Hi, I am one week into radiotherapy for SCC of left tonsil bed and left neck lymph nodes. Tonight I’ve noticed a very small node on the right hand side of my neck, it feels exactly like my initial symptom was on the other side. I’ve messaged the hospital about it, but obviously I’m really worried about this and just wondered if anybody else had had a similar experience, and if so what was the outcome?
Bridget
Hi Bridget
I think we all become very sensative to any changes in our H&N areas when we have cancer. Every lump and bump worries is.
You have done the right thing by contacting your team, but I suspect that the treatment has irritated your neck and that it's what you're feeling. Fingers crossed that is what it is and you'll have an answer tomorrow when you attend RT.
Hi Bridget. I was scanned weekly usually a Monday whilst on the radiotherapy table the the table was finally tuned . Mention again to the team in case message hasn’t been passed across. I saw my oncologist or his registrar weekly as well during treatment so re iterate to them. To be honest I don’t think I touched my neck during treatment as everythjng felt strange .
best wishes s for week 2
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
Thanks Peter, I really hope your suspicion is right but the worry is that it’s on the untreated side. I’ll update this post tomorrow.
I had 75% radiotherapy on cancer side and 25% on other side ask if you are having same? But do point the new lump out to them
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
Thanks for the message Hazel. I was scanned last Monday, before my first treatment, but I was told that the scans in the radiation room don’t show the tumours, only bone, for the purpose of alignment. At my hospital, patients don’t see oncology until the beginning of the third week, but I have emailed the fabulous Macmillan Nurses there and I’m sure they will be on the case tomorrow. I will also mention it when I go for radiotherapy.
Best to be on the ball. Try not to worry they will be in the case tomorrow I’m sure.
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’m only having it on the left side (same side as my primary on the tonsil, and the neck metastases). Thanks to you and Peter for your kindness in replying tonight. I’m going to see if I can manage to sleep now, thankfully my appointment is early tomorrow morning so hopefully something will start to be done to either put my mind at rest, or alter treatment plan.
By the time I arrived for radiotherapy this morning, the radiographer had received an email from my consultant saying that the CT scan I had six weeks ago when my mask was made, didn’t show any abnormalities on that side of the neck. They’re going to leave it for a week to see if it gets either bigger or smaller, and I see the oncologists next Monday and may then possibly be booked for a biopsy and/or ultrasound. The thing that worries me most is that, on my PET scan result from October, it said that there was a “mildly avid”node on the right. Mildly avid usually means that it’s just a node that’s reacting to slight infection or something going on in the body. But as it showed up on the PET scan, I am worried that it could well have been the cancer just starting up on that side. The radiographer said that the oncologists wouldn’t want to disrupt my current treatment, and it’s likely that I would have to finish it and then have more on the other side if it was cancer, or possibly have it on both sides for the remainder of treatment, but it would depend on what they find out. I have managed to stop worrying about it now that I know it wasn’t seen on the CT scan six weeks ago, but then I get a bit anxious because a CT scan doesn’t show up everything that a PET scan does. So the saga continues……
Thanks to those who have commented on this thread, it’s so good to have the support of this forum, it’s invaluable x 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