I had my regular check up today (palpating and nasoscope) with my very thorough and attentive surgeon, and all was well. However, I’m just a bit puzzled as to why I’m still on two-monthly checks coming up to two years post treatment. I reported feeling absolutely fine and having no major issues and was told that it all ‘looked lovely’ in there. I’ll now get a phone consultation in two months and a face to face two months after that. My team have always been very honest with me and have my absolute trust, but it’s bugging me a bit as people in here seem to go down to just three monthly checks in year 2. Or maybe I should just be grateful that they are being so thorough by seeing me more frequently? Or maybe different hospitals have different protocols?
I had every six weeks for six months then two months in first two years. That went up to every three months in the third year now I’m every six months. I’m shared between Maxfac and oncology. So I see Maxfac once more and oncologist twice then I’m done. All my transitions have been a couple of months late
I wouldn’t read anything into the way you are monitored.
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 Mike. I no how you feel iam every 4 weeks ..it does set alarm bells ringing. Thanks for people on here we can sleep easier..best of luck for the future
Doesn’t it just! Are you new here? If so I hope your treatment is going smoothly.
No i be on here for about 4 mouths. I had cancer inside the nose ..had tumour removed in may..and yes everything is fine so far thanks for asking..everyone on here are great dani and hazel and a lot more ..great talkin to you.
Yes. Hazel and Dani et al are priceless and this forum is invaluable at times like this. Glad you’re getting on well.
HinAs the others have said don’t stress about it all hospitals have different protocols. I was every 6 weeks to start with then it gradually went to every 3 months in year 2/3 with covid then appearing I went onto phone calls but still seen if I needed ti be seen in between. Sometimes I’ve had ti chase my appointments up I’m down to last 2 with ent now on every 6 months and last one with oncologist. But have already been told once the 5 years is up i can still make direct contact with medical secretary rather than back to g p and be put back in the system it’s reassuring to know that.
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
Yes. Hazel and Dani et al are priceless
Flattery will get you anywhere
Mark you can include yourself. Your profile diary is brilliant and I tell lots of people to read it.
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
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2024 © 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: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007