Ive been on prednisone ever since I was first diagnosed with a severe Crohns this summer. I've tapered down with lots of hiccups, was finally down to 5mg. At that point I was scheduled for a capsule endoscopy which screwed me up completely! My crohn's is mainly in my colon and rectum, so awful! And just in time for Christmas I am back up to 40mg prednisone! So frustrating. So next in line seems to be going on Humira after all.....but for now, I am wondering, how do prednisone versus entocort effect you? What have been the side effects? This time around even 40mg of prednisone doesn't seem to work as well as it did the first time around, I'm in pain most evenings and night. The doctor I see mentioned entocort, but I chose to stay on prednisone, simply because I knew how I text with side effects to prednisone, I'm only experiencing the sleeplessness.....but I am now wondering if entocort would maybe help my pain better? Just afraid of side effects.....
Thanks! Happy holidays!