The more knowledgeable members of the forum might know, but I am wondering if the radiation field and the amount of radiation given are factors in why some patients manage to go through TX without a PEG and others needed it from around the mid-point of TX. John got his PEG the third week of treatment and had to use it starting the fourth week because he could not even manage four sips of coffee. Yet, another gentleman we met at the hospital who was being treated at the same time managed to continue eating till the last day of treatment -- he even had a turkey dinner for Christmas. Irrespective, I believe that determination and whether you have someone to keep on pushing you to eat and drink during treatment are important. During treatment, there are so many other things that need attention that it is easy to "just skip a meal." Cancer is a battle with many fronts, you might need to think about which fronts you want to focus your energy on.


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.