I have chronic pancreatitis from a medication I took. Have had 2 hospitalizations with acute pancreatitis. Pancreatitis isn’t fun!!!!!! The worst pain I’ve ever had. Now just have to watch what I eat, especially no greasy foods. Also took Creon for a while but it made symptoms way worse for me. So not on any meds. Hard disorder to treat.

I don’t know anything about calcium deposits but am curious why you were tested for EPI? Did you have the traditional symptoms for that - loose, greasy stools? Is that what lead to an MRCP or was that because of something seen on the CT scan?
Those of us with chronic pancreatitis often take a PERT, really limit fats in our food intake and will agree that it is life altering.

I have no idea and I don’t have any episodes. That is what makes me think that I don’t have it.

I have all the above tests and they determined part of my pancreas had atrophied, but EPI was not diagnosed until I had a poop test and my reading came back at 129 for enzymes that shoould be in the nromal range of 200-500 is normal. Have you had that test?

I am wondering if your lipase or amylase levels are elevated and if anyone has checked you for autoimmune chronic pancreatitis. The doc doing the ERCP may have seen something in the scope that radiologist didn’t see on imaging, hence the discrepancy. It’s always confusing when different docs say opposite things. That’s where your own research can come in handy.