After finding out in December 24 that my amazing husband Martyn had tonsil cancer. It’s been an awful rollercoaster to be on. He completes today 6 weeks of daily radiotherapy and weekly chemo for 5 weeks. The side effects are not pleasant,mainly the horrible mucus and the terrible sore throat and swallowing issues. His skin so far hasn’t broken but is red and leathery, constant moisturising has kept it intact. The feeding tube has been challenging but the overnight feeding has made it more manageable. I think he has been incredibly brave and strong, at 68 years old. Now he needs time to start his recovery.
This site has been an amazing source of information and reading other people’s stories has at times been very humbling. So where ever you are on your cancer journey please believe you are not alone. There is always someone on here to help you out. God bless you all ️
Hi Miserable.
I can tell how proud you are of your brave husband, and rightly so. He's reached a major milestone and I wish you both the best of luck with his recovery xx
Two weeks ago, when my lovely man finished treatment, he rang the bell and then we hugged and cried our eyes out! I still tear up every time I look at the video I took. To celebrate his achievement, we went to the cafe, in Bexley Wing at Jimmy's, for fish and chips. He struggled to eat his as his appetite had started to wane, but like in everything else he's done on this gruelling journey, he made a supreme effort.
So, enjoy and celebrate with your Superman for reaching and clearing this hurdle.
Hugs to you both and all the luck in the world!
Gill xxx
That’s huge news. Now just hunker down and heal. I was 68 when I finished my six weeks RT
I largely slept for the two weeks after and the same way you are looking after your husband mine looked after me. Hooked my pump up at night and fed me morphine through the day. Carers get a rough deal but all us patients know how brave they are. Hugs for you both.
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Well done to have come so far. My husband is now 15wks post treatment. The side effects will still be with him for some time,dry mouth,no saliva,coughing because if the dry mouth,on the plus side the tiredness and fatigue is gone,finding a normal sleeping pattern now. He still uses his PEG, but we are finding more and more food that he can have and taste. We had some good news from our latest appointment with our consultant,so the treatment was cruel, but it did it's job. So persevere and take one day at the time,you will get there. Hooe you can enjoy the easter break. Hugs, fellow wife Mel xx
Gill H. Aah thankyou that is so kind of you. My husband would love to be able to eat fish and chips,hopefully that will come in the near future. Wishing your husband a continuing good recovery. Best of luck for the future to you both ️
Much love
Sue xx
Hey, Sue.
Did your husband bring his RT mask home? Mine did. Some might find it a grim reminder of a traumatic time but we decided to try a different approach and even named his mask - Noodles! That's because the mesh looked like Super Noodles.
It takes all sorts, but we try to inject a little humour into a ghastly time to keep ourselves sane. I even refer to his copious mucus secretions, which I mop up endlessly, as 'snakes and worms', but I won't go into that...
XXX
congratulations.. there's no doubt that it's a tough gig.. there's still a couple of weeks to go that will be a bit of a challenge, but don't despair, you're on the right side of the journey now, and on the road to recovery.. just be patient and don't try to rush things.. healing will take time..
Loz (62)
Oropharyngeal right tongue base T2N2bM0 squamous cell carcinoma p16 positive..
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