Hi Everyone,
It's so good to hear everyone's different and similar experiences and advice. It makes the whole RT thing seem a lot more surmountable, when I see all you who have got through it X
I was wondering whether anyone here experienced any sort of hearing loss, either as a result of surgery or RT?
I seem to be getting deafer and deafer in my right ear ( the business side), which started before RT but several weeks after surgery, I think it actually coincided with when I started with the Therabite, so it may be causal or just coincidental. Who knows?
Anyway was just wondering what people's experiences and outcomes were?
Thank you
Rx
I think they do downplay this side effect. When discussing chemo and my fear around hearing being hit my oncologist stated that in all his time treating people only one had had any effect. Hmmm. The number of patients I spoke to during my treatment that had their hearing affected by Cisplatin was quite high. Glad I went for Carboplatin!
I think they do downplay this side effect. When discussing chemo and my fear around hearing being hit my oncologist stated that in all his time treating people only one had had any effect.
Quite different from my oncologist. He was quite upfront about it and any patients with existing tinnitus were like you offered carboplatin. I avoided chemo but I spoke to others who were told to speak up if their first cisplatin caused problems.
I remember going through my consent form to be told that cisplatin was ototoxic and that effects could be permanent but that it didn’t matter to me.
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Hi I had 2 of a planned 3 cisplatin chemo when I was signing consent for I was told I may get tinnitus and at first inkling of any issues with hearing to tell oncologist. When we were discussing my 3 rd chemo we jointly decided not to have it my big lump was no longer palpable and I had got through the first 2 chemo relatively easily and no hearing issues so we chose to cancel the 3 rd chemo. I’m ok after radiotherapy as wrll
ny hearings as good as it was prior I’m lucky I do realise.
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
I had hearing loss before I had surgery and then started radiotherapy on the right side of my neck and jaw. Afterwards, I had lost a lot more hearing in my right ear, and it has deteriorated in the almost four years since. The audiologist says I have become profoundly deaf on that side. Sounds also get distorted in that ear. Hearing aids help with conversation, but some genres of classical music are unpleasantly affected. As far as I am concerned, this is a small price to pay for what I hope has been successful treatment.
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