All other tests and antibodies were negative, SED rate was normal, liver and kidney chemistries normal, C-reactive protein normal, no anemia, CBC normal, etc.
Doc wants me to start Asacol but the side effects seem worse than my mild diarrhea. Question is, should I take the anti-inflammatory to try and stop the autoimmune process? The rheumy thinks this could progress to Crohn's, Colitis or autoimmune hepatitis someday.
I'm thinking about consulting a naturopathic doctor.
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.
Does Crohn's disease affect an hepatits c antibody test... and if so how long should you wait to be tested after exposure? Exposure was through a sub q needle stick at work... i was wearing gloves and got tested 7 and a half months after it. Negative results but I have had crohn's disease for at least 2-3 years... I am currently taking ASACOL HD 800mg 2 tabs twice a day.. i also have ulcerated colitis... I have ocasional diarrhea nothing to bad.
I enjoy the Lialda because I was taking 3 pills three times a day with Asacol and now I only take 4 pills once a day with Lialda. I haven't been on the Lialda for very long, but so far the results are good. I'm not sure that it is better than Asacol, but I think it is easier and equal in performance. You might ask your doctor if they have any prescription cards for Lialda. My doctor was given cards from Lialda, which you can use with your insurance.
I started Asacol almost two weeks ago, and it worked very well after a couple of days, but after almost two weeks, I got very weak, dizzy spells, fatigue, like the flu. It's been five days, and most of the time I need to lay down. I couldn't go to work today. When does it stop? I stopped the medication four days ago. It was for colitis.
Hello all,
I have Crohns disease, and for about a year have been having some abnormally high liver function tests. The Dr. is changing my medications a bunch (off Asacol, reduced Imuran, etc), and I have abstained from alcohol use (not heavy drinker, but partied hard when I did), but my liver counts have not decreased significantly. I am wondering if my daily Marijuana smoking could be causing the elevated liver functions, rather than the medications or something else.
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.
s disease, carcinoid syndrome, intersticial lung disease and sirosis of the liver. I had a colonoscopy done in Boston a month ago and learned that all the pain I have been having in my stomach (which they kept testing me for diviticilitis (sp?) for the last year was in fact Crohn's. I am learning as much as I can and am on antibiotics right now for another flare up. My doctor is going to put me on Azechol (not sure of the spelling) and he said it is a good medication.
You're the boss, not him. You also have a duty as a parent to make sure he is healthy. By saying 'I can't do anything' you effectively are neglecting your child. If you can't protect him, perhaps the state should. They will do what you won't. It seems, you need to put your foot down and get serious about his health. It sounds like he's extremely ill and has liver disease along with cardiac disease and a list of other ailments.
she is suppose to be having her tonisls and her adnoiods out in 2 days and now they tell me something in her liver is up they have her on imuran, asacol, and prevacid. but her last test were fine and now they take it again before her surgery and don't know if they can do it . so have to go tomorrow to get more test done. can anyone help me understand what could be going on here..
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.
The idea is to get off the steroids asap but make sure the bleeding is stopped. The other thing is to increase the Asacol right away to get the UC under control and adjust her dosage to manage it. If she is still having trouble then she needs to treat it from both ends, so get her GI to prescribe an enema nightly with her regular Asacol orally but it's very important to get her off the prednezone. It's bad taking it continuously.
The Gastro doc wants to treat me with Asacol, but I am suffering from CKD GFRaround 45%.......I told doc and he said ok entercort would be the alternative. that is also an issue as i am a diabetic I have read that just taking imodium and fiber works quiet often also pepto bismol is this correct, Immodium is what i have been using for the last four years any where from 1/2 a pill per day to 1 pill depending if I have not had a movement for day then i back off until I do.
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.
My son was smoking pot and was feeling better with it. He is alergic to sulfa medications and the Asacol resulted in Pancreatitis. Unfortunately most medications for UC are sulfa based. He also has g6pd, a blood difficiency and Gilber's disease. He has been on 6MP and the doctors are now talking Remicade.
It has now been 8 months of frequent bloody/mucousy stools and no relief. I have been on Asacol, Sulfasalazine, and most recently Lialda which I had a bad reaction to. Nothing has improved my symtoms.
I recently started seeing a new GI and she retested me and I am positive for C diff. She also tested a ANCA-IBD P-ANCA Titer recently that came back negative.
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