Hello everyone,
Just thought I would introduce myself. I am 23 and got diagnosed last year (after a years of stomach problems and misdiagnosis) during a particularly bad flare up. I was put on steroids for 8 weeks which stopped the stomach pains. After that I was put on Azithorpine and remain on them now (150mg a day). Since then the flare ups have been less frequent and when the do appear the are usually only a few days. Compared to the weeks a used to go through this is a welcome relief. However, my day to day toilet habits have not improved. Everyday I make frequent trips to the toilet often lasting 20-40mins sometimes more. It is not always diarrhoea, in fact it is often constipation. I know this is an unusual crohns symptom but just wondered if anyone else suffers this? I always have blood in my stool as well.
I would also like to say that I am getting surgery at the start of next year and would like to know peoples experiences.
My last question was about the lofflex diet. I am currently suffering a flare up and have decided to start this diet despite my doctor insisting that diet has nothing to do with crohns. I was wondering if anyone managed to get on the liquid diet before this and if so how they managed to convince their doctor to give it a go?
Cheers
Just thought I would introduce myself. I am 23 and got diagnosed last year (after a years of stomach problems and misdiagnosis) during a particularly bad flare up. I was put on steroids for 8 weeks which stopped the stomach pains. After that I was put on Azithorpine and remain on them now (150mg a day). Since then the flare ups have been less frequent and when the do appear the are usually only a few days. Compared to the weeks a used to go through this is a welcome relief. However, my day to day toilet habits have not improved. Everyday I make frequent trips to the toilet often lasting 20-40mins sometimes more. It is not always diarrhoea, in fact it is often constipation. I know this is an unusual crohns symptom but just wondered if anyone else suffers this? I always have blood in my stool as well.
I would also like to say that I am getting surgery at the start of next year and would like to know peoples experiences.
My last question was about the lofflex diet. I am currently suffering a flare up and have decided to start this diet despite my doctor insisting that diet has nothing to do with crohns. I was wondering if anyone managed to get on the liquid diet before this and if so how they managed to convince their doctor to give it a go?
Cheers