- Joined
- Nov 14, 2011
- Messages
- 974
budesonide/entocort
I am slightly confused!
Yes I know nothing new there then! :wink:
I have always been told I had UC. There was some doubt when i had an mri last August as it showed inflammation and scarring in my terminal ileum.
Since my sub total'ccolectomy aand temp stoma I have beebeen having aa worsening flare in my rectal stump. Had used pentasa/mesalazîne suppositories then onto cortifoam(butt facials) enemas. Both were no good and had no effect on my flare.
Have been having telephone consultations with my ibd nurse and she has prescribed me cipro antibiotics and entocort/budesonide.
Both of these are predominantly used in the treatment of crohns not uc.
Has anyone had any positive experiences with either.
Also anyone with UC been on these before.
I am wondering if she has given me these as a last ditch attempt to get this awful flare under control or because she thinks i have Crohns.
I have asked if I have crohns but i get the answer of - when we did the biopsies, after my aazathioprine, Mercaptopurine and remicade treatments, they all came back as showing no active disease.
This, to me, sounds like they could not find anything at that time. Not that i don't have crohns as well as uc.
Bear in mind that when they did tthe biopsies looking for Crohns my UC didn't show up either!
Sorry for the long post got a bit carried away!
I am slightly confused!
Yes I know nothing new there then! :wink:
I have always been told I had UC. There was some doubt when i had an mri last August as it showed inflammation and scarring in my terminal ileum.
Since my sub total'ccolectomy aand temp stoma I have beebeen having aa worsening flare in my rectal stump. Had used pentasa/mesalazîne suppositories then onto cortifoam(butt facials) enemas. Both were no good and had no effect on my flare.
Have been having telephone consultations with my ibd nurse and she has prescribed me cipro antibiotics and entocort/budesonide.
Both of these are predominantly used in the treatment of crohns not uc.
Has anyone had any positive experiences with either.
Also anyone with UC been on these before.
I am wondering if she has given me these as a last ditch attempt to get this awful flare under control or because she thinks i have Crohns.
I have asked if I have crohns but i get the answer of - when we did the biopsies, after my aazathioprine, Mercaptopurine and remicade treatments, they all came back as showing no active disease.
This, to me, sounds like they could not find anything at that time. Not that i don't have crohns as well as uc.
Bear in mind that when they did tthe biopsies looking for Crohns my UC didn't show up either!
Sorry for the long post got a bit carried away!