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
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