So my Doc from the Chron's and Colitis center contacted me back about Cellcept. I may need to go on it for my Kidney's and was hoping it would help my UC too if I did take it (I would have to be off aza, can't be on two immune suppressors at the same time). Doc says that it helps out 25% of people w/UC and that he would want me to try that before trying remicade. At least it's another option.....
Just wanted to throw that out there to others who may have tried lots of drugs that have not worked for them but not cellcept. Maybe discuss w/your GI.
I try to look at the small percentages and think ok I can look at this one of two ways. I am in the small percentage of the poplulation that has UC, I am in the small percentage of people who cannot take 5ASA's.............etc. anyhow.
Hope everyone is doing well. I am at 5mg for two days and 2.5mg of pred one day. I then will go to 5mg then 2.5mg alt days for a month. super slow taper. I seem to get a tiny amt of blood about a week after each taper but then goes away. Please wish me luck, I hope to be off of pred in 2.5 mos 2 days, 3 hours and 47 seconds, but who's counting???????..........moi?
Beth, 32 ~ hoping to taper pred successfully, wish me luck!
Major Flare Sept/Oct 07
UC dx'd 03/00 (Proctosigmoiditis); Pancolitis since 09/07
Azathioprine 200mg 1xday nightly; Calcium and Vit D 500mg 3xday, Multi Vit, Folic Acid 400mg 2xday, Prilosec, Probiotics.
Minimal Change Disease (Kidney Disorder) dx'd 09/07 - partial remission since 03/08
Prednisone 5mg 1xday, Simvastatin 20mg 1xday, Diovan 160mg 2xday. Tekturna 300mg 1xday, Fosomax 70mg 1xweek. MCD may be from hypersensitivty to 5ASA drugs. Do you have edema? If so, check your blood protien level!