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 there,

    Many thanks Emma & Hazel for positive comments.

    Well my first week is over and touch wood - so far so good.

    In a routine now and all my appoitments are 9.00am which I prefer.

    I am literally around 8 mins from house to hospital and have a free daily car park ticket and park right outside dept.
    Have been taken on time and Wed appt was taken at 8.58 and back in car 9.15!

    Very slick operation and staff are brilliant.
    Made a large batch of home made tablet for the staff Thursday which they appreciated and seen advanced nurse practioner who advised of potential side effects to come.
    I'm sure they will but will deal with them as treatment goes on.

     

    So week 1 has been absolutely fine with no real side effects and apart from little more tired, I just have a power napo and fine again.
    Will update end week 2 and hope more of the same.

    Best wishes to all

    kind regards
    ian

  • Hi there,

    Well week 2 is now over and again so far so good.

    Little more tired and would say started to notice more mucas but that apart I have not really felt any discomfort or noticable side effects.

    Aware goinf into week 3 next and potentially when more sied effects will kick in but will have to deal with as and when they arise.
    Will post another weekly update next week , good and bad and hope helps someone in similar circumstances.
    Happy to answer any questions based on my own personal journey.

    Staff in radiotherpay are wonderful and consider it a blessing we have the wonderful NHS.
    Not always right but by and large wonderful system and people and when you consider the cost of treatments we do not have to worry about the cost or health insurance etc over and above the diagnosis.

    Kind regards to all
    ian

  • Hi this is Hazel it’s a humidifier  not a de humidifier mine was from Amazon. It was a cool mist  around a£35 I used it every night.  What it does is make the air moist the opppsute if a de humidifier if that makes sense.
    The sticky  mucus unfortunately it is a major side effect of treatment. You can try and clear your mouth out without a flat Diet Coke. If you can tolerate it soda water that does help later  treatment mine was so bad that I was prescribed carbucysteine to thin the mucus down later the mucus goes often replaced with dry mouth  

    well done week 2 in you sound on track. Happy to hell

    if I can 

    Hazel 

  • My nephew is almost 12 months post tonsil and lymph node cancer. Doing well but still has dry mouth. During radiotherapy bought a steamer found useful.

    My husband now 7 months post radiotherapy for back of tongue and lymph node cancer. He also has no saliva. The heavy mucus stage has gone. Eating ok can't tolerate spicy food. Has to always have water available.  Uses Biotene mouthwash prescribed and bought Xylamelt tablets from Amazon as our hospital does not prescribe.

    My husband was pronounced clear at his follow up in April so good luck.

  • Iv just had my 5 years clear appointment, they said come back in a year if you want so agreed to that. Dry mouth is my only complaint really which is worse in the night or when exercising, something i`ll have to live with. 

  • How donyiu cope with it as I totally struggle with it?

  • Thank you so much Hazel, really helpful and I’ve bought a humidifier and it arrived yesterday (have yet to set it up but will do it today). I’ll see about getting some soda water in too; anything is worth a try! Thanks again for your support :-)

  • Its just something Iv accepted all the things that get recommended are short term relief 

  • My husband found pomegranate juice helpful especially for mucus. We had to buy on line but if you've got afro Caribbean grocery shop near you should be able to get there

  • After my chemo and radiotherapy I have been unable to shave as it rips my skin right off.

    During chemo I lost all my hair.

    I used to be blonde but my hair has started to grow back in brown with a hint of ginger. I really want to dye it to blonde but I am scared incase  I take some kind of reaction like shaving did.

    Does anyone have any advice or have suffered the same when doing something as simple as shaving your legs?

  • Hi Dave  5 years wow where does time go. We’re still going to apartment in Spain one life just living it. Are you still a Greece fan ? I’m 6 years this month. Fingers x we play better this year wonder how long they will give Ten Haag ?

    take care hugs Hazel. 

  • Hi I didn’t loose my hair it went quite thin. I have highlights but didn’t do any5hung with it until I reached the 6 month stage. I’ve had no reaction when shaving legs so sorry can’t help. I’ll have a scout round if I find anything I’ll let yiu know. Hazel xx

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