Hi
I had my diagnosis a week into lockdown last year - it was a huge shock. I had surgery in May and now have a permanent stoma. I had 3 months of Capox chemo which I wasn't too keen on!
I've just had the all clear from a CT scan and finished chemo last September. Due to Covid there have been no support services and most of my consunltant appointments have been over the phone.
I've stayed positive throughout and almost better now - just surprised how long the neuropathy & tiredness has lasted after chemo.
If anyone would like support going through similar treatment, I'd love to help support you. I'd also like to chat to people about the after effects of chemo as the hospital have told me very little.
Looking forward to chatting with you.
Nina x
