- Joined
- Apr 10, 2012
- Messages
- 9
Ok a little background info (probably more than you need): I've had crohn's since 2008 but it has been mostly in remission since around 2010. Last November I started having stomach pain (bad). It didnt feel at all like my Crohn's disease. I didnt have health insurance at the time so I told my doctor to pick one test and I would pay for it. Had a CT done, which showed nothing. We opted to do a round of antibiotics just to see if it would help (thinking maybe H.Pylori or something). Antibiotics did help and we did a second round just to be sure. January I get health insurance and we do my colonoscopy/endoscopy and everything comes back normal. Crohn's is in complete remission still.
Fast forward to June and I start noticing some minor stomach pains again. Wrote them down to track them but wasnt frequent enough to bother doctor. July they become more frequent and I make an appt but they cant get me in till end of the month (my doc is on vacation). This Monday pain gets really bad, fit me in with another doctor at the practice who say he wants to do an MR Enterography. I agree, not realizing it requires oral contrast. I have an obscenely hard time with liquid medication of any kind. Always have. My mother says I even threw up as a baby when she tried to give me meds. I started on pills around 3.
MR Enterography tech informs me today it is 3 bottles of contrast. When I had my CT last November I made it through one and a quarter bottles before the tech took it away because she couldn't stand to watch me anymore as I gagged, choked and cried trying to get the stuff down. I call my doctor's office freaking out because I knew I cant get through 3 bottles. Doctor says its really the best test and I need to try.
I go online and discover there is another test: MR Enteroclysis where they administer the contrast through an NJ Tube in the nose. This sounds great, I relax, I call my doctor thinking everything is going to be ok. Nurse calls me back and informs me no one does the MR Enteroclysis test. Back to crying again.
I'm freaking out and my test isn't even until Tuesday. I know I'm being a baby and its probably all in my head but when I say I would be happier having them shove a tube through my nose down my throat and into my small bowel to administer the contrast, it gives you an idea of how hard liquid medication is for me to take. I'm honestly just considering skipping the test and living with the pain. It hasn't killed me so far.
Does anyone have any advice? Does anyone live in South Florida and know of a location that does MR Enteroclysis? I don't know what to do. :sign0085:
Fast forward to June and I start noticing some minor stomach pains again. Wrote them down to track them but wasnt frequent enough to bother doctor. July they become more frequent and I make an appt but they cant get me in till end of the month (my doc is on vacation). This Monday pain gets really bad, fit me in with another doctor at the practice who say he wants to do an MR Enterography. I agree, not realizing it requires oral contrast. I have an obscenely hard time with liquid medication of any kind. Always have. My mother says I even threw up as a baby when she tried to give me meds. I started on pills around 3.
MR Enterography tech informs me today it is 3 bottles of contrast. When I had my CT last November I made it through one and a quarter bottles before the tech took it away because she couldn't stand to watch me anymore as I gagged, choked and cried trying to get the stuff down. I call my doctor's office freaking out because I knew I cant get through 3 bottles. Doctor says its really the best test and I need to try.
I go online and discover there is another test: MR Enteroclysis where they administer the contrast through an NJ Tube in the nose. This sounds great, I relax, I call my doctor thinking everything is going to be ok. Nurse calls me back and informs me no one does the MR Enteroclysis test. Back to crying again.
I'm freaking out and my test isn't even until Tuesday. I know I'm being a baby and its probably all in my head but when I say I would be happier having them shove a tube through my nose down my throat and into my small bowel to administer the contrast, it gives you an idea of how hard liquid medication is for me to take. I'm honestly just considering skipping the test and living with the pain. It hasn't killed me so far.
Does anyone have any advice? Does anyone live in South Florida and know of a location that does MR Enteroclysis? I don't know what to do. :sign0085: