Hi,
I am 29, Female. I had a lump cut out of my cheek on the 15th of March, I was in yesterday for my results which was given as a salivary gland cancer. Which hit my like a bus and I did not expect. I had no other symptoms other than a hard lump which was painless.
I am waiting for a MRI, chest X-ray and then discuss a treatment plan monday PM.
Could anyone with the same/similar diagnosis advise on what treatment they went through. I am so scared of what to expect.
thanks S x
They haven’t ruled it out but I’m keeping my fingers crossed :) thanks for replying.
theres a couple of things I don’t understand and not sure if you could help me? Before I speak to my macmillian nurse when I see her. I know I have to attended for 5 years but when do you hear an all clear result, I was under the impression it could be after surgery / radio but I hear I could be wrong. Sorry for sounding niaeve but I haven’t really been around C. My grandparent had it but it was too late for treatment x
That will be a great result if you can avoid radiotherapy. Hoping the surgery goes well.
This is great news that it has not spread, good luck with the upcoming surgery and hoping they manage to remove any stray cells so no further treatment is required, wishing you all the best,take care.
Chrisx
Hi When I had my pet Ct scan 17 weeks after treatment finished I got the NED which is no evidence of disease which is as good as one can get, The words all clear aren’t used , after 5 years of being monitored I will be discharged from the cancer team. But will always be able to contact them if I have any immediate concerns. That’s the point I will be in my mind all,clear. Hooe that’s helps. Fingers x for no radiotherapy.
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
Thanks Hazel, yeah that makes sense. I was shocked when they said I have to attend for 5 years but I suppose it’s really good to be checked on. And thank you
hope your well x
It is often a pain the the butt having to plan around the checks, especially in the first year or so when they are every 2-3 months, but they are so essential to your wellbeing. My return of cancer was picked up at a routine check before I even realised I had something wrong. Don't skip the checks and don't be afraid to contact your team between routine appointments if you have any concerns.
I was shocked when they said I have to attend for 5 years but I suppose it’s really good to be checked on. And thank you
hope your well x
And after.
Most teams will let you keep in touch after discharge.
My oncologist has told me that although I won’t be on his clinic list I remain his patient and if there is anything worrying me I should bypass my GP and contact his secretary
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Oh that’s brilliant. I had a call from my surgeon secretary today, to advise me to be in for 7:15am on the day of surgery with the hopes I’ll be out the same day which would be me feel so much better. I remember the specialist saying ill be absolute sick of him by the time I’m done haha x
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