tonsil cancer survivor 8 years

Former Member
Former Member
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hi all I had cancer on my tonsil and am now clear 8 years. I have been trying to find someone who has also had it to discuss long term side effects, but i have been unsuccessful . is there anyone who has had the same thing?

i was very fortunate as it was found quickly and it was only small and hadn't spread. i had 30 sessions of radiotherapy and am free and clear.

when i was told of the side effects of the radiotherapy ie pain ,swelling , bleeding , not being able to eat and possibly being fed through a tube i thought NO WAY. so i saw a medical herbalist and explained everything and could she do anything for me. The answer was YES she gave me some herbal tea and i had it every day. the result NO pain or swelling or bleeding. in fact i sailed through the treatment and recovery. She called it her sore throat tea and i still take it if i feel a sore throat coming on.

i was so positive about my treatment and the whole experience i wasn't going to let it get to me.

i just would like to talk to someone who has had the same cancer as me to compare notes as it were about the long term side effects. 

  • Hi Dani

    I have watched the webinar and I found it  very informative. Emma  Hallam covers so much and  communicates over so well what  it can be like for us if we are living with some of these long term after effects of our treatments. There is great advice, tips and I learnt new things too.

    Best wishes

    Nicky

  • I've found her so helpful. She's pretty good at signposting other services and helped me find information local to me. She posts some useful stuff on a well known social media platform begin ng with TW.

    One of the things that struck me was the number of people who were unaware of long term side effects. There is a lack of communication somewhere. It must lead to a lot of worry. 

    I hope you're managing OK. You've had bit of a ride...

    Dani 

    Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019

    I BLOGGED MY TREATMENT 

    Macmillan Support Line -  0808 808 00 00 7 days a week between 8am-8pm

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  • Former Member
    Former Member in reply to RadioactiveRaz

    hi Hazel i can only taste onions and melon everything else is tasteless. i cant eat most meats or fish. i can manage a fishfinger so its mainly eggs and lots of fruit and veg.  if i try and use even pepper or ginger it burns my mouth so my diet is pretty bland but when you cant taste anything it doesnt matter does it. i just think i am here and healthy and blessed

    linda

  • Hi Dani 

    I was really impressed with her whole webinar.

    Yes I totally agree with you, she is very good at  signposting to  other services too,  when these services are needed. It is so important for rehabilitation to  be  accessed after our treatments for our QOL. in mind.

    Yes it surprises me that people are unaware of  some of these potential  long term side effects. Forums and threads like this are good because we are sharing. info to help;

    I am okay thanks, taking things as they come.

    Best wishes

    Nicky