New here Tongue Cancer

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Hi just wanted to say hello

I had my left tongue dissection went home after 11 days, found out Tuesday (12 days being home) that I do have to have radiotherapy & chemo. 

Quite daunted by the prospect but hoping some have advice on dealing with side effects, what your experiences were. 

thanks 

Teri 

  • Dani 

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

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  • HellovTeri

    i’m Nige, good to meet you, wish it was better circumstances. 
    I had chemo and Radiotherapy, finished mine on the 10th January.

    i’ I’m happy to give you my experiences and things I had with the side effects.

    with chemo, I felt my noticeable side effect was tiredness and fatigue. I look after dogs and was very active out with them , for the first Fred weeks that was ok but after the 3rd week i did notice I hadn’t the energy so had to really cut back.

    as regards the Radiotherapy, I quite embraced the mask, in fact I found it a comfort and virtually dropped off asleep whilst having the treatment.

    re the side effects, they were gradual over time - firstly the loss of taste, that eas gradual, but things tasting changed - followed by the dryness of the mouth, slow but steady dryness. I also found my appetite was dropping but in two ways , wanting eat and the trying to eat. 
    taking fluids is so so important , and having the protein drinks were the way for me. In fact today, 4 months after treatment finished , I still take the protein drinks - finding the ones that were ok to the taste was also key. To make them easier to swallow, I missed them with full fat milk. As my taste buds are slow to return, eating is still a real problem so perseverance is key.

    while eating I do tend to have drinks available with me, , swallowing solids are made easier that way.

    if there is anything I can help you with in any way, please ask - always here to help !

    all the best

     ige