Victor,

Super that you got someone to look at you.

I think regarding the chemo....you have to think about the fact that it is simply a tool to help the BIG GUN (radiation) have the greatest impact. The chemo makes the cancer cells more sensitive to radiation. I am sure those with more technical expertise will chime in on this...it seems everyone on this board has different treatment regimens.

Yes, Cis is ototoxic so be aware of hearing issues which usually shows up as ringing in the ears. So far, it doesn't seem to have damaged my Bill's hearing.

Victor, do you have a caregiver...someone that can fight these battles for you when your treatments begins to take a toll on you?? Starting about week 4 of your rads...you will not feel well and will need someone to turn to for meds, food and water. Someone will need to calculate your intake of all the above and keep it at an optimal level. I hope your have someone.

You are smart to turn to this board for answers...we will tell it like it is..and help you keep you sanity.

Deb


Deb..caregiver to husband, age 63 at diagnosis, former smoker who quit in 1997.
DIAGNOSIS: 6/26/07 SCC right tonsil/BOT T4N0M0
TREATMENT START: 8/9/07 cisplatin/taxol X 7..IMRT twice daily X 31.5.
TREATMENT END: 10/1/07
PEG OUT: 1/08
PORT OUT: 4/09
FOLLOWUP: Now only annual exams. ALL CLEAR!

Passed away 1/7/17 RIP Bill