Dear all,
Here i am finished my treatment on Friday and I can’t explain how happy i am
how was my experience????
hm, after my second chemo i was poorly as i was very nauseous all the way to the end. I lost kg a lot, and I can’t eat as much… no appetite as you know, but drinking… i can swallow and still on cocdamol, but a lot of spitting which is so uncomfortable
I am tired, but thats normal and my skin on my neck is red and with pilling skin, for now…
So, hopefully will stay like that!
i am not sure what to expect as everyone said next week can be very painful so, hopefully not.
thinking of Helen! Hope all is going well!
good luck all
love from Marta x
Ah Marta! Yay, you've done it! Congratulations
It sounds like the chemo was rough - I felt very nauseous after my 1st cisplatin for almost a week. I have my 2nd (and last) chemo on Monday ... I'm dreading it, but at least I know what to expect. So far I'm still eating/ swallowing. But I can't taste anything, which has affected my appetite of course. The Fortisip drinks will be very useful in the next few weeks I think.
I'm getting the Radio fatigue - I sleep very well these days, up to 10 hours
I had a RIG inserted last week (my hospital trust insits on the tube). It was very painful but slowly getting better and if I need it then I can get a lot of calories very easily. I haven't used it so far, just practiced with water, but it it's pretty easy.
My neck is red but not peeling. I'm using the Propolis cream (I hate the smell but it works like magic!). My mouth got sore in week 1 & 2 but felt better last week as I stopped using Duraphat toothpaste so often, just at night, it was burning my mouth, awful stuff!
I miss the taste of real food SO much.... I had lasagna tonight with veg and coleslaw - but they all tasted exactly the same LOL!!
I'll be following how your progress goes, keep us posted xxx
So good to hear from you!
i think i was nauseous even with tablets against it.. grrr
Specially after driving
i asked oncologist and he ask me not to use anything he doesn’t know as we don’t know what is happening with radiotherapy.
Anyway, i can use it now
Milkshakes are ok, but they make me even more mucus yuk
good luck with all!
will be in touch x
i am not sure what to expect as everyone said next week can be very painfu
Hi Marta, well done.
The two/three weeks after treatment ends can be challenging as the radiotherapy has a residual effect for that long but in my experience and that of many others here the pain isn't any worse. For me things plateaued around four weeks and stayed there. I think, for me it was the disappointment that I wasn't going to get better straight away. Time to sleep and heal.
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
I miss the taste of real food SO much.... I had lasagna tonight with veg and coleslaw - but they all tasted exactly the same LOL!!
Heavens! I am impressed. By end of week three I was using my NG tuber exclusively.
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Hi Marta well done and just hunker down for next 2-3 weeks , as Dani says the pain stabilise but you need to recover. This article might help it helped me and many others
I spent the first 2 weeks feeding oral hygiene sleeping then start again with the same.
You’ll get there we all do some quicker than others it’s not a sprint it’s a marathon.
At least no more daily hospital visits.
Hazel xx
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,
My mum's been an inpatient since last Friday, got NG on Wednesday and RIG on Friday, but due to finish her radiotherapy on Tuesday and cannot wait until we don't have to visit the hospital anymore. Hoping for discharge on Tuesday so she can ring that bell after RT and come straight home.
She only managed 3/6 of the planned Cisplatins, hoping this won't effect overall results.
Planning for her to be quite sore/tired over the next week or so, how long do you think before her mouth will begin to feel a bit better?
She only managed 3/6 of the planned Cisplatins, hoping this won't effect overall results.
Planning for her to be quite sore/tired over the next week or so, how long do you think before her mouth will begin to feel a bit better?
Hi. Missing chemo doesn’t matter too much so don’t worry.
Looking at what other folk on here report most of us feel quite a bit better by six weeks and turn a real corner at twelve.
It can take months for taste to return and for saliva to become less problematic
Have a read of this excellent article to psychologist Dr Peter Harvey. It talks about recovery after cancer. It’s very useful. I printed out a few copies and handed them out to friends and family
www.workingwithcancer.co.uk/.../After-the-treatment-finishes-then-what.pdf
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
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