During moderate/sever flare-ups I took prednisone orally, in foam suppository as well as mesalamine orally and through suppository. In moderate flare-ups mesalamine orally w/ mesalamine suppositories.
My question is - beyond the general risk that HSV presents - how additionally risky is this for me? It is a possibility that at some point I will have a flare-up that will require immonusuppressive therapy. If I was to contract HSV could my UC symptoms become more severe?
Being how I am getting random muscle aches and hives on my body, and my armpits itch and get hives as well that go away within an hour or two I grew increasingly worried. These symptoms are reported by folks that suffer with IBD as well.
I performed a Oraquick test which came out negative at 5 weeks. Then I went and got a Gen 4 HIV 1 & 2 blood test done on Dec 6th 2017 which came out negative.
If it is not effective, then other medications like steroids, mesalamine and bismuth subsalicylate may be tried.
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The information provided is for patients’ education only and is not a medical advice. Always consult your personal physician for complete evaluation of your health problem.
- Ratnakar Kini M.D.
Her gastroenterologist started her on Mesalamine (4 capsules daily) and later added prednisone 100 mg enemas to try and get the flare-up under control. Things are getting better and she has some of her strength back. There is one puzzling thing that the doctors are not able to pinpoint. This is an intermittent fever that starts in the afternoon and lasts to the night. In the morning the temperature is back to a low 97 degrees fahrenheit and stays stable until afternoon below 98 degrees.
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I am talking about a girl from Poland who posted here on this forum and on other forums ..
My recent result of biopsy after the colonoscopy indicates epithelial dysplasia. My doctor just advice me to continue taking the mesalamine (Asacol) Do i need an another urgent medication/treatment for dysplasia? What should be my next move?
What is available? Are there any interactions with boswellia and mesalamine that I should be cautious about? Are there any precastions about its use?
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?
What other symptoms are present? Mesalamine or Canasa suppositories works by preventing the production of substances that cause the inflammation of the colon. The usual side effects include diarrhea; dizziness; gas; hair loss; headache; mild stomach discomfort or pain; and nausea. The sour taste could be indirectly related especially if you have other gastrointestinal issues like acid peptic disease or gerd.
Interesting that LDN shows up in IBD treatment! Looks like a serious alternative to the traditional steroids and immunosuppressives and NSAID's. A treatment that doesn't harm the liver.. I'll definitely be looking into this. I don't imagine that "old school" GI's are big fans of LDN however. We'll see. I'm not a big fan of NSAID sides.
I had UC for ten years and then my bowel perforated and I required a colectomy. A year later I had the J-Pouch surgery and have done very well since - 15 years. Are you going to be having that as your next step? Yes, UC is nasty. My son is now suffering from it too.
It will get better. Did your doctor send you home with any prescriptions? Drugs like Loperamide can help with the spasms and diarrhea. Gravol will help with the nausea.
t get bad. I had ulcerative colitis for 10 years before my bowel perforated and I had surgery to remove it and then had an ileal pouch built. My son has severe ulcerative colitis but it is in remission with Imuran. You need to see a different GI doctor. Here is some information on treatments for you - I've added a couple of notes:
Dietary Restrictions: Iron supplements may offset anemia caused by ongoing blood loss in the stool.
She again had colonoscopy and histological examination inferred that it was ulcer. She is being treated with Mesalamine and now she is well. Please check with your doctor.
The periods of remission can last from weeks to years."
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Springer - Mimics of Ulcerative Colitis...
"Infectious colitides such as Clostridia difficile, hemorrhagic E. coli, Campylobacter, Aeromonas, and Salmonellosis can often present as severe ulcerative colitis. Other infectious pathogens, which also need to be included in the differential diagnoses, include Amebiasis, Shigellosis, Cytomegalovirus, and Rotavirus.
This all occurred after starting a 30 day course of Canasa (Mesalamine) to which I had rash and breathing problems in what seems to have been an allergic reaction and possibly triggered the above problems.
I am now on Claritin (10mg), Lexapro (5mg) and Aciphex which together brought relief to stomach pain within hours.
Cardiologist sees no Eosinophilic infiltration or Loeffler’s.
Repeated Endoscopies show no problems. I am negative for Eosinophilic Gastroenteritis.
I have Crohn's also. I'm pregnant with my second child and have not had a problem either time. However, my doctors did tell me that if you're Crohn's is under control when you get pregnant, it's likely that your condition will stay the same or get better during pregnancy. If you're having a flare up or the disease is not controlled well when you get pregnant it will likely get worse.
In terms of medication I would trust your doctors here.
I contacted my doctor and his guess was that the powder worked topically in the digestive system and the alcohol is metabolized by the liver and therefore does not work as well. I contacted pharmacies and the drug company themselves, and there is no date know for when it will be available again.
Is anyone else experiencing this? Have any tips, I'm pretty new to this. Or is anyone taking a different medication and getting good results?
Hi,I've been diagnosed with ulcerative colitis yesterday and was given 30 x 500 mg suppositories but the consultant said I would have my next appointment in 3 months time.I have to use one per night.Do I use them just for 30 days or should I ask my doctor for some more after 30 days ? It's all very new to me.Any advice would be appreciated.
I had begun taking medicaton (back then Pentasa), and after a month and a half stopped taking it because it seemed to irritate me more than anyhing else -at first it had cut diahrrea quickly. But it began irritating me (my stomach I think, and my intestines).
Being averse to taking drugs unnecessarily, I stopped completely and never suffered from UC again until 8 years later and the flare up did not occur 'spontaneously'.
Not any of those will delay seroconversion.
been quite bad with a few painfull flareups lots of blood etc/ currently on pentasa and steriods at the moment/ started the pentasa last tuesday after a bad flareup/ just wonderd if any one could tell me there experiance on pentasa , and how long they took to work ?
Hi, I am 23 years old and am currently in a flare up that started back in November 2009. I have tried Mesalamine, Prednisone, 6MP, Remicade, and am currently taking Humira and Methotrexate once a week. I feel like my life has been taken away from me. I was studying abroad for a master's degree when the flare up set in and decided to fly home to my parents to get proper health care and support.
They are all different names for Mesalamine. So they should all be the same formula and work the same. I know from experience that sometime the brand works better than generics, but thought I would share this information with everyone.
I was told I had diver and given cipro and flagyl and told to go home. About a month later I went for another CT scan and I was feeling better. The doc called me and said there were no changes on scan and gave me same meds again. That night I thought I was having a stroke or heart attack. Went to ER and was told I was allergic to Flagyl and to stop taking it. Was sent to Gastro Dr and she said there may be a tumor on my CT.
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