Hi everyone
I’m 9 weeks post surgery for ACC and my hearing went in one ear 4 weeks ago and this last week my swallowing seems to be getting worse. I thought I should be ok by now?? Tried popping my ear and had popped a couple of times (hurts when it does) but lately unable to pop them. It’s driving me nuts and my family as I can’t hear them ?
The whole area inside/outside remains numb since surgery.
any advice would be appreciated
thank you
It's good to be aware of the side effects Elaine but do remember not everyone has all the side effects to the same degree. If you can, take each day as it comes and seek help and advice when you need it.
As I'm sure you realise, you'll find lots of help and support on this forum from people who have had similar experiences as well as from your team.
Take care.
Linda x
What are you doing to improve your swalllowing -- besides loads of pain relief, that is? I've recently come out of extensive surgery for oropharyngeal and neck cancer and was left with one huge problem: swallowing sufficiently strongly to get liquid and foods down. I've devised out of pure necessity a couple of management techniques and would be happy to share them with you.
There is a range of swallowing exercises that our SLT should give us. I did mine religiously through treatment and still fo them now three years later. It’s just part of the daily routine
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
To be honest was on pain relief for 9 weeks or so and I’m not convinced it does much for the type of discomfort I get which is a stretching and aching feeling. brufen and paracetamol don’t help. I avoid stronger stuff as I think my discomfort now is something I should get used to and live with. Don’t want to be hooked on drugs that make me constipated. I do have amitriptyline however whether that helps who knows but it helps me sleep. Of course once the radiotherapy side effect come I’ll pop the pills again and take them regular if or when it gets painful.
when swallowing fluids I need to concentrate so it doesn’t come down my nose , foods ok but need plenty of water and obviously some foods are better than others.
Hi Linda
I saw them pre op and a week after discharge. I got a leaflet with some exercises to do. I’ve been doing them and can now open my mouth 2 finger widths and get a fork in so much better. I think I’m getting a phone call tomorrow by salt pre radiotherapy starting. It’s a different salt as had op in regional hospital and radio in local hospital.
thanks
Elaine
Do tell them about your swallowing. It would be great if you could get an appt to see them so they can experience first hand your swallowing and give you some proper one to one advice and ways to make things easier. They would also be able to give you proper instruction on swallowing exercises.
Linda x
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