I have had my ostomy for just over a year now (I call it my buddy!). I am currently having a terrible time with my eyes right now due to the iritis, an extra-intestinal part of the Crohn's. For the first few days my doctor had me taking T3's every four hours, which barely helped my aching head never mind the awful pain in my eye and the right side of my face. Eventually I had to see the doc again because I was vomiting all night, he chose to change my meds to Demerol. The vomiting has stopped but it doesn't seem to be helping the pain and I have found what appears to be parts of the tablet in my bag about
an hour or so after taking it. This is the norm for me as everything tends to run through me quickly, but it is possible that this is also why the Demerol doesn't seem to be doing much? Demerol is quite strong right?
My mother in law, who also has Crohns and an ileostomy, takes a slow release morphine of some sort daily for her deterioration in her spine (thanks to prednisone!). She told me that the capsules came out into her bag intact when she started, so the doctor told her to break it open and crush the pellets and eat it on toast or something. He has also given her liquid morphine so gets absorbed better. Does anyone think this would help? I guess I should see the doctor and ask before I do anything like that but the three hour wait puts me off a little!? Anyway just wondering if anyone else has had these problems?
Crohn's Disease since 1993.
Colon removed March 10/2006 with possible J pouch surgery ahead?
Asthma since 1996.
Re-occuring iritis (usually 2x a year) since 2000.
Pulmonary Embollism July 2006.