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?
Mary feels pretty strongly that a slight change to her sleeping position made a big difference in getting past colitis symptoms. Even her doctors were shocked. What do you think? Could there be something to it?
Andrew is relatively new to UC, and he’s wondering how often he should have a colonoscopy and if/why he should maybe avoid all western medications to treat his colitis. Check out the story and answers
David is concerned with his health, his bowel movements, even his diagnosis, and he’s wondering when his medications will take effect and when and if he should really focus on diet changes too.