Guest guest Posted October 20, 2005 Report Share Posted October 20, 2005 Sorry, I am just so angry right now that I could tear a tree apart. just got back from his appointment at U of M with his regular GI doctor. She is a fellow. Every month she sees him, leaves the room to consult with the attending and then returns with the plan for the month. Today, the attending (one he has never seen before) came back in the room with her and said I don't t hink you have chronic pancreatitis. and Cheri are like " What are you talking about?? " She says after looking at his reports, she thinks there is an 80% chance that he does not have CP. Now what the heck does she think she is doing???? She says she wants to do an ERCP, but they were both so angry that she left saying she didn't want to do a procedure on someone who was so angry. He is so confused. Why would they treat him for over a year and then out of the blue, in comes a new doctor (who the fellow says is the " best " pancreas doctor there) decide to tell him he doesn't have pancreatitis. What the h... is wrong with him then???? It would be wonderful if he doesn't have it, but how can this team of doctors be so stupid. I am so mad, mad, mad. Who is the safest ERCP doctor you know about. Thanks LInda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 20, 2005 Report Share Posted October 20, 2005 I had the same problem with a new PCP (primary care phsycian....a step above an RB) and what the guy told me was that even though I have had CP for 19 yrs. That when he went through the schooling they only studied the pancreas and CP for two days. The way to take care of CP now a days is to prescribe some stomach enzymes and some pepcid. I looked right at the dude and rather then rip his head off I explained to him that since I have been on pain pills for such a long time that there would be no way that pepcid and stomach enzymes would help with pain relief. In the end the guy now refuses to take any patients that don't want pain pills. I told him that a disease like CP should be taught more then two days in a classroom. I even found out that some professor's don't talk about CP in class and they leave it up to the students to read about and understand it. I think that is why it is so hard for us to prove to ppl that we are sick cause there isn't enough stuff out there to try to explain what is going on. My best friend's sister developed CP while she was pregnant and then after a few months she got over it. I really belive that she never had CP but some type of stomach ailment. I haven't had an ERCP done since I was 15 because afterwards I ended up spening two weeks at vandy. My doc now want's me to have one done but my heart rate is out the roof (due to my thyroid dying) and my kidney's are failing. So if I don't respond too quickly...I am in the hospital....hope that everyone has had a pain free week... > > Sorry, I am just so angry right now that I could tear a tree apart. > just got back from his appointment at U of M with his regular GI > doctor. She is a fellow. Every month she sees him, leaves the room > to consult with the attending and then returns with the plan for the > month. Today, the attending (one he has never seen before) came back > in the room with her and said I don't t hink you have chronic > pancreatitis. and Cheri are like " What are you talking > about?? " She says after looking at his reports, she thinks there is an > 80% chance that he does not have CP. Now what the heck does she > think she is doing???? She says she wants to do an ERCP, but they > were both so angry that she left saying she didn't want to do a > procedure on someone who was so angry. He is so confused. Why > would they treat him for over a year and then out of the blue, in > comes a new doctor (who the fellow says is the " best " pancreas doctor > there) decide to tell him he doesn't have pancreatitis. What the > h... is wrong with him then???? It would be wonderful if he doesn't > have it, but how can this team of doctors be so stupid. I am so mad, > mad, mad. Who is the safest ERCP doctor you know about. Thanks LInda > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 20, 2005 Report Share Posted October 20, 2005 My best friend's sister developed CP while she was > pregnant and then after a few months she got over it. I really > belive that she never had CP but some type of stomach ailment. Keba, It highly likely was Pancreatitis. When I fell pregnant was when my attacks started all over again after a 15 month break. Although mine were not exactly related to the pregnancy, my OB/GYN told me it is not uncommon for pregnant women to suffer from Pancreatitis during their pregnancies only because to accomodate a baby, their insides are all pushed upwards and this can cause attacks of Panc to happen. Once the baby is born and everything has moved down back to where it should be, the pressure is gone and so do the attacks subside.. Regards, Ward PAI Administration Support dceward@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 28, 2005 Report Share Posted October 28, 2005 , Totally ridiculous deduction if you ask me, and one that I, personally, would pay no heed to. The best and safest doctors I know of to do an ERCP are Dr. Cotton at the Medical University of South Carolina, ton, SC or Dr. Lehman at Indiana University Medical Center, Indianapolis, Indiana. If you need more information about either one, please email me personally at: hhessgriffeth@... With love, hope and prayers, Heidi Heidi H. Griffeth Bluffton, SC SC State & SE Regional Representative Pancreatitis Association, International Note: All comments or advice are based on personal experience or opinion only, and should not be substituted for professional medical consultation. Quote Link to comment Share on other sites More sharing options...
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