Good Morning & Evening if you are doing that:))
In the ongoing effort to keep us all informed about colitis related topics, and since so many have a personal interest in diet (OK, not everyone, but quite a few), below are the Study Titles, as well as their associated links so you can read the entire study background and results. Please send these on to others who you might feel are interested, and AS ALWAYS, if you want instructions on how you can search for ANY medical related published study…watch my video here:
Onset of Ulcerative Colitis during a Low-Carbohydrate Weight-Loss Diet and Treatment with a Plant-Based Diet: A Case Report
Influence of environmental factors on the onset and course of inflammatory bowel disease.
Diet and nutritional factors in inflammatory bowel diseases
Dietary protein intakes and risk of ulcerative colitis
The role of dietary fibre in inflammatory bowel disease
OK, there you have them, 5 studies about Inflammatory Bowel Disease, and much specifically on ulcerative colitis. And…of course the diet components. Quite interesting to read some of the ideas, some of which I personally follow, and others which I definitely do not. Heck, I can’t really imagine going vegetarian, but hey, if that is working for some folks, GREAT!
I have had emails for several years now from people who ask me if the ebooks I wrote would work for them if they are vegetarian, and my answer is always a “NO”. Reason being, most of the meals are filled with non-vegetarian foods. So, if you folks are reading today, please take a close look at the studies above, and for a few you may have some new ideas about doing diet treatments vegetarian friendly.
Best to you all,
So I like UC’ers. That’s been going on since 2009 I’d say.
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.