Abdominal Adhesions
So for the past 3 months I have had awful middle epigastric pain, new onset constipation, no appetite at all, dizziness, headaches, and horrible itching. The pain came on suddenly in the middle of the night that woke me up from a deep sleep. So far I have had an upper GI barium swallow study, EGD and colonoscopy, 2 CTs, 1 MRI, X-RAYS, and an exploratory abdominal surgery where I had a few adhesions and a cyst on my left ovary. All of my lab work has been fine and all of these tests have been normal. Anyone have any suggestions on what it could be? I am seeing my GI tomorrow in hopes of scheduling an ERCP and if that doesn’t show anything I will be headed to the Mayo Clinic. I’m open to any suggestions on what y’all think it might be.
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Since being diagnosed with chronic pancreatitis, I have had probably 15 therapeutic (stints placed, removed, balloon clean outs, etc...) ERCP's and have yet to have one cause an acute P attack. I do go to the medical school hospital in my state where there are very high volumes of these procedures done. That would be the only thing I would recommend about the ERCP; you do not want to be the fifth person the Dr. has ever performed one on. Good luck and I hope you find some answers.
No. I have been off work since mid December. I can barely unload the dishwasher without having to stop because of pain.
I could always get one done at OU med school. That’s our #1 hospital in OK
Thank you! And no I haven’t found anything that helps with the pain
@medic_simmons, have your doctors ruled out complications from interstitial cystitis?
I'd like to tag @suzettemh @susierq111 @tbeckys @cbs61752 @kas1792 @operationqueen @rdrdhap @suzette @barb54 @8dzaweek @lexi @jeananderson2014 @mgnunez75 @Weedy @praymond234 @mogulers @kerrilynn1 @jmgm @charlenem, who have all shared their IC experiences on Connect, and invite them to join us here with any insights that may help you.
You can also read through some of the conversations in this discussion:
https://connect.mayoclinic.org/discussion/i-ve-been-told-that-interstitial-cystitis-is-an-autoimmune-disease-are-there/
@kanaazpereira no they have not. They haven’t even mentioned it. I will have to bring it up with my urologist. I’m calling to make an appointment as we speak. Thank you.
I know this is gonna sound weired but does it somtimes feel like you got rocks in your stomach
Maybe gastroparesis.
Hello @medic_simmons,
I was wondering how you are doing. Have you had any new diagnostic tests and/or procedures scheduled yet? I do hope that your doctors are able to get to the root of your problem.
I would love to hear from you again and know how you are doing.
Teresa