Radiotherapy for Throat Cancer

Hello all,

I have posted my little story on introduce yourself and basically I have been diagnosed with Stage 1 Throat cancer.

The prognosis is hopeful and I remain cheerful and positive. Its taken a while for the actual treatment to start so glad to get on with it at last.

I started my first day of radiotherpy today and have 29 more treatments to go over 6 week period.
I have made a little computer programme that logs my side effects and summarises episodes of each heading and I plan on keeping a daily log of how things went/ how I feel ( good and bad ) and map out my journey. I find it therapuetic.

I will share periodically in the hope that even if it helps one person as well as myself  it will be worthwhile.

So day 1 was fine and I dont really feel any difference or notice anything.
One small point is that the mask made was slightly harder than when it was first made as it has set little harder over the weeks and was a little more moveable on the day made.
Took about 10 mins for actual radiotherpay treatment itself.
Drove home fine.

Meet with advanced practioner nurse every Thurs to discuss progress.
Aware might be a little different along the way but all good after day 1.

 

kind regards

Ian

 

  • Hi all 

    My hubby has now got a date for the procedure to stretch his gullet. First week of July. He's so looking forward/not looking forward to it.
    Hoping it will sort out his ability to swallow as he can't even swallow a sip of water at the moment. Obs being peg fed. He's so fed up with that!! 
    Love to all

    Chrissy X 

  • Hi Davy,

    Yup this is an old thread now but has been going since 2018 and so many positive contributions from so many and we have all helped one another along the way.

    It is challenging though treatment & recovery but you get there in the end with the light at the end of the tunnel and you will see so many positive stories and outcomes on here. I was told from the get go by my consultant that it would be challenging but also told one of the highest rates of success for cure and that helped keep me posiive along the way.

    I wish you well on your journey and we are all here for you if you need any help at all.
    Ive also posted my blog which may help as well.

    radiotherapythroat.home.blog

     

    regards
    Ian

  • Hi there Chrissy,

    I'm so pleased he's got a date for the procedure - it must be so tough for both of you continuing with the peg feed. Obviously never fun to undergo another procedure - but hopefully that first cuppa will be so worth the wait! Take care. Love to you both x

  • Thank you so much Weaselbear 

    xx

  • Hi Davy,

    So sorry to hear about your diagnosis. I've supported my partner through tonsil cancer treatment. Hazels and Ian's blogs were incredibly helpful reading! Everyone on this forum is here for you whenever you need support, or have a weird question, or just to vent. 

    The treatment is tough but has really high success rates. My partner is 7 months post treatment and back playing football, mountain hiking and eating pizza! Good luck and we're all rooting for you. X

  • Hi Chrissy fingers n toes x that all goes well. Sending hugs and please keep in touch. 
    Hazel xx

  • Hi anchor

    Got my specialist meeting on Wednesday when I get my treatment plan and what will be what, I can't say I'm not nervous as I am terrified as he will also have the results from my CT scan too but hey 4 days to go

  • Hi weasel 

    Thanks for your kind words and I hope my treatment is successful like your partner I do worry about my wife at times it is hard for her too but I try and show her I'm OK and not worried as I don't want to add more pressure on her. My next post will be Wednesday after specialist meeting. Thanks to all good to talk. 

  • Hi Davy

    Totally understand and its tough time waiting for results but as you say Wed will soon be here and knowing your treatment plan is the first step forward.
    Treatment nowadays is so advanced and technology available now is amazing.

    It is tough on partners as well and I have a special shout out for all partners in my blog as they are so important for support before,during and after treatment. 
    All the focus is on the patient but my support team was particularily helpful with my partner and it was  at times, easier to relay information when both at appointments.

    We are all rooting for you and all here if you need any help,support or advice.
    Let us know how you get on Wednesday and this is the start of your recovery when you know what treatment plan is.

    kind regards
    ian


     

  • Hi Chrissy

    sending my best wishes to you both and it can be really tough during and after treatment so hang in there and hope once procedure carried out, it all becomes a little more comfortable and bearable with swallowing and able to sip and drink water.
     

    kind regards

    Ian