My husband will be starting radiation later this week. I am trying to be supportive, but am scared of all the side effects he may experience. How does everyone take it "one day at a time?" He has tonsil cancer and it is stage 1, not operable.
Hi Rara welcome to the club none of is wanted to join. It’s rare that tonsil cancer is operated on so don’t worry about that. Radiotherapy is the gold standard treatment. I am almost 7 years post treatment.
One day at a time is the only way you can’t control what’s happening it really is one day at a time.Trust his team they are the experts they do in daily. Take heart from us on here head and neck cancers do respond very well to treatment we’re proof of that fact .All you can do is be there for him but at same time look after yourself I encouraged my husband to give us both some space he use to meet a friend for coffee to get out of the house. Treatments is hard but I went through it and he will too. Stick with us always happy to help.
hugs 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
Hi Rara. We do get through a day at a time. I had six weeks of RT and just ticked the days off
Nothing much happens for two weeks then your throat gets more and more sore.
Is your husband being offered a feeding tube g tube? If he is tell him to grab the chance.
The treatment us a real challenge but it doesn’t last forever.
You will surprise yourselves with how well you both get through.
Thus is a useful thread
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
My trust didnt routinely fit feeding tubes but I had to agree to a ng tube is needed and it was needed. It was my lifesaver and allowed me to continue treatment from week 3 and uo to week 3 recovery. It took the worry out of trying to eat and swallow it also helped my recovery immensely so please do t let him tough it out as it’s nit easy trying maintain weight take sufficient calories. Read my blog below for more info
Hazsl 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
He has not been offered a feeding tube and wants to continue to try to swallow throughout the treatments.
Some people do manage but not many. I hope he has it in his mind to go with a nasogastric tube if needed.
I know some people need the fight to maintain some sense of control and get through.
Keep us in the loop. There’s always somebody here to talk to
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
I can only endorse what the others have said re feeding tube. My Trust fitted them routinely. I didn’t want one…in fact to say that the idea horrified me was an understatement. My oncologist was insistent and for that I shall be forever grateful. I would not have survived without it. I hope your husband does manage his aim of getting through without…but please don’t let him be stubborn if it becomes too much. The tube for me took the apprehension out of food and, I think, prevented my developing a real problem with it.
As others have said, one day at a time really is the only way. There is a certain satisfaction in ticking off the days, particularly once you get past the half way mark.
Please look after yourself too. In so many ways it’s harder for partners than for those actually going through the treatment. I know it was for my husband.
All the best to both of you. It’s not a walk in the park, but we come out the other side and, as has been said, success rates are high.
Liz
Hi there, I feel for for you and I am so sorry about your husband having to go through this,my husband finished his treatment (30rounds RT 2rounds CT) 7wks ago, yes it's true each patient heals different, but I am not gonna lie,it's just as hard to see your loved one having to deal with the side effects, I am having to take day by day, we have better ones and then the not so good ones, our consultant told us straight from the start that it could be a long bumpy road to recovery, he knew what he was talking about, some days I find myself crying to sleep. I have to stay positive and strong for the both of us. Reading some of people's stories on this forum gives me some hope. So stay strong and positive and do take on day at the time. All the best Mel.x
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