Hi , had my last chemotherapy last Thursday did 5 out the of 6 planned as Doctor said another would be too much for me , on my 6th final week of radiotherapy , after effects aren’t so nice as many of you know . Last night I had really bad Saliva/ mucuses which made me retch not sure if this is chemo or radiotherapy causing it , have had it throughout but not this bad , bit uncomfortable as got nose/stomach feed tube. In. Have tried nebuliser, is ok but just trying anything to ease it , had to have another mask fitted for my last week and half , as lost bit of weight around neck/face . Any advice appreciated thanks Ozzer
Hi Ozzie sadly there not much you can do. Try drinking water or I found flat Diet Coke helped disperse some of the mucus or soda water if your mouth can take it. As for nebuliser I used it uo to 6 times a day plus was prescribed carbusistine to thin it .jury’s out if it worked but worth trying. I also used my fingers to pull the mucus out literally nit pleasant but needs must. It does give as quickly as it came often replaced with dry mouth. It’s the radiotherapy that’s the main culprit not chemo. Remember once treatment finishes you usually feel pretty crap for a good few weeks so don’t plan doing too much I slept a lot if the time inbetween hydration and oral health care.
Good luck with last week.
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
Hi Ozzer,
I'm 4.5 weeks post treatment and had the most terrible mucous from about week 5 of RT (I had 7 weeks). Time scales will vary for the mucous to clear but I woke up Saturday morning (4 weeks post treatment) and had the driest mouth I can ever recall! It has all but cleared up as suddenly as it appeared! It will go, just needs time :)
Hi
my mum had very thick saliva/mucus during radiotherapy (tongue cancer, subtotal glossectomy and total neck dissection) which became really bad from about week 5 of radiotherapy onwards. We found using a humidifier overnight, frequent nebulisation plus using pink foam ‘lollipops’ to scoop out the saliva/mucus helped more than anything. She also has a g tube and is nil by mouth so couldn’t sip anything to help.
For her the affects significantly reduced about 2 weeks after radiotherapy finished. She is now 5 months post radiotherapy and although still has problems with this, it is 100% better than it was. Fingers crossed you can find somethings that work for you and like mum you see things ease once therapy is finished!
take care
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2025 © 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