Guest guest Posted September 25, 2003 Report Share Posted September 25, 2003 Hello again, Right this is my story, I will try and keep it brief!!! I have had abdominal pain pretty much all my life. This was always put down to recurrent UTI's. Looking back now though my pain was always upper abdo pain! About 4 years ago I woke one night (I can still remember the time aswell) with severe pain and feeling really sick. I went straight to the emergency GP and yet again I had a UTI. This pain kept happening and only usaully lasted about an hour but afterwards it felt like I had done ten rounds with Lennox ! I was always sick or felt very nauseas when the pain was bad. Anyway, eventually I was sent to A & E where I was asked if I drank alot of booze! (as many of us are asked). Yes I am only 23 and before this pain started like every other 23 year old I used to go out at the weekend but I wouldn't of said I drunk that much! I was told that I had Fatty Liver and 'sludge in my gallbladder'. Given antibiotics, told I may need my gallbladder out if symptoms persisted. I got admitted to hospital another 7 times (I think) when they decided that all my problems were being caused because of Umbilical Sepsis (I had alot of puss etc coming from my belly button! Nice huh?). I had emergency surgery to remove it and sent home. 2 days later I was back in, same pain but then told I had Colitis from all the antibiotics I had been giving. Finally had my gallbladder out in 2001 after a few attacks of acute pancreatitis. The surgeon told me it was due to SOD and taking my gallbladder may not help! He also mentioned to my Mum about pancreas divisum but nothing has been said about that since and I'm sure if it was that they would have found it in my last ERCP. Last December I had another ERCP and a sphincterectomy (the Dr accidently cut my bile duct aswell during the procedure!). I had eternal bleeding, acute infected pancreatitis and a psuedocyst, and also couldn't breath without oxygen for 2 weeks. I still have pain and nausea everyday and have been told at my hospital that they are not going to try anything else e.g stents etc because of what happened last time. My lipase/amylase are OK (haven't heard that before have you?..lol). They have told me I definately have SOD. I take Dihydrocodeine for pain (not that it helps alot), Cyclizine and Buccastem for nausea, Questran for diahrea and recently been given a GTN spray which also did not help. I have written to some Pancreatic specialists for their opinion (my Dr is a general gastro Dr). I really want to get back to work (haven't worked since Dec) and basically completely fed up! Like all of us in similiar positions. I'm sure I've probably forgotten stuff and if you've read my story before I apologise for putting you through it again! Thanks for listening and I hope I'll be able to help some of you guys in the future. Hope you're having pain free days, Hugs from Shelley P.S I have been reffered to a Pain Clinic as my gastro Doc doesn't think my pain meds are strong enough..my appointment is Jan 04!! Quote Link to comment Share on other sites More sharing options...
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