Hey everyone, I was recently diagnosed (19 yrs old, 3 weeks ago). I had been having extremely painful stomach cramps for the past three months and was finally diagnosed a few weeks ago after I went to see the doctor at my school. Throughout this entire period my bowel movements have been fairly normal, I usually go once a day and don't have diarrhea or too much constipation, even during severe flareups (thank goodness). I've just have to deal with a severely painful cramplike feeling after eating meals that usually last anywhere from 1 to 6 hours, and starts either immediately after or 2-3 hours after eating. The only other worrying symptom I have is bloody stool. I'll usually notice some bright red/ maroon blood when I wipe (I don't see blood in the stool in the toilet, but i'm sure there must be some). I had a blood panel and thankfully aren't anemic. Right now the only medicine I've been given is called Levsin SL (.125mg) tablets, which really help with the stomach cramps but don't always last four hours. I'll still have blood in my stool even on the days when I feel perfectly fine after eating (like today). I won't be getting any UC specific meds until thanksgiving when I go home to see my GI doctor.
I was just wondering if people could tell me where I stand in terms of severeness of UC. I lead a very active lifestyle, before the stomach cramps started preventing me from going out at night/ after eating. I've also read a lot of things about surgery and I'm quite scared of the idea of having my entire colon removed. I would love to here if my experience is similar to anyone else's who has had the disease for longer and could tell me what i might expect further down the road.
Cheer,
Tom
I was just wondering if people could tell me where I stand in terms of severeness of UC. I lead a very active lifestyle, before the stomach cramps started preventing me from going out at night/ after eating. I've also read a lot of things about surgery and I'm quite scared of the idea of having my entire colon removed. I would love to here if my experience is similar to anyone else's who has had the disease for longer and could tell me what i might expect further down the road.
Cheer,
Tom