Throat cancer

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Hi all, so glad I found this forum and I hope it helps me and hopefully I help others. 

I've had a horrible battle with Throat Cancer for 3 years now, 36 Radiotherapy, 2out of 3 chemo( was too I'll for the 3rd), it came back after 8 months so I had 12 and a half hours surgery to remove a tumour and part of my tongue. I'm in Remission now and so so grateful. 

I'm left with silent aspiration, I can't swallow safely as food can go in my lung, I've had Pneumonia 6 times in 18 months by trying to eat Frowning2. I struggling around this but I have exercises to do and a slim chance of eating pureed food one day. I hope n pray!

Anyone with a similar issue? Any support would be much much appreciated, I live alone. Thanks so much x

  • Hi Lonewolf.

    Welcome to the community but so sorry to find you here with such awful side effects. I can't speak for myself as I've made a fairly uneventful recovery but there are members here who are tube fed permanently and cope very well so don't despair if you find that there is no improvement. Risking pneumonia every time you eat seems pretty awful to me.

    One of our other Champs has a permanent PEG. I'm sure he'll be along later with some wise words.

    Best wishes

    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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  • Good evening Lonewolf, sorry you are going through it all again, i know the feeling very well as i had it 3 times within three years, thankfully they stopped and cured it on the last operation back in 2010. I cannot speak as my voice box was removed in the last operation also im PEG dependent on food intake but can swallow thin liquids so its not all bad. My problem is not because of food going down my lung it's just my swallowing is not good enough plus my tongue was also operated on in my first operation which as you know affects swallowing a lot. I did try all the exercises etc but unfortunately, they did not work so i have now settled to PEG feeding which is now part of my new life. Hopefully, the exercises work for you and you will be able to swallow pureed food as its better than PEG  feeding and tastier Slight smile. Please feel free to click on my name and it will take you to my profile where i have written about my dealings with head and neck cancer. Wishing you all the best and hope things improve for you, take care.

                                                                                                  Chris 

    Its sometimes not easy but its worth it ! 

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  • Hi Lonewolf welcome from me. I can’t add to Dani and Chris s posts but feel free to rant in here we’re all here for each other. 
    Hazelx

    Hazel aka RadioactiveRaz 

    My blog is www.radioactiveraz.wordpress.com  HPV 16+ tonsil cancer Now  6 years  post treatment. 35 radiotherapy 2 chemo T2N2NM.Happily getting on with living always happy to help

    2 videos I’ve been involved with raising awareness of HNC and HPV cancers 

    https://www.instagram.com/merckhealthcare/reel/DBs8Y0niJ8N/

  • Thank you Dani so much for your reply, means alot. I'm feeling a bit more positive now, blessings, Wayne.

  • Thanks Chris, your post has helped me, I'm in a more positive place today. See my nutritionist Thursday and I can have soups as long as they are smooth. Those that aren't I just blitz with the food blender.

    I admire you Chris and you have done so well to manage, God bless you and thanks again,  Wayne.