Hi all - newly diagnosed and due to start chemo radiotherapy shortly. Stage 3 non small cell lung cancer. The chemotherapy is ‘all day’. Anyone else having this, and how long is all day. I will have continuous radiotherapy from third session onwards, daily for 5 weeks. I will also be taking chemo tablets. Any advice, information or coping mechanisms would be very welcome. Just a little bit overwhelmed by it all. Thanks for your time. Sending everyone hugs.
Hi Kettlechip
I too have stage 3 nsclc spread to lymph nodes in centre of chest, underwent 3 cycles of chemo and 6 weeks of radiotherapy, My chemo took all day which was about 6 hours when getting my 2 chemo treatments it is a long day so take book/kindle to read something to drink and some nibbles. There’s always people to talk too so sometimes can go quite quick. I didn’t cope to well with the sickness ended up in hospital for a few days but everyone is different think half my problem was dehydration so remember and drink plenty of fluids . I could only eat small meals bought a lot ready made ones and pots of custard and rice pudding. It’s not going to be easy, but we get there. I’m on immunotherapy now for a year so far so good tumour shrinking and my next check is December.
Big hugs
I also had full days during my chemo treatments, as Evelyns says about 6 hours. This was because you need to be on a saline drip before administration of the chemo (mine was cisplatin) and then on a saline drip again after administration to flush your system and prevent kidney damage. Each saline course alone takes up to an hour from memory.
You will doubtless be told that you need to be alert to possible infections during treatment as it affects the immune system and I was recommended to get a thermometer and check temperature daily as a precaution, I didn't have a problem though and most do not either, it's just a case of being aware. Also take all the meds they give you even if you don't feel bad as these will also help head off any problems. Then take things at your own pace and don't overdo things, if you feel tired rest, and eat what you feel like but try to get plenty of calories. Finally based on experience I suggest if you get side effects like mouth ulcers or constipation ask the hospital or your GP for something to deal with this, don't waste your money on over the counter products at the chemist, I found they didn't work well at all.
I hope your treatment goes well and is a complete success.
Evelyns, thanks for taking the time to come back to me. Taken your advice on board re hydration and small meals. Already stockpiling bits and pieces. Obviously at the moment I don’t know how I’ll be with side effects, but I’m sure I’ll take it on the chin! Wishing you all good luck and all the best with your future. Big hugs
Hi excavator. Again, thanks for taking the time to come back to me. I’m now more on board about meals and keeping hydrated etc and as the chemo days are long I’ll be taking books/magazines/snacks and iPad. Due to visit the chemo ward soon and I’ll take on board their advice too. Just good to reach out to other lovelies in the same boat. Take care and good luck.
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2025 © 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