My husband just completed day 15 of radiation treatment for hpv tonsil cancer. He is really starting to have side effects and is trying to figure out what he can eat and what he can't . Cheerios and milk and a smoothy so far go down pretty well. We just saw the dr who adjusted his pain meds and he just tried the magic mouthwash for the first time. This is all so overwhelming, but I know we will get through it. We are staying with our daughter as she lives much closer to the cancer center. Our other daughter and son live closeby and we have two grandchildren who give us joy when we are feeling low. Thanks for listening!!
Hi welcome to our small friendly community group that none of us wanted to join. We’re always happy to help no questions too silly ask. I’m 7 years post chemo radiotherapy tonsil cancer. Am living a great life now. Hugs
Hazel xx
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
Thanks for listening
Hi again Rara2
Thanks for your update.
That’s another week done so your husband must be half way through.
A day at a time. Hugs
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Hi Rara2, seems like things are going pretty well.. your husband is entering the nitty gritty stages now though, so don't be afraid to use the PEG for overnight feeds if things get tough, and just continue drinking if possible... take the meds by the clock and keep on top of the laxatives, he will not want constipation on top of everything else..
Loz (62)
Oropharyngeal right tongue base T2N2bM0 squamous cell carcinoma p16 positive..
Thanks for this update Rara2 and well done to your husband in getting this far, he will start to feel the side effects kick in a bit more so its good to hear his pain meds have been increased. He could ask for food supplements if the swallowing becomes difficult as they will help him to maintain weight. It must be a big help having your family with or near to you as it will help take your mind of the treatment. Wishing you all the best for the remaing treatment and recovery, take care.
Chris x
Thank you for your encouraging words. It really helps!!
No PEG. I am from the US, PEGS are not offered immediately. I know all of you here say they are life savers. I will keep you all informed. Thanks for the support!
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