I took my first dose on 5/22. It's now 5/31 with no improvement. Any intermittent improvement I've seen is, I think, due to the cortisone enemas.
I haven't felt this bad in a long time but oh man I really was hoping to never have to use pred again
My GI gets back from vacation on Tuesday and my guess is that he'll recommend prednisone. I probably would have already given up on Uceris if it weren't for the fact that pred will take a week to kick in for me.
Anyone out there have a really delayed response to Uceris?
dx 4/09 (1 week before breast cancer dx) with mild to moderate UC through mid-transverse colon
4.8 g Lialda; cortisone enemas nightly
RenewLife Ultimate Flora 80 billion; L-Glutamine; Florastor
Gluten free since 8/12 + in remission since 9/12
5/8/13 ate gluten & began flare
5/22 began Uceris