IBD is like MS in the way that it is different for every person. My h has had very good results and minimal side effects from Remicade, a biologic. It's an infusion type drug, not an injectable. Remicade is used in patients with Crohn's or colitis.

My son has been on 6-mp for 5 years and is doing very well. It's not a biologic. My h tried 6-mp and developed pancreatitis from it.

I hope you hear from your doc soon, Barb :hug:. It's hard enough dealing with one crazy disease. I'll be thinking about you.

Started taking prednisone yesterday. They put me on 20 mg, twice a day for five days. Still taking the asacol too. Things are improving already. Seeing specialist on Monday. I will ask him about a taper of the prednisone. Really thirsty (drinking lots of water) and hungry. Trying to keep that in check.

Things are gradually improving. Still experiencing pain but no longer constantly running to the bathroom. Saw the specialist today. Did more blood work to check for Crohn's disease. Gave me a prescription for a different steroid that is used to treat Crohn's (Entocort EC). I have to see him again next week. I am planning on going back to school tomorrow.

I don't think you can take Remicaide if you have MS.

My gf has Crohns...leafy greens and cruciferous veggies really set her off, as well as stress:(
Take care, Barb, and keep us up to date...:hug:

I have had UC for years, they put me in Ascol and it didn't work a lick. I tried fiber...no help either, anti-diarehea meds are a joke. The only thing that helps me get out of an "attack" is Flagyl. (an antiboitic that works for bowels) I don't understand why your doc is telling you to wait so long before coming back..you will end up weak and dehydrated if you are not careful. Maybe another doc? Good Luck. :hug: