Hello all, I'll keep this brief, just hoping someone might be able to set my mind at ease!
Basically I ended up in hospital recently, had diarrhoea for 6 weeks and had very bad joint pain primarily in my knees and elbows. They've done a biopsy and, although I'm still awaiting results, they think it's certain to be Crohn's disease.
Whilst in hospital I was on injection steroids and within a day the joint pain subsided. When they discharged me I've been put on prednisolone and mesalazine. I've been out for 5 days now and I've noticed the joint pain returning, on top of that I've still got the diarrhoea and basically I feel like I'm not getting any better!
Couple of queries, does it normally take a while for the medicines to start working? I'm not sure if I'm just being impatient or if the lack of progress suggests I should be going straight back to the doctors. Also, I've been googling (I know, not always advisable!) and everything I've seen suggests that mesalazine is good for treating UC but is of little to no benefit if you've got Crohn's disease. Does anyone with Crohn's have a good experience of mesalazine or should I be asking why they've got me on it and asking if there are alternatives? Really don't want to end up back in the hospital but since leaving, going to oral steroids and mesalazine I just feel that all the problems are coming back and I'm a bit anxious!
Thanks for taking the time to read this!
Basically I ended up in hospital recently, had diarrhoea for 6 weeks and had very bad joint pain primarily in my knees and elbows. They've done a biopsy and, although I'm still awaiting results, they think it's certain to be Crohn's disease.
Whilst in hospital I was on injection steroids and within a day the joint pain subsided. When they discharged me I've been put on prednisolone and mesalazine. I've been out for 5 days now and I've noticed the joint pain returning, on top of that I've still got the diarrhoea and basically I feel like I'm not getting any better!
Couple of queries, does it normally take a while for the medicines to start working? I'm not sure if I'm just being impatient or if the lack of progress suggests I should be going straight back to the doctors. Also, I've been googling (I know, not always advisable!) and everything I've seen suggests that mesalazine is good for treating UC but is of little to no benefit if you've got Crohn's disease. Does anyone with Crohn's have a good experience of mesalazine or should I be asking why they've got me on it and asking if there are alternatives? Really don't want to end up back in the hospital but since leaving, going to oral steroids and mesalazine I just feel that all the problems are coming back and I'm a bit anxious!
Thanks for taking the time to read this!