Radiotherapy and chemo has anyone not had a peg tube?

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My hubby has squamous cell carcinoma in his left tonsil with secondary in his neck (a lump) he’s opted not to have surgery but to have radiotherapy and chemo instead. 6 weeks of radiotherapy, 30 sessions and 6 weeks of chemo, once a week. 
he is determined not to have a feeding tube of any kind fitted. My question is how may have managed to undergo similar treatment without a feeding tube? How was it ? What meals did you eat? Sorry for so many questions but I want to be prepared. Many thanks. 

  • Hi it takes a while for the planning to get done and a slot to  become available on the Linux machines. In scheme if things it won’t make a difference.  I was 63 days from diagnosis to treatment starting. The next few weeks  at least hubby can eat what he wants !! 
    Hazel 

    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

    2 videos I’ve been involved with raising awareness of HNC and HPV cancers 

    https://www.instagram.com/merckhealthcare/reel/DBs8Y0niJ8N/

  • My timing was similar, I had dissection at the end of November 2013 and started radio/chemo on 13th Jan, they told me to over-indulge as much as poss over Christmas....so I did.

    Just as an aside Cat, we've had a couple of Royal Surrey patients on here before so I've mentioned that I was brought up in Guildford, are you local to there or making a bit of a journey in?

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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/

  • Hello Janene, i hope you dont mind me asking but did they explain the removal of the tumour compared to the treatment using radio and chemo. I understand if you don't want to reply. I have always given a PEG but there are quite a few who did not and got through it ok, what he has to realise is that both his neck and tonsils will be treated at the same time. There is always the option of the NG tube if he does struggle with swallowing, this does not require any surgery and can be fitted quickly and easily. Wishing your husband all the best, take care.

                                                                     Chris x        

    Its sometimes not easy but its worth it ! 

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  • Hazel may be right with the PEG but NG tubes can be done in out patients. My trust protocol was to be reactive and place feeding tubes if they were required but they never refused them if they were needed. I ended up in hospital for a few days because I got dehydrated over a weekend when I stopped taking anything orally for two days.I was admitted on New Years eve and had to wait till the 4th to be discharged because all the nutrition staff were partying

    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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  • FormerMember
    FormerMember

    Hi, I had similar but opted for surgery and adjuvant IMRT. Then chemo came later but that’s another story….::

    I had very few mouth/throat issues and was able to eat normally throughout the 6 weeks of IMRT. It’s very targeted these days. So horses for courses but don’t assume a PEG is needed 

  • Hey Richard. Just like to say Hi and keep going. And give you a hug. Xx

    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 Richard good to hear from you 

    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

    2 videos I’ve been involved with raising awareness of HNC and HPV cancers 

    https://www.instagram.com/merckhealthcare/reel/DBs8Y0niJ8N/

  • Hi Janene

    I had the same diagnosis and symptoms 

    I had the surgery and all of the tumour was removed and I have not needed radiotherapy or chemotherapy.

    I cannot answer your questions about PEG feeding as I did not need it, it took a few weeks but then managed to eat normally 

    You will get excellent advice on here

    wishing you all the best 

  • Hi janene123

    i didn’t have a tube.  They don’t fit them as routine at the Marsden, although I did ask about it.  I did manage to eat weetabix with cream snd protein powder all they way through and didn’t loose any weight.  Also jelly snd cream.  Hope this helps.  

    lizzie223