Alexandria is not diagnosed with UC at the moment, but she’s worried she might have it and being only 18 years she’s super worried that her life is just not going to be everything she expected moving forward. Life sure goes on, and all sorts of great things can happen UC or not, so give her a read and a comment to help her through!
Natacha was recently diagnosed, scared as hell to change her diet, and a self proclaimed nail-polish freak from Canada.
Scientists are making some MAJOR news this week with the releasing of data linking gut bacteria imbalances to Crohn’s Disease which is another member of the IBD family. LOTS of reasons to be excited about this new science.
LEARN HOW Scott has spent years working on never having his UC stop him from doing anything…including hiking, biking, and just about anything else. It’s an incredible story!
My grandson has been diagnosed with UC, he’s in high school, and he is trying to figure out what foods work best in the early stages of diet treatment.
Find out why Olivia (who’s 19 years old from near London, UK) is so happy about getting control of her UC symptoms and being able to move on with life on her terms!
This terrible disease has given me the ability to truly see what I have. Colitis may have taken away some things, but it isn’t permanent, and this knowledge combined with my new ability to appreciate all of the other amazing things that I have going for me is my greatness.
Find out what Kim is doing to put an end to the 6 years that have taken place since her diagnosis. She’s finally got a new plan to attack the colitis symptoms, and she’s looking for 2014 to be a breakthrough year.
Ashley’s having a really hard time explaining UC to other people including her family members. These others just don’t seem to understand what its all about. What’s your solution to talking with others about UC?
Is there a relationship between bone loss and having ulcerative colitis, or is there something else going on?