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Old 09-08-2011, 08:11 AM #21
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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 . It's hard enough dealing with one crazy disease. I'll be thinking about you.
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Old 09-10-2011, 12:44 PM #22
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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.
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Old 09-12-2011, 03:33 PM #23
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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.
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Old 09-13-2011, 07:59 AM #24
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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...
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Old 09-21-2011, 09:33 PM #25
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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.
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