Hi, my husband is currently on week 5 of radiotherapy for treatment for tongue cancer. He is doing well despite big weight loss and only receiving food supplements through his feeding tube into his tummy as not able to eat/drink orally. Biggest problem he has is fast amount of saliva in his mouth which is really unpleasant for him. Just wonder if anyone else has experience of this and has any useful tips to help?
Hi Shazz sadly it’s a common side effect I spent weeks spitting into tissues or grossly putting fingers in mouth to pull the stuff out. I had a humidifier for bedroom and a nebuliser which hospital have me I used up to 6 a day. Plus carbusistine to thin the mucus down. You can steam over a bowl of water with towel over head as well. Don’t put any oils ir anything in either hot water ir humidifier v it dies go as quickly as it came often replaced by the dreaded fry mouth. Mine lasted up until around week 8 of recovery some go quicker some longer. Well done on getting to week 5. Remember after treatment finishes recovery isn’t straight away it does take time.
any questions just ask.
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
There's no real way too stop it. If it's thick and causing choking then thinning it with water whether it's steam or just drinking as Hazel says can make it more manageable. It's just a case of spitting it out. I carried wads of kitchen roll around with me and slept with a roll by my bedside. It went as quickly as it came. Salivary glands make two sorts of saliva. Water with enzymes and mucous. The watery bit gets knocked out first by the RT and you get left with thick mucous for a while. That's why it happens. It will get better
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Thankyou for your help. He has tried the steaming but didn't seem to help much. He is also struggling to drink any water as swallowing very difficult hence everything is going through the feeding tube in his tummy. Guess just spitting it out is all he can do for now plus using the mouthwash 3 or 4 times a day?
Thanks Hazel, sounds like no easy answer to this is there? Awful for him & for me watching him suffering. Guess we just need to ride it out & hope things improve in time.
HubShazz sadly there isn’t it’s a case of riding out the storm. I was putting at least 3 litres of water in my my feeding tube every day.
Maybe try nebuliser ?
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
Horrid but spitting is what we do. There’s no other way. There’s no magic remedy. Just time.
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
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