OP      Senior Member (100+ posts)    Joined:  Jun 2009  Posts: 138  |    Thanks for your responses.  I suppose I am trying to eat spicy stuff too soon, but Mexican food is my favorite - lol.
  Margaret, it looks like the same thing happened to your PEG as mine.  Mine was hurting and no one would listen at all and they finally did a scan and found it was out of the stomach in the abdominal wall.  They put a G-tube in then instead of another PEG tube.  That ended up being the worst part of treatment at the time, but post-treatment is becoming a real pain now.  
  I have not checked on the massages yet but maybe I will now that you recommend them.        
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
  |