I was diagnosed as having UC in 2009, started on a mesalamine enema which worked wonders. I weaned myself off all medication and lived a happy UC-free life till 2011. Late 2011 brought on another flare, which I assumed was due to the stress of planning a wedding ( got married January 2012) and not being on my meds. My fiance was terribly worried, but supportive. I assumed that since I had led a med-free life for two years, the same would happen again. But that was not to be. Two weeks after the wedding I had my third flare, but again I assumed it was due to stress (we were relocating to the US from India) and being irregular with my meds. Last month I flared again and that's when hubby and I started reading extensively about UC. I saw a GI in Texas who told me that based on my previous colonoscopy results he felt I had Crohn's and not UC. But could two biopsies be wrong? My main question (sorry for the rant) is we're just realizing that I could give UC to our kids. All the reading I have done is about parents whose children, some newborns have been diagnosed with UC...which is heartbreaking. I want to know, are there parents out here whose children do not have UC or any other form of IBD? My dad has Behcet's syndrome and I don't know whether this would increase my risk of passing IBD on to my kids...Any advice would be much appreciated..