Im not in UK, but your space was highly recommended and I hope it’s ok I am here…
63f, HPV+ SCC left palentine tonsil, local lymph node involvement. Heading to 2nd consult next week. Weighing all my options.
everyone is welcome here good luck with your consult
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I'm 21 yrs post transplant - High-dose BEAM + autologous stem-cell transplant 2004 (age 23)
Diffuse Large B-Cell stage 3 high grade Non Hodgkin's lymphoma
Hi PassengerPigeon, of course it's ok that you are here, and you are very welcome. You can ask or say anything on here, we are all here to answer any questions or offer any advice we can. When or if you are ready to, you can tell us how things are with you. You can ask anything you want, there is no such thing as a silly question, and no judgement here.
Ray.
hope it’s ok I am here…
It’s great that you are. There are lots of helpful and encouraging survivors and thrivers here. Whereabouts in the world are you?
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Hi we’re all happy to help. I’m Hazel 7 years post treatment right palentine tonsil HPV with 7 lymph nodes. Living a great life now.
Good luck with 2 nd appointment
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
Hi PP
Welcome to our community.
This time last year I was diagnosed HPV+ left tonsil and lymph nodes. Similar to you.
Have come through treatment early this year and now life is generally back to normal, but it was a tough journey in the months post treatment.
So, here to help and advise if needed.
Best wishes and do stay in touch.
MickyC
I was told by the surgeon that I was a great Tors candidate followed by radiation. However the radiology oncologist told me this morning that the tumor board discussed my case yesterday and felt it would be in my best interest to skip surgery and go straight to radiation. They want to avoid the triple effects that come from surgery, radiation, and chemo... I admit, as frightened as I was about surgery, I was somehow less frightened than of the radiation and chemo. Doctor did his best to encourage me stating the surgeon who biopsies the site last week pretty much got all the tumor since it was so small - what we are dealing with is the lymph nodes now and whatever microscopic cancer cells remain in my left palatine tonsil area. That he didn't think my qol would suffer a lot....
I meet with MSK next week - and he actually seemed happy I am going there. (He completed his residency there, but moved here because of his family.)
Somehow I find I'm feeling more lost in all of this than yesterday. Was surgery a good thing now off the table? Is radiation/chemo better?
Thanks!
Would like to hear how things went for you as you traveled down the road. If you care to share - I believe I’m open to private messages now
Hi again.
Would be happy to share. Have sent connect request if you would care to connect.
MickyC
Somehow I find I'm feeling more lost in all of this than yesterday. Was surgery a good thing now off the table? Is radiation/chemo better?
I couldn’t have surgery which would have resulted in huge life changing consequences. I had six weeks of RT and nearly seven years later I’m fit and well.
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
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