Hi
looking for any tips on food and drink.
I’m 5 weeks into radiotherapy and have NG tube, feeding overnight. I really want to eat and drink but struggling with pretty much all food. Hot chocolate is the only thing that goes down well. Fizzy drinks I can’t manage, nothing citrus, everything tastes foul. I’m wasting so much stuff as I think, ooh I’ll try that but once it’s in my mouth that’s it-done! Thanks
Hi ER1,
I'm approaching week 3, taste is out the window yet i can still eat. I'm finding anything really bland works, mashed potato with full fat cream, tinned rice pudding was a nice surprise and ready brek still has its taste. I'm chewing all sorts of sweets just for the exercise but they become awful. I've resigned to the rig as had a tearful day and was losing weight fast. I've been trying to hang onto eating but as Hazel says, we need the calories! X
Hi Shab...yes the taste thing is just about par for the course,careful with those sweets if they have sugar in them. Have you been given jaw and swallowing exercises? I did those when I stopped eating. I relied on being pump fed at night and played with what I could eat and swallow knowing I didn't have to "eat" enough to survive
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Hi beesuit, you're right re the sweets, sorry I didn't mention they're sugar free. It's purely so I feel like I've actually chewed, as well as the exercises of course. Especially for the swallow. It does take some of the nasty taste away too which helps. We've had nutritia nurses call to go through things but they didn't show us the pump as we weren't there! We've mentioned it at the hospital but i'm managing with the bolus feeds for now. Its all very trial and error as to how much you can take at one time! x
Hi Sharon.You’re on track lack of taste isn’t unusual to have gone by this stage I was and still are one of the odd balls I never lost taste but have accentuated taste.
by end of week 3i was getting most of my nutrition and hydration from ng tube. You’ve got it use it. Sweets sadly will harm your teeth as lack of saliva causes decay. It’s a life long balance. You should have been given exercises for swallow and jaw I used to do mine on way to treatment and fitted them into my oral routine still do them even now not as often my mouth has never had an issue opening ! You can tell I type a lot plus I talk a lot .
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
Yes just do what suits you. I never fed as much as I was told to. Couldn’t take the volume. I asked to be pump fed over night as I was fed up trying to fit small bolus feeds in between all the other stuff
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Hi Hazel, I really thought it was the chemo that's given me the most problems.
The sweet thing is my way of doing extra exercise, it's the strangest thing not chewing to eat. I'm only drinking zero sugar coke and water. My smell sense is on overdrive! X
My smell sense is on overdrive! X
It was the only way I could taste in the early days.
I used to blow air the wrong way back up my nose. While I chewed
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2026 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007