Welcome to the group though I am sorry you have to join our circle of friends,

I second Christine's suggestion to get a second opinion at a comprehensive cancer center where the doctors have seen many different cases of cancer and where they use a team approach to treatment.

Do you know how much radiation you father has had -- 12 weeks in all sounds like an awful lot. Opdivo is a new drug and it is a kind of immunotherapy where they try to marshall the body's immune system to fight the cancer. We have a couple of members who are on it/or it has been suggested to them. You can find their posts under the recurrence thread.

Ask your father to carry a spit cup. My husband had one for months and carried it with him everywhere. It was just a disposable plastic cup. Being able to spit helped to keep the amount of phlegm in his mouth to a minimum. The waterpik is very effective for cleaning out dried phlegm and keeping the mouth fresh. If you dad has the magic mouthwash, adding a capful of that to the water helps too. Use the tongue scraper attachment on the lowest setting.


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.