Happy New Year to you all.
I have been discharged by my oncologist, handed over to the ENT team. She confirmed there was no sign of cancer in my tonsil and lymph nodes. Started treatment 3rd July.
I did need a colonoscopy due to some activity showing up on the PET scan which was a bit alarming but turned out to be a polyp with no cell changes phew. So for anyone whose PET scan picks up activity it’s not always what you automatically think.
I'm 4.5 months post treatment eating well with the help of water, sauces and lashings of gravy. I’ve been eating out for the past 2 months albeit it a limited selection but that is increasing. I now like my beef rare find it’s easier to swallow, strangely I thought fish would be easy to eat but I find it very dry maybe need to try sushi Lol.
I’m giving acupuncture a go to try and increase saliva production only 2 sessions in can’t say it’s working yet but will keep you posted.
For anyone starting your journey there is light at the end of the tunnel but it can be a bumpy ride.
Hi BAM23 that's great news. You will find things will continue to improve, for a good while to come, I'm over 6 years post treatment, and I'm still getting slight improvements. Like you say, posts like this, show others that you can come through this with good results. Best wishes for the New Year.
Ray.
Thanks for posting your good news. It’s a slow road to recovery but things get better and better.
I too had an avid PET which threw me mightily but biopsy was benign.
Have a great 2024
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
I wrote a blog about my cancer. just click on the link below
Hi Bam23 brilliant news I found acupuncture helped kick start my saliva glands but still needed sugar free gum to help stimulate them. 5 years on I get dry mouth in the night but dayme I don’t notice it any more. One life just live it.
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
Thank you, so hoping I can have normal saliva once again.
Hi You will do I remember thinking would mg mouth ever feel normal again. It almost normal I never imagined in that first year or 2 it would but I no longer think about it in the daytime.
we all get there in the end just takes time.
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
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