Hi guys, I'm recently diagnosed with UC and I've had my first flare and it was awful. However, as bad as things were - it doesnt seem as bad as what some people describe.
At the worst of it i had -
pain when eating/drinking - on the very worst day i even had pain from laughing or bending down/sitting up
I was going 4/5 times a day - all loose/liquid and regular bleeding.
It got to the point where i expected to see blood every time and that i forgot the last time i had a solid stool
I was put on prednisolone and 4 weeks into it, I finally started getting solid poos!!! hooray!
At first, the stools were solid but there was still a bit of blood for the first few days, but it was different, blood was attatched to bits of the stool rather than coming out in a horrible dark wet clump (gross, sorry)
A few days later and that disappeared too. I went from 3 poos a day, to slowly 2 poos a day and for the last 2 weeks i've been on 1 poo a day.
I'm finally off the steroids as of Tuesday, i'm now on 3 mesalamine pills a day.
I have one stool a day that tends to be mostly type 4 - starts as smooth snakes, but normally goes into little small bits with clear cut edges at the end (type 5?) - sometimes the water goes a tiny bit cloudy at the end of a bowel movement which concerns me but I don't know if im overthinking the cloudyness?
My doctor said that I should only be concerned about two things -
FREQUENCY
BLEEDING
well, i'm going once a day and haven't seen bloody in 2 weeks, so i imagine thats a good sign? Should I just stop worrying about stool shape/size and the cloudiness of the water and get on with my life?