When I was going through bladder cancer, it might be the same thing they offered me, but I cannot Myself so they decided an ilio conduit would be better as it requires no regular cathetering. I remember he referred to it as a artificial bladder, that was in 86. I don't mind the ilio conduit, it seems easier than having to be catheterized. It was considered rare for a woman to have bladder cancer in 86. They had not had very many patients that were female with bladder cancer. Craig did a study about those and later called me. Dana In a message dated 3/10/2012 8:48:19 P.M. Central Daylight Time, [email protected] writes:
I asked about this and they assure me it is not the same. I think with the conduit one still has to cath themselves. I was also told by some people it could be referred to as a Florida pouch, but they tell me that is not the same procedure. They kept referring to it as a chimney. On Sun, Feb 26, 2012 at 12:57 PM, Quadius <[email protected]_ (mailto:[email protected]) > wrote: They tell me that is the common name, although some people tell me the ileo conduit is another name, but I'm not sure. On Fri, Feb 24, 2012 at 12:01 PM, <[email protected]_ (mailto:[email protected]) > wrote: Quadius, does this procedure have any common names? Best Wishes In a message dated 2/21/2012 5:51:34 P.M. Central Standard Time, [email protected]_ (mailto:[email protected]) writes: I have been experiencing a multitude of problems over the last year and finally I had a cystoscopy done in August which showed there were no stones or any other obstructions. I had been experiencing a lot of pain from the catheter rubbing against the back of the bladder wall. I have managed to tape my suprapubic (SP) against a stat lock device that I'm using on my lower abdomen. This is working well with the pain most of the time, but I am still having problems with my catheter not draining properly at times. Repositioning the bag so that the urine has to travel up seems to help about 50% of the time, but there also seems to be those times when we have to flush with some saline in order to get it draining again. When I explain this to be urologist, who works on a multitude of quadriplegics here in Tampa and as been my urologist for the last 10 years) she informed me that I would be an ideal candidate for the ileovesicostomy. She told me that my catheter had atrophied so significantly that it was probably one of the only options left up to me. I have been procrastinating and thought I had everything resolved, but I have been experiencing a lot of problems lately. I think I'm just delaying the inevitable. Has anyone on this list have the procedure and if so would they mind telling me their experiences? I am searching through forums right now and trying to gather as much information as I can. I'm planning on scheduling another meeting with my urologist in order to allay my fears. I haven't had surgery since I have been paralyzed and I'm terribly frightened of general anesthetic. I don't want to be put back on a ventilator after spending four months of what I now think were the worst months of my life fighting to get off the ventilator. Anyway, if you can help out I really appreciated. Quadius PS please excuse any errors. Among the backup to my backup microphone and it has some static bursts into it right now. I really need to get my computer and microphones within working order again.
