Disclaimer: Forgive me posting this in Cat General, I just feel better sharing this here.
I went to my doctor for my follow up appointment after my hospital stay (11/3-11/5) yesturday. I've been feeling pretty horrible, despite having a new wonderful job, although I know I may be stressed with wanting to be perfect.
He upped my dose of Pentasa, the medication made for Ulcerative Colitis and Crohn's Disease from 8 pills daily to 12 pills daily.
That isn't what freaked me out though. He added a new medication for me, Entocort EC (Budesonide). I'm taking three 3 mg capsules each morning for at least a month, then we'll taper my dose down after that. He said the standard dose it 3mg (1 pill). Entocort is a steroid, but with fewer side effects than Pred. Its made specifically for Crohn's Disease, so that's kind of neat knowing it was made for my health issues.
I'm kind of worried about the possible side effects though. It can cause weight gain, something I've never had to deal with. It also greatly decreases your immune system. If I get sick, I'll get it worse and then that usually causes an attack. I decided that last night I'm going to make sure my butt is in yoga at least twice a week, I'm eating super heathy and taking all my vitamins.
This will bring my pill total to 16 pills a day. Not counting vitamins and iron. Its time for a new pill holder thingy.
I got to see the results of my CT scan too. That was interesting. I haven't advanced much, so that's a good thing.I also saw part of my chart my GI has for me while he was making sure my pharmacy not only had my medication, but to check to see how much it would be with my insurance. (Have I said yet today how much I love that guy??) I guess he does a write up on his patients after each visit/hospital stay. It said "Kelly is a charming, 26-year-old young woman..." Charming?? How sweet!!! Especially since patients don't usually see their own charts.
All in all, he's a bit worried about me. He says that based on the biopsys they took two years ago, I shouldn't have this much pain. He talked about Remicade, but said we want to have options in the future. (Its an IV treatment that will make you feel better, but you can only have it like 3 times in a lifetime...and I only have 1 of those!)
Anyway, I just thought I'd update you all.
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