I have been hospitalized four times in last two years. Finally I met a doctor in UK who prescribed Asacol Foam Enema. I was unable to get into remission for last so many years with all drugs, however, with this foam enema, I got in full remission in just few weeks. I was surprised to find that drug industry that makes Enemas for UC has been dominated by company that makes Rowasa Enema (Israeli Company). I am shocked to find that Rowasa has complete monopoly over this industry.
I've had UC for 18 years so I understand from mans point of view and can't stand thinking from a Women's or child. I first have a quick question, is she taking the Prednezone for the bleeding? I know when I go into a flare and the bleeding is bad I go on a regulated decline dose to 0. Now some start a lot lower than me but I have to start a 70 mg then decrease by 10 mg every three days until it stops.
Has anyone tried Lialda? Does it perform any better than Asacol? How much more is your co-pay for Lialda than Asacol. I want to ask my doc to make a switch.
I have noticed that my asacol is not breaking down and is being passed in my stool! Is their a reason for this? What can/should I do?
He was switched from Asacol to Pentasa when his liver enzymes were slightly elevated. He was on a steroid for the first 2 years after he was diagnosed. He hasn't been on a steroid since 2006, when he was diagnosed with Diabetes. The Steroids are more for the flares, the Pentasa is used more as a maintenance drug. He is also on Purinethol, which is chemotherapy agent, to help decrease abnormal growths. Good luck.
i was prescribed asacol 2x 400mg, 3 times a day for two weeks. after this time i was also diagnosed with CKD at stage 3a with a GFR of 53 and a creatinine clearance of 87.14ml/min.
i took asacol again for one month at a reduced rate of 1x 400mg, 3 times a day (3-4 tablets recommended for prevention of relapse).
then i stopped taking it for 2 months.
i took asacol again at 1x400mg, 2 times a day for 2 months.
A related discussion, <a href="/posts/Gastroenterology/Asacol-800/show/1876778">Asacol 800</a> was started.
I have a NEW G.I. doc who keeps referring me to a colonoscopy and an MRCP before she decides to do anything but I've had a flare-up of UC for a month and need some relief. Today I saw a whole Asacol HD tablet excreted and the G.I.doc said "that's ok--it's still absorbed." Ok--so now I must be reasonable and ask a question as how is it absorbed when NONE OF IT--repeat, NONE OF IT---is degraded at all? This woman doesn't get it. Anyway, what should I do now?
Is there a program where my son can get help with his Rx for asacol? He does not have insurance.
t poop for over a week...and every time I get rid of it, via enema or laxative, it comes back again a week later. Sometimes I'll even have diarrhea before I get constipated again. Right now I haven't gone in almost a week, again, and all my doctor tells me to use is Miralax or a stool softener. Both have worked OK in the past to temporarily fix the problem, but today, I got severe nausea and cramps with really sharp pain in my stomach.
I did a flex sigonoscopy and the GI said it is a 95% chance it is ulcerative colitis but the samples he took we would have to biopsy and confirm the other 5%. He recommended that I start on prednisone ( a steroid) on a low dose asap. I do not believe this is the best option for a pregnant woman. So my questions are; has anyone ever see a pregnant woman get her first flare up while pregnant? Why would they suggest prednisone for a pregnant woman? Is this safe at all?
Had coloscopy in August-showed some mild inflammation in ilieum and rectal area-was put on Asacol. Asacol helped the rectal pain but RLQ pain continued. Went back to ED in Nov for severe RLQ pain. CT and bloodwork normal. I had changed from Asacol to Pentasa the week before and the rectal pain had come back-significant burning pain. Went to another doctor and had more bloodwork-borderline IBD tests. Went off Pentasa for a few days in Dec and had severe RLQ pain and right hand pain.
A family friend (who gave birth 35yrs ago) said that before she delivered she received an enema. Do they still do this?? She also told me morning sickness starts in the second trimester and i definitely know that is wrong lol.
My mom told me that in the hospitals Some of them give you Enemas and I really don't want one!! Unless I for some reason need one, but she also said they do it as a precaution so the baby doesn't swallow or breath in BM. I'm all for it if it Needs to be done for her safety but I'm not sure about it.. Any stories or advise.
Has anyone had to use a enema or went to the er and had one done? Should i try it myself or go to er? Does it hurt? What should i expect? Im really nerves and kinda scared :( never had any of these prob. Be4 and this is all new to me..
No enema
Self-administered or given by nurse
If constipated at onset of labor
To start or stimulate labor
At times, enemas have been able to start contractions. Doctors or Midwives might want an enema performed to help stimulate or speed labor. The decision of whether you will or will not need an enema should be discussed with your doctor or midwife during one of your prenatal appointments.
Try to stay away from dairy, alcohol, grains (have rice instead). If you can figure out what triggered the flare, that would be helpful so you know to avoid it in the future.
She is 13 and has been diagnosed with Crohns/ulcerative colitis. BUT...she cant take any of the medications, like pentasa, asacol, 6mp because she gets pancreatitis and becomes even more sick. So I have worked in a hospital pharmacy for 15 years and I put her on fish oil, probiotics, calcium and her symtoms were half relieved. She still has some bleeding and lots of diarrhea, but she has not been hospitalized for 3 months.
So my question is were to now.
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