Guest guest Posted January 21, 2004 Report Share Posted January 21, 2004 Hi Deanna, I like your welcome and your introduction and would like to offer my friendship! I am 43 y/o women married, no children and live in Wisconsin. I work in a hospital clinic, indirectly providing care for arthritis and rheumatology patients. I had my first acute pancreatitis attack in the summer of 2000 while having open abdominal surgery for multiple pockets of abscess (as a result of pelvic surgery a month before). The pain from that attack never completely resolved and after three years of diagnostics and further surgery, it was found that I have obstructive pancreatitis concomitant with pancreas divisum. I have had 4 ERCPs since Sept 2003, with two sphincterotomies and 2 stent placements with the final ERCP doing a dilation of the minor duct. Because of various problems with my pancreas doctor I decided to terminate our relationship so I am currently being followed by my pain doctor only. However, my recent GI doctor has put considerable doubt in my mind concerning the accuracy of his diagnosis. He was adamant in September that I had " classic " obstructive pancreatitis that is associated with PD but on my last visit a few weeks ago, he backtracked and stated that he was most likely wrong and that I do not have a pancreas problem at all, unless he caused it by all the ERCPs and stents. Currently, I am doing an experiment that I call " mind over matter " - that is, I am trying to taper off from all of my medications in order to assess where I am at with my pain levels; to see if the stenting provided me with significant relief and if my background pain will lessen as I heal from the recent procedures. My opinion at this time, is that the stents " cured " the subacute condition associated with the blockage but has not affected the pain that is associated with the ongoing pancreas inflammation. I have not received any information from my former GI as to the condition of the pancreas as seen by EUS and ERCP so I am unaware if I am battling pain due to chronic pancreatitis or from other causes related to the abdominal surgery (scarring, adhesions or nerve damage). I also understand that pain from chronic pancreatitis can arise years if not up to a decade prior to detectable changes being seen by these diagnostic procedures - so I am not sure what significance to place on a " nomal " EUS or ERCP if that is what they showed. My decision is to assume that I am feeling the effects of a sick pancreas and that these symptoms will be chronic and most likely progressive (a " hope for the best, prepare for the worst " attitude). Therefore, my goal will be pain management, not a total alleviation as it seems that there is no simple answer for diagnosis and treatment of benign pancreas diseases. Any opinions that you would like to express or information that you think will help me plan a course of action will be welcome! Thank you for the time that you are spending to met and greet all of us! Laurie Quote Link to comment Share on other sites More sharing options...
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