Treatment without tube

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Hello,

is there anyone that can reassure me that they had treatment  without a feeding tube? I couldn’t tolerate the ng from constant retching so had it removed but problem is it doesn’t look like there is availability to get a PEG instead! I might be wishful thinking…..

  • I can't think of any names off the top of my head I'm afraid Clare, but without question some do manage to get through without a tube at any time; so it's certainly possible.

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    Metastatic SCC diagnosed 8th October 2013. Modified radical neck dissection November, thirty-five radiotherapy fractions with 2xCisplatin chemo Jan/Feb 2014. Recurrence on larynx diagnosed July 2020 so salvage laryngectomy in September 2020.

    http://mike-o.blogspot.co.uk/

  • Thanks Mike. Perhaps if I really struggle they will manage to fit me in! 

  • Without a doubt, they'll take whatever steps are needed to keep weight on/minimise loss.

    I was admitted for the last four days of my RT due to weight loss; my wife phoned my dietician and I was on my way in half an hour. I already had a PEG but couldn't get enough down, so they switched me to overnight pump feeding; made life a lot easier once an optimum flow rate was settled on.

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    Metastatic SCC diagnosed 8th October 2013. Modified radical neck dissection November, thirty-five radiotherapy fractions with 2xCisplatin chemo Jan/Feb 2014. Recurrence on larynx diagnosed July 2020 so salvage laryngectomy in September 2020.

    http://mike-o.blogspot.co.uk/

  • is there anyone that can reassure me that they had treatment  without a feeding tube?
    1. Yes Clare. There are a few.  I can remember  offhand and there are a few chaps but like Mike my heads a sieve these days. I managed three weeks nearly four before it all came crashing down and I had an NG tube. I didn’t notice it at all in my throat amidst the pain of mucositis. 
      There are hospitals that refuse feeding tubes unless you are in real trouble so it is possible. I was warned that if I lost more than 5% of my body weight I would be hospitalised. It was a no brainier to stay at home. 
      Line Mike I was pump fed  at night. It was a godsend to not have to worry about dosing myself with food during the day 

    Dani 

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

    I BLOGGED MY TREATMENT 

    Macmillan Support Line -  0808 808 00 00 7 days a week between 8am-8pm

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  • Thanks. Perhaps they’ll do the stomach PEG if I’m desperate which I’m more than happy to have. Just not the throat. Even the doctor said I couldn’t continue like that. 

  • Hi Clare

    I only had an NG tube for a few days while in hospital after surgery.  I started radiotherapy 6 weeks later but didn't have any sort of feeding tube for that.  It was tough going and I lost a lot of weight which I didn't have to lose in the first place!  There were mutterings towards the end of treatment about having an NG tube but my weight just about managed to stabilise.

    I can't remember whether you've started radiotherapy yet?  The website used to have the facility to see old posts from people but I can't find that since the recent revamp.  Sorry.

    Linda x

  • Thanks Linda, that’s really helpful.  yes tomorrow will be three weeks. Are you fully recovered now? X

  • I might be worth asking whether there's any possibility to have a PEG fitted should things get too difficult Clare.  Hopefully you won't need it.  

    I finished my treatment in August 2018 and all my check ups have been clear, thankyou.  A few residual problems that I'm working through.

    Sounds like you're doing well so far.

    Linda x

  • I can't remember whether you've started radiotherapy yet?  The website used to have the facility to see old posts from people but I can't find

    Hi Linda. I keep forgetting you managed without a tube. Brilliant. 
    Re past history it still works. 
    Click the persons avatar click on more then activity and keep scrolling to bottom of the page. 

    Dani 

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

    I BLOGGED MY TREATMENT 

    Macmillan Support Line -  0808 808 00 00 7 days a week between 8am-8pm

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  • Hi Mark777 refused anything like tubes he was close but did manage from memory. O hadc2 guys with me both lost a lot of weight and struggled in recovery but got through it. It all depends on your oncologist how much weight you are loosing. My n g tube was out in end of week 3 I never felt it maybe if yours was after surgery ? It may be worth trying it again if they can’t do a peg ?

    Hazel x

    Hazel aka RadioactiveRaz 

    My blog is www.radioactiveraz.wordpress.com  HPV 16+ tonsil cancer Now  6 years  post treatment. 35 radiotherapy 2 chemo T2N2NM.Happily getting on with living always happy to help

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