It was a year ago today that I received the phone call from my ENT consultant to give me ‘The news I didn’t want to have to give you’ - that the biopsy on the lump in my neck had revealed squamous cell carcinoma. ‘Probably tonsillar in origin.’ Over the following 18 weeks I underwent scans, more biopsies, a tonsillectomy with neck dissection and six weeks of chemoradiation. My recovery began in the new year.
A year after that first telephone call I’m still recovering and life is getting pretty much as back to as normal as I think it’s ever going to be. My team are pleased with my progress and say that ‘there is currently no sign of residual or recurrent disease’. My neck has improved vastly, although it’s still stiff and tender at times, as has my throat which still appears to change almost daily depending on what and how much I eat and drink. However, there is no pain and eating is nearly normal, although lack of saliva makes some things, like bread, a challenge to get down. My taste has returned, pretty much.
Mentally this thing has been a bit like the Sword of Damocles hanging over my head, but most of the time I’ve been able to push it towards the back of my mind. I know the prognosis is promising but there are always plenty of ‘what if’ moments that never let me forget the cursed thing - a slight toothache, a lump in my throat, a blister on my tongue etc. That said I do count myself lucky to be in the position that I am.
I know lots of you in here are starting or are part-way through this journey. My advice is to use the folk in here as much as you need to and to have faith in your team.
I wish you all the very best with your treatment and recovery. It won’t be worry-free and it won’t be painless but it is manageable.
M
Hi Mark
yep remember your early post s. Don’t give u hope i m almost 3 years and still getting improvements in the saliva department. The current thinking in the u s a I’d now 5 years so bags of time for you. At the one year mark bread was hard for me but now I can eat most breads including baking my own once again.
Only spicy things defeat me now plus alcohol but wasn’t a drinker before so no loss there.
Onwards n upwards
Hazel xc
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
Well done proud of you happy anniversary a year you've never forget and like myself in a pandemic which didn't help but we've done it best wishes x
Mark well done on getting to that first anniversary. Sage words from you about the treatment and how you have reacted to it. I don't think any of us ever fully let our guard down against this cancer, but over time I feel we get to know our new normal better and when to raise the flag for a detailed check.
Now to look forward to that next anniversary, and all the subsequent ones. You've got this cracked :-)
Hi Mark, today is my one year post treatment anniversary for SCC left neck lymph node, unknown primary. Feeling really well except for some long term side effects which are slowly improving. The “what if’s” are always there particularly having CUP, it’s a dark cloud hanging over me, but I’m now realising that I can sit here worrying about the “what if’s” which might never come so I’m not going to waste any more time worrying about something I’ve no control over and I’m now looking forward and planning breaks away. Next month we’ve booked 4 nights at a country house hotel with full Spa facilities, something I dreamed of throughout my treatment. Currently I’m in a hotel room in Wales where I’ve come for a few days so I can visit my mum in her Care Home. We saw each other today, the first time since December 2019 and it was a wonderful teary reunion. So here’s to your 1 year anniversary and my 1 year anniversary, may we both have many more ahead of us.
Best Wishes
Carol
Hi carol
you enjoy your spa break. Hope you’re mums ok and the tears were tears of joy as well.
well done on one year, yes look forwards and not back wards.
Like you say don’t worry over things you’ve no control over it’s a good thought to keep in your mind.
Onwards and upwards
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
Congratulations to you too Carol. I’m glad things are gradually improving for you too and hope you enjoy your well-deserved break!
I’ve just passed my three years when I found my tongue cancer. I’d completely forgotten the anniversary till I saw your post. So it’s possible to be nearly back to normal if you can forget that!
One minute I’m enjoying life and feeling ok for a 67 year old and the next minute I’ve found a lump on the back of my tongue, I know what it is instantly and the following weeks to official diagnosis are just passing time. I wanted the ground to swallow me up and be done with there and then.
But the mind and body are remarkably resilient. So you and I can share a month of discovery if two years apart and enjoy life again.
Well done Mark for a lovey encouraging post
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Hi Carol it's great when we hit those anniversaries - especially in our rather exclusive sub-club of this club
It is also amazing how those side effects slowly disappear and then, all of a sudden, you are left wondering if they really were there in the first place!
Glad you're getting away. Make the most of the life we have and so glad you can visit your Mum; so special for both of you.
Whatever cancer throws your way, we’re right there with you.
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