Please let your mother know that getting the feeding tube prior to starting treatment or during the first two weeks of treatment is standard procedure at many cancer centers. It will be too hard to put in a tube later on when the psatient is suffering from dehydration, mouth and throat pain. It is something that may help, like the mouth guard. My husband was so glad he had the tube when during week three he could not even swallow a sip of coffee, let alone the 2500 cc of water a day. If she doesn’t need it, then it will be out as soon as the doctors decide that she is eating well. If she needs it, it’s already there. I hope this helps her come to terms with it.


Gloria
She stood in the storm, and when the wind did not blow her way, she adjusted her sails... Elizabeth Edwards

Wife to John,dx 10/2012, BOT, HPV+, T3N2MO, RAD 70 gy,Cisplatinx2 , PEG in Dec 6, 2012, dx dvt in both legs after second chemo session, Apr 03/13 NED, July 2013 met to lungs, Phase 1 immunotherapy trial Jan 18/14 to July/14. Taxol/carboplatin July/14. Esophagus re-opened Oct 14. PEG out April 8, 2015. Phase 2 trial of Selinexor April to July 2015. At peace Jan 15, 2016.