All of these medications have been reviewed by a combined several hundred patients who have Ulcerative Colitis who use this site.
Below are the pages you can click on to read the actual reviews about the experiences UC’ers had with the medications listed.
AND, if you would like to add your own review of your experience, there is a button on each page where you can do just that.
- Prednisone –
- Remicade – https://www.ihaveuc.com/remicade-reviews/
- 6-MP – https://www.ihaveuc.com/6-mp-reviews/
- Lialda – https://www.ihaveuc.com/lialda-reviews/
- Pentasa – https://www.ihaveuc.com/pentasa-reviews/
- Asacol – https://www.ihaveuc.com/asacol-reviews/
I hope this information is useful to some of you who are in the decision making process and deciding on which medications to use to treat your UC.
And One Final Thought:
If you are feeling like there are no options left for you, especially if you’ve used all the medications you’re willing to try out, there still are options.
I myself was in that position several years ago, and I felt like my only option was surgery. (Make no mistake, surgery for almost everyone who goes that route is VERY happy with their decisions, and you can read the proof of that within the surgery survey we conducted here: https://www.ihaveuc.com/26-colitis-surgery-patients-survey-results/)
But, in the end, I realized that a perfectly reasonable option for me was changing my diet to one which my body could tolerate. And there are many other options that you can investigate as well. Options that are talked about right here on this site. I’ve setup a page several years ago which lists stories from other UC’ers that is dedicated to “Alternative Medicine”. I’ve never liked the name “Alternative” since for people who are using these techniques successfully, its much more than an “alternative”. But anyways. You should check this section out too: https://www.ihaveuc.com/category/specific-carbohydrate-diet/alternative-medicine/
Best to all of you.
So far there’s over 265 participants (and 31 pictures submitted!!!!). Pretty cool UC’ers…ONCE AGAIN!
Hang in there if times are tuff, symptoms do go away,
I started site and the eNewsletter(you can join that below) shortly after being diagnosed with ulcerative colitis in October of 2008 with severe pancolitis (when my whole colon was inflamed).
For me, it was a very rough start with severe symptoms. Getting bounced from medication to medication was not easy or too helpful. But, I did meet another UC’er, changes several parts of my diet, and of course the rest is history.
Leave a comment, ask a question, take advantage of our past experiences here, use the search boxes, they are your friends to0:)
Remember while using the site that:
UC symptoms and flare ups don’t last forever and no two people are the same.
You cool with that? good!
now get on our newsletter so we don’t forget about you.