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

 

Parents
  • Hi

    I just wanted to thank everyone involved in this thread, as reading it has been incredibly helpful over the last few weeks.

    My husband had a swelling on his neck diagnosed as cancerous at the start of this month (April 2019).  It was a shock: he's never smoked, rarely drinks, cycles regularly, eats sensibly and is in good health - or so we believed.  Since then he's undergone a CT scan and biopsy which have confirmed the tumour as being at the base of his tongue and HPV16+.  He hasn't had his tonsils removed, as the sugeon doing the biopsy/panendoscopy thought they looked OK, but going by the scan the consultant thinks one has been affected, as well as some lymph nodes.  He gets assessed by the dental team tomorrow and has an MRI booked for the end of this month, plus whatever other appointments are yet to be arranged, with chemoradiotherapy due to start in about 4 weeks.

    The last couple of weeks have been stressful (to say the least!), but this - and a couple of other similar threads - have been incredibly useful, as have the wonderful blogs by Ian and Hazel.  Having an insight into the treatments and their side effects meant that we felt quite well informed about what lies ahead even before speaking to the hospital consultants, and instead of everything being a blur, we were able to take in what was said and manage to ask some sensible questions.  Without all of you generously sharing your experiences it would have been a very different story.

    Because of that, I wanted to let people know how important this thread has been for us - and that all your tips for coping with the treatment etc have been gratefully noted!  It's not a good situation to find ourselves in, but we feel pretty positive that we'll come out the other side in one piece.

    I hope everyone who has posted, or who might be reading this, is doing well and continues to do so. 

    Thanks again, and best wishes to you all

  • Have to echo this, prepared me so well, a Godsend.

  • lol Hazel - get a spell checker

    nice to see your back safe n sound and hope you brought the weather back with you.

    ian

  • Great to hear you are in good form Hazel, your posts are hilarious as well as informative

    Dave

  • Hi all,

    Just for info in case any unaware and wondering re frequency of check ups post treatment.

    At my check up today with consultant - (just a little swelling still back throat but its fine)
    They feel neck, have a look around mouth and I got scope via nose. and ask you how you are feeling/getting on. Appointment lasted about 15 mins I guess.

    Anyhoo on checks ups I was told ( assume same for others )

    Check up every month for first year after treatment

    Year 2 to 4 checked every 3 months

    Year 5 every 6 months

    Hopefully then all still clear and in remission and no further checks.

    Onwards & Upwards
    Ian

  • Hi Ian brought the rain back with me ! Has brill crossing was quite worried as last May I was in a state in the boat , obv didn’t know at the time that it was the cancer upsetting my equilibrium! Spelt that without a spell checker. Lol ! My brain works too fast for  I pads keyboards that my excuse or other excuse I missed the week at school when we did spelling !!! Plus no one would have anything to laugh at if I didn’t do  typos  i have  proof read the above and maybe for once perfecto ! Grammatically rubbish probably. !

    love being away but  like Insaybto John it’s a fantasy life we lead over there back home it’s the real world and wouldn’t want to be there permanently.

    cathcing uo with game of thrones and tour de yorkshire

    keep in touch buddy onwards and upwards.

    H x 

  • Hi Ian just shows how things are different in different areas .

    i haven’t had a scope up this diagnosis day mine don’t believe in doing them after that 

    year one every 6 weeks ( I negotiated holidays ) saying you told me to go and live my life so that she what I am doing with provision I would fly home immediately if I felt anything wrong .

    year 2 every 2 months 

    year 3-4 every 3 months

    year 5 every 6 months.

    My check ups are flashlight down into mouth whilst he holds my tongue with a piece of gauze,that makes you feel sick.Good feel of neck area and general conversation of how I am feeling eating etc .

    Maybe it’s coz us Yorkshire birds are tough !!!!!

    Hope this helps people as like we say we are all different with the same diagnosis.

     

    h x

  • HinDave how are you doing glad I make your day !!!! Back in good old Blighty .wwont ask what the boys are doing but a few of them need their p 45 s pretty dam quick without big payoffs . 

    Thursday night europa leagues not going to do us any favours next season either.

     

    keep in touch superman 

     

    H xx

  • Im good thanks Hazel, still dry mouth problems especially when excercising playing football etc, I get bouts of fatigue too but overall good thanks, I have a check up mid June then every 2 months (I think) we are off to Gran Canaria at the weekend first holiday since last September when all this started, really ready for it :)

     

    Dave

  • Hi Dave enjoy the holiday Julie amd yiu will be ready for it , justbremember factor 50 for the neck and mix a bit of fake tan in with it yiu will be fine. Plenty if water for flight unfortunately yiu will have to pay WH Smith a arm and a leg airside for it but I found flying dries me uo before and does more now .enjoy have a brill time

     

    h x ps go into mercadona supermarket whilst away get Trident dental chewing gum with xylitol in it ut really helps I’ve brought loads back 

     

    h x

  • Thanks Hazel good points I expect aircraft cabins can cause us to feel dehydrated, noted thanks.

     

    Dave

  • Hi Dave i flew from Tenerife to Edinburgh and back last week, took 1.5 litres with me each way, with that and gum i was fine,no other issues, but booked aisle seat both ways for loo and to stand plenty. All worked great, bit dry nose. Glad you are doing well.

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