Do you have any questions about radiotherapy treatment? Ask our volunteer radiographer...
Ask about treatment, speech, voice, or swallowing difficulties during or after head...
Ask our volunteer Dietitian, Alice, your questions about diet and cancer and she...
Do you need advice on how to look after your mouth during cancer treatment? Or for...
Hi madaboutmutts. Fingers and toes x youve come this far ,I am now 15 month post radiotherapy and living my life ,ok reduced saliva and still some food issues .
look forwards to hearing your news next week.
try nit to stress
Hazel aka RadioactiveRaz
My blog is www.radioactiveraz,wordpress.com.
i give a honest account of my experiences with tonsil cancer
HinBluebird fingers x for pet ct scan , I was lucky in a way my oncologist made me wait 17 weeks as he said if he did it before xmas Iin early dec it was too early at 12 weeks as too many false positives come in his experiences for mr I . So,I had my pet ct scan 4 jan results 14 jan and hasn’t he promised me in day ine no signs of cancer remained . All my follow up appointments have been good , so try and take positives and fingers and toes x . Ye agree sometimes to consultant s become immune to patients feelings try and enjoy Christmas , just remember how far you have come since the start if this treatment .
Keep in tiuch
Bluebird6 when I had my PET scan I had the contrast, as well as with my CT and MRI scans
Thank you Hazel. So hope I will have good news to post next week!
Hi Hellibore1 and interested others
Hubby is now 10 weeks after chemoradio treatment 30 radiotherapy & 6 chemo over six week period - this followed surgery for removal of both tonsils. His was SCC & HPV positive. Final diagnosis was Advanced but locally contained cancer - with 3 lymph nodes confirmed and two suspected.
Following treatment and the usual follow ups we have asked if any scans were planned. Usually reply was we will see, leave it for now.
The last follow up was with the original diagnosing Head & Neck surgeon who totally shocked us by his responses to our questions. He initially ruled out any scans saying not necessary, then when my husband explained why he thought a scan was necessary he could barely contain his annoyance and asked what type of scan did we want. When we said PET scan as that showed up where the primary tumour was (previously CT & MRI hinted but couldnt diagnose) he was adamant that we weren't going to get another PET Scan and ordered an MRI.
We are aware that PET scans are expensive and as the margins of the tonsil were positive for cancer cells it seemed reasonable to ask for that. It seems to be a postcode lottery relating to scans from what we can gather.
The information you provided in your post is highly relevant to my husband (and obviously others) and we may delay the timing of the scan - especially if a contrast dye is to be used.
Thank you for your positive words, we are keeping a positive focus and very hopeful for good news in the new year , just crossing everything and trying to keep busy!
Hi Brandy Girl
your husbands experience sounds very similar to my husband in relation to the treatment. I asked a while ago for a pet scan for my husband but they seem very reluctant even though many centres seem to be doing PET scans as a normal part of the process. As you say it seems very much a post code lottery which is disappointing given the NIce guidance that is available. hope you get the scan and the results show good news for you both. Hope we both get good news in the New year!
Thanks Rob , always helps to hear others experience
thank you! Will keep positive thoughts ! I’m very hopeful!
Hi Brandy girl
so sorry your consultant was off hand it isn’t fair ok they may see people daily but at that moment in his day you are his patient.
My oncologist was brilliant at Leeds cancer centre on first day he explained everything that would happen even that we would be waiting 16/7 weeks for final pet ct scan as he didn’t want false positives showing if it was done too early. So if mri with contrast is what yiu will get do try and get it done later rather than sooner if waiting a few weeks longer gives you peace if mins it’s worth it.
Pleaes hubby now at 10 weeks m remember the h o v diagnosis does give us head and neck patients that extra positivity,
if any consolation my local ent appointment last week ( now back at local level ) consultant wanted to see me 11 Feb next year ok I though . So imagine my surprise this afternoon when postman delivers nhs letter Cancelling my 11 Feb appointment with comment we can’t offer you any further appointments At this time. .Ummm git anither 4 years of this !!
Best wishes and keep positive
My husband got his PET scan results today. Not entirely good. His lymph node has gone but tiny hot spot where his primary was (L tonsil - which was removed) He still has a very sore throat. ENT surgeon did a scope and said nothing looks suspicious but to be sure they will have to do a biopsy after Xmas as it was a bright hot spot. The Consultant said he has a lot of ulcers in the throat on the scope. I asked if it could be a 12 week false positive and he said hes quietly confident it is. But if that's the case why did they not just suggest a further scan in a few weeks! He said they have to be sure but if it was cancer it would still be curable. We had pinned so much on a clear result and I so wish it had been done a few weeks later. My mind is in overdrive and I dont know how we will get through the next few weeks. Has anybody else had this?
Hi don’t stress , I haven’t but my oncologist did say it’s quite common if pet ct scan done too early. With mybscan date being 4 January we did ask if it could be done earlier prior to Christmas and to be honest he was right it out for that very reason I was 17 weeks. By the time mine was done. Going from memory the figures he quoted to me was 60% come back if done early . So take comfort from his words quietly confident. Just remember how far yiuve come since the early dark days.
Sending hugs Hazel xx
False positives are really common at 12 weeks. Some hospitals are now routinely doing PET/CTs at 16. I had mine at 16 and it still showed a hot spot. There is a protocol in place for this and taking biopsies is part of this protocol. Wait and watch is too risky. Having said that I was in exactly the same position as your husband. I reacted badly to the radiation and my throat being badly ulcerated took a long time to recover which is why it still took up the radioactive glucose. On the scope my throat looked good. My biopsies were all negative. I’m sure your hubby’s will be too so try not to worry.
Hi. Sorry this is proving to be so stressful. I had the same - a hot spot in tonsil area on 14 week PET (after an indeterminate MRI for neck at 12 weeks), but I was strongly reassured that this was likely to be scarring from the chemoradio. They didn’t offer a biopsy and said they would just evaluate the hot spot area at each appointment - I then pretty much insisted on a repeat PET 3 months later which was entirely clear. I think the docs are in a difficult place - if they scan everyone later than 12-14 weeks, the occasional patient who has not responded to treatment and still has cancer will be left with disease for longer, risking their overall survival. But by doing an earlier PET they know they will have many false positives in area of original tumour which causes a lot of anxiety to us the patients. What’s the right answer? So please be reasssured that hot spots in tonsil region are common and will almost always resolve - you have the additional reassurance that there is nothing to see that is suspicious.
Easy for me to say, but relax and look on the bright side -its highly likely to go away as the scarring heals, you will not do any good by dwelling on the small chance that there is more disease, and you cannot change the outcome. They do know what they are doing ( mostly). The neck lymph node is the real issue at this stage - and that has gone Hooray! Dwell on that and enjoy Christmas as much as you can. Get zopiclone for sleep if needed and maybe try to access some counselling or talking therapies - I was never one for such stuff.....until scanxiety set in and a counsellor was very very helpful. That 3-4 month post-treatment time was a horror for me so you have my sympathy. But now I’m more than 2 years post-treatment and leading a pretty normal life, punctuated by the odd treatment effect!
Best wishes to you both,
Thank you all so much for your reassurance. The consultation was pretty rushed (end of day at 5 45pm) and we were not shown the scans or able to ask many questions. Husband has done so well throughout the treatment and we were quite confident of a good result. We didn't see an Oncologist - just the ENT surgeon, and one we had not seen before. OHs throat still very sore and ulcerated so maybe this is why there was a take up there? In any case nothing we can do now but wait, hopefully 2020 will bring good news x
Safe payments by:
We're here to provide physical, financial and emotional support. So whatever cancer throws your way, we're right there with you.
© Macmillan Cancer Support
© 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: 89 Albert Embankment, London SE1 7UQ. VAT no: