I was diagnosed with UC 2 years ago. (I had mild symptoms with our first child...cut to 10 years later, after our second child, and I end up in the hospital.) My GI told me that UC is often "triggered" or "activated" after giving birth. Steroids (I am looking at you Prednisone) gave me 25 extra pounds to lose. I have 10 to go, and wouldn't you know my insurance decides not to cover my Asacol anymore. 1 week off the meds and I am in a mess. I started Lialda last week, and hope I can get things under control without the 'roids! Has anyone noticed symptoms of UC or other GI issues in your children? I as because my, now 3 year old has had tummy issues since he was born (allergic to breast milk, lactose, bad diapers...) I wonder if it's worth mentioning to his pediatrician that I have issues?