So it’s been just over a year since we started posting reviews here on the site with the 5 stars you can rate things with, and a super big thanks to all of you who have shared your experiences with different medications, probiotics, diet, and even the 2 ebooks I’ve written for you.
Whether you’re new to iHaveUC.com or an regular old-timer, I wanted to make sure you all are aware of this truly unique resource that collectively we’ve created for others to read about our experiences.
If you’re interested in reading real deal, the truth and nothing but the truth reviews from other people with ulcerative colitis regarding common ulcerative colitis medications…here are current review pages you can click on to start learning more. AND, if you have taken any of the medications yourself, please click on the medication and ADD your review too so others can read what your experience was/has been like.
The current medication review pages are:
Probiotic Review Pages:
The SCD Diet Review Page:
(Only 1 so far, but it is by far the most popular probiotic mentioned on the site)
Once again, I want to thank everyone who has take a few moments out of your day to submit your reviews on the things listed above. These pages are some of the most popular pages on the site, especially for other UC folks who are concerned or nervous about potentially starting new medications that doctors are recommending. So please continue to submit your reviews moving forward if you’ve taken any of the medications listed.
Also, if you would like to see something new added to the reviews section of the website, please include a comment on this page with the medication you’d like to see reviewed. I’m always more than happy to add new reviews to the site on any medications (or probiotics) or potentially other types of treatments that you might benefit from reading others comments on.
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.