Hi to all.
Ive been lurking in the background on this forum for a while since diagnosis, having a read on everyone’s journey.
Now it’s my time,
I’ve just returned home after my first infusion (Oxaliplatin).
The idea of me writing this is is no different to others before me, as some have said “it’s good to talk” (old BT ad I think).
I had my infusion whilst having my feet and hands in a Hilotherm machine which the nurses at QE Woolwich were keen for me to try, as I speak it clearly helps, as my right hand which had the cannula in and couldn’t have the cooling glove on is very sensitive to cold (why is it when someone tells you don,t touch cold things as it’s going hurt, we do) or maybe just me then.
By way of my back story, for those who maybe in a similar boat.
I am stage 4 upper rectal cancer which has spread to the liver, I’m on a CAPOX treatment of 8 cycles with Neo-adjuvant intent.
I will be reporting back with side effects etc. hopefully with the aim of helping others in a similar predicament and of others posting their thoughts as well.
For those who may read this and not return, Merry Christmas and a Happy New Year, for those who intend to return see you soon.
