During my husband's pre-treatment workups, our hematology oncologist mentioned that 75-80 percent of his patients require a feeding tube after 4-5 weeks, and that his preferred method is a naso-gastric tube. He feels it keeps the esophagus open and has better results than a PEG. Of course, this bothered my husband, although, personally, I don't care if he has tubes in every orifice if it facilitates his recovery. Has anyone had experience with the naso tube versus the PEG tube and any insights as to how easy or difficult it is to use? Ken feels that he will be able to get by without one since after his tonsillectomy, despite considerable pain, he was able to gain ten pounds in three weeks in preparation for the upcoming treatment. I'm not so sure, so would like any advice anyone can offer. Thanks everyone, this board is so helpful!


Sherry (Dolores is the name of my cat) Wife to Ken, starting chemo/radiation 10/25/04. Stage IV SCC of right tonsil, T2,N2A,MO