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 Laura,

    Thank you and sorry Micks side effects ramped up. Although temporary it doesnt make it any easier at the time and wish him well and I hope you are coping and doing ok as well.

    Hope Mick has a good week and keep us posted.

    Ian

  • Hi Ian. Good luck for tomorrow,I am sure all will be absolutely fine,let us know when results  are in . I had a 10 day wait hopefully yours will be quicker 

     

    hazel who is  getting ready for road trip ,taking 96 ensures with us in then car just in case. Lol bush tucker trials on the beach ! 

  • Great stuff Hazel and even more reassuring.

    Now go and enjoy your trip

     

    ps: agree re gas bill. my heating been on constant as more or less in house all time so expecting a steep one as well.Need to keep warm tho.

    ian

  • Hi Ian will do, yep not looking forward to direct debits increase  ouch I turn it up,John turns it down! 

    Forgot tomsay although no camera consultant put a gauze on my tongue so he could pull it a bit without his fingers slipping omg I nearly gagged then he wanted me tomsay eeeeeee not a chance u hold your tongue out n try and say it it’s impossible !!!! Pleased no camera though

    onward and upward , hope your heatwave helps with heating over weekend

     

    keep in touch let us know ASAP when u get results ,will keep everything crossed 

     

    h 

     

  • Hi Hazel

    wow with you saying eeeee, that has just trigged in my mind I had an appointment with Speech and Language. I do  - this Monday at 12.00 noon !!
    Never had the gauze before and doesnt sound too comfortable so maybe something else I have to look forward to.

    I completely forgot all about appoinetment and its only thanks to you that I would not have shown up so thank you.
    To be honest, I have long weekend booked for annual leave and no work etc and may well postpone until after I get results.Seems an ever ending list of appointment schedules.

    We can also maybe start a gofundmegasbill# and split it between us lol

    and yup Onwards and Upwards for us all and will defo let you know results no matter what outcome.

    ian 

  • Thank you everyone for your updates, they're always interesting to read. My partner finished his radiotherapy last Friday. He still eats very little, this used to be due to the vile taste, but now because of the pain. But I'm really impressed that he's only taking 4 paracetamol a day, nothing else. He's having 3-4 ensures a day into his PEG tube. He's still very inactive and isn't talking much, and his spirits have been low for most of the treatment (chemo was awful for him, they stopped this after week 4). Next week our girls go back to school (primary school age). Hopefully the weather is nice. I'll continue collecting them from school but I'll suggest to my partner that he leaves about 20 min after me and to meet us on our way back, I'm not even sure he can walk all the way to school now, he looks so frail (it's a brisk 10 minute walk). He used to do most school runs and my girls are really missing those. They're looking forward to him playing again (Lego, taking them to park etc). I'm looking forward to being able to have a proper conversation. It's like having a stranger in the house and my girls have found it very hard (he was always a very hands-on dad who did loads around the house!).

    Keep on posting!! 

  • Hi Louisabel.

    I was where you are when my husband had his treatment. You will find patience you never knew you had. As you will have read the treatment goes on long after completion.

    My hubby sat in front of a tv but could not tell you what programme was on. I would say everyone is different but in his case it was about a year before he got back to his old self.

    Do you think his pain is properly addressed with 4x paracetamol if pain is affecting his ability to eat?

    This is great place to find hints and advice. There is always folks come along if you need a bit of a chat or whatever.

     

    Kind regards xx

  • Hi Louisabel,
    On one hand its good that radiotherapy is now over but I'm afraid in most cases this is where the side effects are most challenging while on recovery phase.
    I totally agree with Clara for rasing the fact only on 4 paracetamol. It's not a case of being impressed but making sure that appropriate painkillers are taken to control the pain. As he cant eat because of the pain I would suggest he is not getting the painkillers required into his system.
    Painkillers are there for a reason and no one should be in pain, with or without eating when there is a solution to control it, but only my opinion.
    I would really advise you to speak to his support team/GP and let them know what he is taking and I'm sure they will advise accordingly, especially as you desribe such pain.(It was at this stage I needed morphine the most).

    On exercise we are all different and while there are a few who have managed to exercise quite soon after radiotherapy just stopped,some, like myself, did not have the energy to go out walking much.
    We are all different and we all need our own personal recovery time no matter how long it takes.My consultant told me it can potentially take a year or so for bodies to fully recover and get back to way they were before treatment,

    Hope this helps and blogs from myself and Hazel,cover post treatment / medications etc at various stages and based on our personal experiences.

    Link my blog again is below and also contnis a link to Hazel's

    radiotherapythroat.home.blog

    regards
    ian

     

  • Hi

    My partner was the same both with the taste but also the pain was so intense and unbearable so didnt eat for about 6weeks and just had 8 bottles into his NG tube ( he lost that much weight his dietician advised she wanted him in hospital and he stayed in for two weeks after his radio finished. 

    I agree about the medication maybe ask about morphine (mine was on patches for months along with oral morphine and paracetamol) .

    He is still very tired but managing walks and little trips out but this week he has done nothing due to the fact he was out and about last week.  So he is just listening to his body and also everyone is saying about 12 to 18 months before he will be back to his normal sefl.

  • Hi Louisa bel 4 paracetamol is nit sought atbthis stage please see someone about pain relief the clue is in the name pain killers inwas in oramorph and 30 mg co codomol for 5 months almost inweaned my self gradually offvthem with no side effects please please see someone 

    detail s in my blog www.radioactiveraz.wordpress.com

     

    h 

  • Hi Louisabel

    I so feel for you and your girls - its such a difficult time for the whole family. My hubby was diagnosed in Dec 2015 and following chemotherapy/ radiotherapy and a neck dissection he has been in remission and cancer free since July 2016. I just wanted to say that how you are feeling is completely normal - its difficult to watch your partner go through such arduous treatment and be powerless to help. However the fatigue and disinterest in life will pass. I really think its the brains way of coping with the treatment- to shut down to anything other than just the basic functions - however as the effects of the radiation leave his body slowly but surely your hubby will reappear as if from hibernation .Hang in there - stay strong - youve got him this far and you will make it through. 

    If you need to chat then feel free to send me a friend request and keep letting us know how you’re getting on.

    best wishes

    Emma aka Newlymarried 

  • Hi Louisabel,

    Just a quick note to ask if you managed to get hubbys pain under control as been a few days since posted and hope all much better.

    Again to reiterate to speak with support team as I'm sure they would re iterate advice given that a few of us have personally been through at that stage. Perhaps also maybe mention the few ensures and nothing else he is taking although I totally understand how difficult appetite is on recovery.
    Again both Hazel and myself's blogs detail issues in more detail such as pain medication and also appetite and exercise.
    Appetite and fuel intake is a hard and prolonged one for many of us.

    As Graeme asked to put handy links on when posting about blog, I have listed link below again should you wish to read  and Hazel's link in there as well.
    Really hope a resolution found but please feel free to ask away if I can help further in any way.

    radiotherapythroat.home.blog

    kind regards
    ian

    note : Graeme, I hope you dont mind but I've incorporated some of your useful tips you posted into my blog as well as I'm sure will help others.

Reply
  • Hi Louisabel,

    Just a quick note to ask if you managed to get hubbys pain under control as been a few days since posted and hope all much better.

    Again to reiterate to speak with support team as I'm sure they would re iterate advice given that a few of us have personally been through at that stage. Perhaps also maybe mention the few ensures and nothing else he is taking although I totally understand how difficult appetite is on recovery.
    Again both Hazel and myself's blogs detail issues in more detail such as pain medication and also appetite and exercise.
    Appetite and fuel intake is a hard and prolonged one for many of us.

    As Graeme asked to put handy links on when posting about blog, I have listed link below again should you wish to read  and Hazel's link in there as well.
    Really hope a resolution found but please feel free to ask away if I can help further in any way.

    radiotherapythroat.home.blog

    kind regards
    ian

    note : Graeme, I hope you dont mind but I've incorporated some of your useful tips you posted into my blog as well as I'm sure will help others.

Children
No Data