I have finished my course of chemo for bladder cancer which had spread to glands. I am getting the results of my CT Scan today with the Oncologist. I may well be a candidate for Immunotherapy. Is anyone going through this or been through this? Would like to know how you got on.
Hi LB230, good luck with your meeting.
I had neoadjuvant chemo, Gem/Cis, 4 cycles, then robotic cystectomy (no spread found) then the Oncologist put me on to Nivolumab. I had 3 months of infusions but it caused peripheral neuropathy and so we stopped it so that if the cancer did come back she has options for further treatment. I then had a month and a half of steroids to damp down the p.n.
Now after 2 years my feet and fingers are mostly fine (important because I have a stoma so need to be quite dextrous for that). I do find that sometimes the feet get sore and may not always feel the floor well - important so as not to fall - but I keep up my daily fast walking and use walking poles in case I need stability and to give me an upper body workout at the same time.
I'm not on any formal exercise programme but what I do (and have done for years pre and post bladder cancer) is as least as much as the stuff they are talking about in the papers this week re bowel cancer patients, which is very pleasing.
Hope that helps, any questions happy to help if I can
All the best,
Latestart
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