I cut it to a couple of PubMed articles about the genetic connection between MC and celiac, and highlighted the most pertinent sentence on each one. He was very interested, and surprised that he had missed it. He said that my insurance would not pay for a blood test for genes because it would not change the treatment. He thinks he may know Dr. Fine, and said that what Dr. Fine is doing is something he's always wanted to do.
I asked him how many MC patients he has and he said about 20. He said that he has one patient who is a drug addict. This patient will take a bunch of NSAIDS so he can end up in the hospital and get drugged up. Evidently this is a young man because his father has him in drug rehab now. How sad.
I also told him about colonoscopy prep perhaps causing a flare, and he was interested in that. He said that the old Fleet enemas were really bad at causing flares, but he was surprised that the polyethylene glycol would. He thought maybe the magnesium citrate would be more the culprit.
We had a really good conversation, and during the course of it he actually admitted that GIs really don't know how to treat MC right now. He told me I was up for another colonoscopy in 2015, since I had the adenoma, and I did not remind him that last October he had told me that my MC earned me a colonoscopy in three years.
Oh--we also talked about my colon being unusually twisted, and he said that was a marker for IBS. Interesting, huh? He said he often will take a photo of the twisted part, but we looked at my pictures and he had not taken one of me.
So all in all--a very good visit! Thank you all again for your helping me figure out what information to take in to show him!!

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