Monday, July 28, 2008

Doctor Update

A recap: Very painful Crohn's flareup right now. Had to go to the doc on Friday afternoon. Here's what happened...

So, he confirmed that yes, indeed, I'm flaring up. Duh. So, he gives me medicine. First one: 500 mg of Pentasa, two pills, twice a day. Second one: three mg of Endocort, three pills, once a day. He then gave me Vicodin for the pain until the other stuff kicks in (so far, not happening). I now have to call the office this week and set up and appointment for my Remicade infusion. And, I have to go get an endoscope next Monday.


What's that? An endoscope? But I thought Crohn's was in the intestines...doesn't an endoscope go through the mouth?


Yes, an endoscope. Yes, my Crohn's is in my ileum. Yes, an endoscope goes down in to the stomach through the mouth.


It turns out that the last time I was hospitalized (December 2006), they performed both a colonscopy and endoscope. During the endoscope, they discovered that I have an ulcer. An ulcer! Can't ever imagine why!? So, the doc wants to go in and see how that ulcer is doing. Of course, he makes it sound so easy. In the meantime, this is what I have to do:


Hubby has to take a day off work. I need someone to take me to the hospital and drive me home after. There also needs to be someone home to watch the kids. Hubby will do that, maybe bring them to the park or something for a couple of hours. I have to starve myself starting midnight the night before. That means no coffee on Monday. NO COFFEE. My appointment isn't until 11:30! Thank goodness they give me good drugs, otherwise, the migraine that is going to ensue from no coffee will kill me. Once I am home, I will be so out of it. It should prove for some funny stuff. Too bad we don't have a video camera. They will also probably do a biopsy. No reason why, they just like to cut tissue while they're in there just in case. I don't have cancer. I think they just like to cut and make it hurt.


So, this is my life right now. Popping pills, laying in bed, feeling bad because I don't have the energy to take my kids down the street to the park. It's enough to make dinner or load the dishwasher. I do my best, but sometimes, it doesn't feel good

4 comments:

  1. aww im so sorry i wish i was closer to help out

    ReplyDelete
  2. I know how you feel I am just being diagnosed with Crohns. I know how guilty you feel about not being with the kids. So hard. The pain is almost unbearable. I keep asking WHY? Know my thoughts are with you.

    ReplyDelete
  3. Our stomach's could be best friends.

    I'm so sorry to hear of all of the awful news of scopes and pills. I know its no fun. I feel for you :(

    ReplyDelete
  4. I still love you LC :)

    Farts and all !!!

    ReplyDelete