Meet the Other Phone. Only the apps you allow.

Meet the Other Phone.
Only the apps you allow.

Buy now

Please or to access all these features

Cancer

Find advice & support if you or someone you know has been diagnosed with cancer

Colon cancer CAPOX

30 replies

littlebilliie · 05/09/2025 19:36

Has anyone had Oxaliplatin and capecitabine?

OP posts:
Sbmpp · 31/01/2026 22:57

@littlebilliie It took around two months for the neuropathy to resolve from the oxiliplatin. After a few months or so I was started on taxol and it came back. My treatment now is palliative so I guess it will always be a part of my life 🤷🏻‍♀️😵‍💫.

littlebilliie · 01/02/2026 00:28

Sbmpp · 31/01/2026 22:57

@littlebilliie It took around two months for the neuropathy to resolve from the oxiliplatin. After a few months or so I was started on taxol and it came back. My treatment now is palliative so I guess it will always be a part of my life 🤷🏻‍♀️😵‍💫.

I’m sorry to hear this

OP posts:
NewUserName2244 · 01/02/2026 06:32

littlebilliie · 31/01/2026 21:52

Hi all thanks for all
your messages I finished treatment in December nd I’m still feeling neuropathy in my feet and it’s a bit depressing. Any cheerful stories are welcome

I finished capox just before Christmas too and the doctor recommended I take some b12 supplements to see if that helped clear up the neuropathy. Might be worth giving that a go?

gototogo · 01/02/2026 07:21

Thermal inner gloves and tog rated socks are your friends. I have raynauds so this is my life. The silk inner gloves have pads so you can use your phone and I buy boots a size or two bigger to wear extra socks. I have electric heated gloves for the motorcycle 2 sizes bigger so I can wear sink inner gloves and merino wool ones underneath. Unfortunately this all came on in my 40’s and is unlikely to go away, it does look odd to other people when I’m wearing gloves inside or at 15 degrees c

Remaker · 02/02/2026 01:15

Nobody told me that the side effect from chemo would continue to get worse for a couple of months after I finished treatment! When I asked they said oh that’s normal. Mine started to improve after 8 weeks or so. I’m now 2.5 years post treatment and my neuropathy is still improving. I’d kind of accepted whatever I had after a year would be my life forever but it has got less and less over time. As a PP mentioned I’m having my B12 levels checked as that can have an impact too - another thing nobody warned me about!

New posts on this thread. Refresh page