My PEG tube which I told 5 doctors was just "not right" and they kept saying, "It's fine" ended up a disaster. I went to the emergency room and the did a cat scan and found it wasn't even in my stomach any more. It was in my abdominal wall. No wonder it hurt!!

Now they say they need to put a J-tube in. I am in my 5th week of radiation and still swallowing fine. I don't even want another tube put in!! Does anyone know anything about a J-Tube that goes in your intestine? I've read it can have problems too that I don't need.


BOT-SCC Partial glossectomy 7/16/09.
Stage IV, Rt ND 10/2/09.
Teeth out 11/5/09.
Port/peg in, 11/20/09.
7 wks rad & chemo, end 1/22/10
lung, colon biopsies 1/9/11 - both cancer
colon resect surg 1/10/11
Folfox + Avastin - discontinued 6/11
lung surgery 3/13/12, 5/1/12
mets to liver and bones
passed away 9/4/13