I’m sorry that your dad’s doctor was not more sensitive in discussing his treatment. Personally, I always remind myself that the prognosis is at best an educated guess and many things may happen that may change it. Like my husband’s RO said one time, if we were told that 2 out of 10 patients had problems with a particular treatment, before getting upset, we needed to remember that 8 out of 10 patients did not get a problem. I’m not entirely sure what your doctor really meant by 30% of patients are still around after 2 years, etc. What was she saying about the other 70%?
Maybe you could further explore the possibility of getting your dad another kind of chemo (immunotherapy is a kind of Chemo) or the chance of his being accepted for a clinical trial. Keep talking to the doctors and express your dad’s willingness to continue with treatment. What you can do now for your dad is to advocate for him and get him the kinds of help that he needs.
Last edited by gmcraft; 05-18-2019 05:28 AM.
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.