. They never told me I could have 50 and only gave me 25 even during times I told them it didn't totally take care of the pain. Of course, I never knew the order said 25-50 and I really didn't know what they were giving me. I just knew that a few times I needed more before time and they told me I couldn't have it. When I read the chart, I saw the order was for 25-50 but they only gave me 25 every time I asked for it. They never charted the times I asked for it early, but I remember them. I never told the doctor cause by the time I saw him again, I was better and the 25 was taking care of the pain for long enough. I just don't get the lies. Glad they quit giving Jackie the reglan. I can't believe the nurse never heard of that reaction to reglan. Maybe they should all check one of the prescription drug sites for potential side effects! It was right there in black and white!!! (as I'm sure you saw in the e-mail I sent you - I read it word for word to you on the phone) Just goes to show, we must ALWAYS be aware of potential side effects of meds and pay attention to our bodies cause the nurses and doctors may not even know of some side effects! Boy, kind of scary when at times you are so sick and out of your mind with pain/nausea/vomiting when in their care! Take care and keep us informed on Jackie's progress. w Update on Jackie... Hey All, I am not able to read all of your posts to me but will when I have more time. Weston and did call me. If anyone else tried to call and hasn't gotten a hold of us, then we were probably pacing the halls. called right before she was to get some reglan, told me about her reactions to it and I told the nurse not to give Jackie anymore of it. The doc said she could have phenagran...don't know why now and not when she was first in there. Anyways, I was told her exact levels (lipase) yesterday...Tuesday at the ER they were 3400...then Wed morn they were up to 4736, Fri morn they were 1035 so the are going down. And she slept last night about 2 two hour periods and she is not pacing and walking as much. I do think she has a habit now of wanting to " go walking " but she has calmed down a good bit. I so appreciate 's call at the right time...she was fixing to have more of that junk. The nurse said she had never heard of that reaction, oh well. The nurse did start giving her 75 mg of dermerol and said she didn't know why she wasn't given the highest allowed dose, they told me it was 50. Then the night nurse goes back to 50 with phenagran...I think I will make them go to the 75 again today, just makes you mad you have to argue with them. She seems to be in the same amount of pain but am hoping the levels will continue to drop and she will be out of there soon. Got a call from the MUSC and her ERCP will be the day before Thanksgiving...I agreed cuz I am ready to see if this will be any help and if they can find something. I will read ya'lls posts when we get home from the hospital and I will write to you all when she is home. I am hoping only 2-3 more days. Thanks for all of your support, PANCREATITIS Association, Intl. Online e-mail group To reply to this message hit & quot;reply & quot; or send an e-mail to: Pancreatitis (AT) Yahoo Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 16, 2002 Report Share Posted November 16, 2002 teresa, I read both your posts. So glad Jackie's levels are going down. Ya know, I just don't get nurses and pain med. There were times my doc wrote the order for 25-50 mg demerol every 2 hours as needed. They never told me I could have 50 and only gave me 25 even during times I told them it didn't totally take care of the pain. Of course, I never knew the order said 25-50 and I really didn't know what they were giving me. I just knew that a few times I needed more before time and they told me I couldn't have it. When I read the chart, I saw the order was for 25-50 but they only gave me 25 every time I asked for it. They never charted the times I asked for it early, but I remember them. I never told the doctor cause by the time I saw him again, I was better and the 25 was taking care of the pain for long enough. I just don't get the lies. Glad they quit giving Jackie the reglan. I can't believe the nurse never heard of that reaction to reglan. Maybe they should all check one of the prescription drug sites for potential side effects! It was right there in black and white!!! (as I'm sure you saw in the e-mail I sent you - I read it word for word to you on the phone) Just goes to show, we must ALWAYS be aware of potential side effects of meds and pay attention to our bodies cause the nurses and doctors may not even know of some side effects! Boy, kind of scary when at times you are so sick and out of your mind with pain/nausea/vomiting when in their care! Take care and keep us informed on Jackie's progress. w Update on Jackie... Hey All, I am not able to read all of your posts to me but will when I have more time. Weston and did call me. If anyone else tried to call and hasn't gotten a hold of us, then we were probably pacing the halls. called right before she was to get some reglan, told me about her reactions to it and I told the nurse not to give Jackie anymore of it. The doc said she could have phenagran...don't know why now and not when she was first in there. Anyways, I was told her exact levels (lipase) yesterday...Tuesday at the ER they were 3400...then Wed morn they were up to 4736, Fri morn they were 1035 so the are going down. And she slept last night about 2 two hour periods and she is not pacing and walking as much. I do think she has a habit now of wanting to " go walking " but she has calmed down a good bit. I so appreciate 's call at the right time...she was fixing to have more of that junk. The nurse said she had never heard of that reaction, oh well. The nurse did start giving her 75 mg of dermerol and said she didn't know why she wasn't given the highest allowed dose, they told me it was 50. Then the night nurse goes back to 50 with phenagran...I think I will make them go to the 75 again today, just makes you mad you have to argue with them. She seems to be in the same amount of pain but am hoping the levels will continue to drop and she will be out of there soon. Got a call from the MUSC and her ERCP will be the day before Thanksgiving...I agreed cuz I am ready to see if this will be any help and if they can find something. I will read ya'lls posts when we get home from the hospital and I will write to you all when she is home. I am hoping only 2-3 more days. Thanks for all of your support, PANCREATITIS Association, Intl. Online e-mail group To reply to this message hit & quot;reply & quot; or send an e-mail to: Pancreatitis (AT) Yahoo Quote Link to comment Share on other sites More sharing options...
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