hi all.i have just discovered this forum whilst looking for further info on this type of cancer(just a personal interest) and I am so sorry to hear how you are all having to face this hideous cancer.i was diagnosed in 2012,with tonsil cancer and my life,and that of my family thrown into turmoil.i needed 30 rounds of radio and 3 of chemotherapy as an inpatient at the Christie,Manchester.the nausea and metallic taste from the cisplatin and 5fu chemo were very unpleasant,and I couldn't face food at all.just a fresh,clear chicken soup my mum made.the radiotherapy caused a lot of pain and by week 3 I could hardly get fluids down.i was given a nasal gastric tube and it was very difficult to get the right 'feed'as they all caused vomiting.i couldn't keep it down.I live alone but fortunately live next door to my parents so I had lots of help.everyone's experience will vary though of course there will be many similarities.getting the right pain relief is crucial.i had morphine and a wonderful paracetamol mixture which had all sorts in it.though I can't remember what exactly.it is a gruelling ordeal to have to go through.i have suffered with chronic depression since 1989 and so trying to endure the treatment was a challenge indeed.i have just made my 5year anniversary of being given the all clear so stay strong guys.i found out that this type of cancer may be caused by the human papilloma virus.i had never heard of it and was devastated.teenage girls are vaccinated now so as not to contract the virus,but not boys.i have made my son promise that he will pay to have my 6 year old grandson vaccinated when he is old enough.it costs around £350.wishing everyone good luck with their treatment.
kind regards
karen