Posted 12/14/2011 2:20 AM (GMT 0)
I have been in a flare for the past week, and my doctor told me I have to go on steroids (prednisone). My family has a history of mania on the drug, and I'm worried that it might happen to me again (trying not to think too much about it). She said it was a low dose (20/day), but if I don't respond to the steroids in three days I will have to be hospitalized and given IV steroids.
I'm scared if I do have to have the iv meds... what's it like?
I was diagnosed in May with UC and I also have Celiac Disease, and while this is only my second flare, the pain is so bad I can't deal with it, I had to go to the er and they gave me 2 shots of duilodid to get the pain anywhere near under control.
The er doc gave me Vicodin but the GI said that vicodin is really bad for UC.
She gave me bentyl which seems to be helping a little, the blood work came back and some test showed levels of being very inflamed or something like that, also that my potassium was 3.1.
I'm super anxious (which I know isn't helping) but I am super worried about being in the hospital for Christmas.
Sorry guess this was more of a vent vs a question