I finished radiotherapy to the oesophagus in the middle of September. For the last 2 weeks of treatment eating hot more and more painful. I have tried various painkilling formulas with little success and I also have near constant nausea and constipation.
I was thinking things should be getting a bit better now,5 weeks post treatment, but they aren't. Eating and drinking burns and even liquid oxycodene is painful to take.
Has anyone had a similar experience and able to offer advice?
Thanks
Hi,
Im sorry to hear your tumour has returned.
Have you seen a consultant regarding the reoccurrence of your tumour? As they should dicuss your next pathway. Did you have chemotherapy prior to radiotherapy?
My dad finished his radiotherapy in October and has just started 2nd line treatment of Paclitaxel in January.
Kayleigh
Thanks Kayleigh,I'm seeing the Oncologist this week but have constant conact with GI nurses who are very helpful. I just wanted other folks experiences as obviously I'm wondering what comes next. I had some chemo but had to stop as I got sepsis and I had radiotherapy too but reacted badly and in any case I can't have radiotherapy in the same place. I hope your Dad is progressing well?
Thanks Lozza, it's all so confusing at times isn't it? I had almost given up hope when I posted that but have since been assured by my MacMillan GI nurse that they won't just abandon me. So I'll see what the Oncologist has to say this week. As I just said to Kayleigh, I reacted badly to both chemo and radiotherapy,so yes,I think I'm right to be worried. x
It is confusing. Absolutely. Why couldn't you have surgery? Radiotherapy was never discussed as an option for Rod. They mentioned it as a possibility if his tumour was bleeding but that hasn't been identified as the cause of his low bloods afterall.
Today the oncologist said to him that fitting the stent and draining the fluid that filled his abdomen last week is all they can do now, unless he can start eating and get stronger to have chemo. 4 litres came out in the 1st 2 hours! He was virtually begging to have the fluid drained by Friday but was told it couldn't be done until today. Hence, increasing strengths and doses of morphine.
I'm relieved for you at the response from the GI nurse.
Take care,
Lorraine x
I can understand your worry. As that's we all just do isnt it, especially when a treatment doesn't work. I do hope you get some answers and get steered in the right direction.
Dad is doing well at the moment thank you. We have another dreaded scan on the 30th March, hate waiting for those results.
He is due to see his oncologist next week and he will be speaking with him regarding his pain in his leg, apparently this is a side effect to paclitaxel.
We just take each day as it comes.
I wish you all the best.
Kayleigh
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