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Flare up with proctosigmoiditis
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Ulcerative Colitis
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Aiden873
New Member
Joined : May 2012
Posts : 1
Posted 5/17/2012 7:03 PM (GMT 0)
Hi everyone!
I was diagnosed with proctosigmoiditis back last September. I was prescribed an enema and told to take 2 tablets of Asacol 3 times a day (6 total). I stopped using the enema a month later, and more recently, my doctor told me to decrease to 2 tablets of Asacol 2 times a day (4 total) and then go to 1 tablet of Asacol 2 times a day (2 total).
Unfortunately, since doing that, my symptoms have started to come back (mild cramping, feeling like I have to go multiple times a day, not much coming out, etc.). I called my doctor and he told me to go back to 6 total tablets in the day. However, that has seemed to have little effect, as my symptoms have continued and appear to be getting a little worse. I'm waiting for him to get back to me, but it might take a week or so before I go in to see him.
Does anyone have any other advice for me to do or try? I appreciate any suggestions. Thank you!
i_love_coffee
Veteran Member
Joined : May 2010
Posts : 637
Posted 5/17/2012 7:05 PM (GMT 0)
get back on the rectal meds asap!
kazbern
Veteran Member
Joined : May 2010
Posts : 8384
Posted 5/17/2012 7:22 PM (GMT 0)
I agree.
In general, I think the idea of tapering the oral meds is not good, although you can probably get to a "maintenance dose" - probably more than the 2/day.
I think you will need to use a rectal enema for a lot longer than 1 month to get total remission in the rectum.
quincy
Elite Member
Joined : May 2003
Posts : 33769
Posted 5/18/2012 5:12 AM (GMT 0)
ditto...the doctor shouldn't have had you stop the enemas. Do you have a prescript
ion that has refills?
The maintenance dosage of the asacol could be 4, but probably 6 is best if your sigmoid is involved.
q
hateuc
Veteran Member
Joined : Jun 2010
Posts : 2361
Posted 5/18/2012 12:29 PM (GMT 0)
Def. agree w/ rectal meds!
SWA
Regular Member
Joined : Apr 2012
Posts : 27
Posted 5/19/2012 10:47 AM (GMT 0)
I used a mesalamine enema for a while and it didn't really do anything for me. I recently saw a specialist who started me on cortifoam. It's a steroid based foam enema, much easier to retain in my opinion. I've been taking that along with a suppository 3 times a day for about
a week now and the results have been pretty darn good! This doctor was also the first one I've been to that admits diet is huge in controlling the symptoms of UC. So between the diet changes I've made and the meds its getting much better. Thank god, because I felt like death for a while.
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