Guest guest Posted July 27, 2004 Report Share Posted July 27, 2004 I had mine for a couple of months. The big thing with the tube is they tend to sometimes get infected, and in my case, sepsis, which almost killed me, forget about what the wipple did to me...... good luck R > > > Hi all, > > Went back to Indiana University to see Dr. Fogel yesterday and he wants to do another EUS with possible stenting. He also wants to see if he can find any scar tissue or anything else that might suggest why I have been in the hospital so much lately. He also mentioned highly that I have a feeding tube put in because I cannot each hardly at all. Who knows about this. Who has had one. What is it like. Can you eat anything by mouth? He wants to put it so that it will bypass the pancreas so the pancreas doesn't have to work at all and this should help to keep me out of the hospital when I do get a big attack. > > I would appreciate anything anyone has to say about this. I don't know anything about it. > > Please advise. > > Thanks. > > T. (ohio) > > > > ------------------------------------------------------------------- ------- > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2004 Report Share Posted July 27, 2004 One more thing, don't let them put in a peg......very painfull!!!!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 28, 2004 Report Share Posted July 28, 2004 I had a failed Whipple procedure in Feb. of this year. I woke up post op with a J-tube which basically goes into the upper intestine. It worked fine while I was hospitalized. When I went home I started the gradual return to real food routine and that went well. We decided to leave the tube in for a month with daily flushing and general wound care at the site. We wern't sure how well I was gonna make it at home and wanted to have it in place in case I was re- admitted. Before the month was up I was admitted to my local hospital. They chose to put me on TPN instead of using the J tube. To make a long story short, it had to be pulled out due to both site infection and intestinal infection and blockage. I wouldn't have another one for any reason. Most of my good arm veins are pretty well shot from all the use over the past 4+ years so, I'd opt for a central line (with all it's inherent risks) or TPN in whatever vein they can find that works. More questions?...just ask !! Best of Luck, Knox Northern Ca. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 8, 2004 Report Share Posted August 8, 2004 Leanne, after dropping 90 pounds this past year, we're getting mobelized for a semi permenent, at least long term look at maintaining nutrition... I have had the NJ tubes many times as well as picks with TPN, but this is the first time I heard the buzzword Jtube... Could you tell me more about it.. Is this the same as the abdominal peg? Thanx, ricki Quote Link to comment Share on other sites More sharing options...
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