So im now five weeks post surgery from the removal of my sigmoid colon due to cancer. I have been informed that the cancer was completely removed , although the histology showed there was cancer was in three of my lympnodes. for this reason Im being refered to oncology to discuss chemotherapy opitons.
Im feeling very nervous at present, even though Im told the chemotherapy is a precaution. I'm after advice from any person who has gone throught the chemotherpy route on what to expect. I understand everyones journey is diiferent, I'm simply looking for some guidance to help quite my mind.
Hi and a warm welcome to the board. Congratulations on now being cancer free and I hope you’re recovering well from the op. Chemo is pretty unpredictable and affects each person differently but, although there can be a lot of side effects, there are also a lot of remedies and actions that can be taken to minimise them.
Yes the chemo is a precaution but personally I wanted to know that I’d done everything in my power to minimise the chance of a reoccurrence. If you decide not to have the chemo and were to have a reoccurrence, would you be able to live with your decision without wondering what if? There was a trial done a few years ago called the SCOT trial which showed that 3 months chemo was just as effective as 6 but with much less side effects.
Ive attached a link below to a post that we have about chemo side effects - hopefully it’s not too scary but just covers some of the main ones
Hope this helps and feel free to ask if there’s anything specific that you’re worried about
Take care
Karen x
Hi Ephm211,
I also had 1 lymph node affected and was offered adjuvant chemotherapy. I was very nervous about having the chemo and was particularly worried about peripheral neuropathy. However, I wanted to do everything I could to give myself the best chance so I agree with both Karen & Gemmary. Although not pleasant, it turned out to be easier than I'd expected.
Let us know which chemo regime you're offered. there are lots of pills and options to help with any side effects and there's lots of advice on here from people who've been there.
Best wishes,
Net77
Hi there
I thought I’d share my thoughts with you. I was told that I may have chemo. Two weeks after the op I was phoned and told it was all out and no chemo needed.
I was delighted that they’d got it all out but then I worried that I didn’t have chemo. My heads all over the place. so go for it.
I hope all goes well.
Ann
After my panproctocolectomy they said none of the 60 nodes tested were affected but gave me the choice of chemo as "belt and braces" I took it as I wanted to throw everything possible at it.
It is a personal choice obviously but one I thought worthwhile.
All the best
Kath
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