Oxaliplatin & capcetabine

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Hi, wanted to connect with those currently having this type of Chemo; on to my second cycle of 8. I appear unwell 5 days post chemo but start to feel better day 6 so far; anyone else experience this?

 Not sure how my side effects compare to others:

Pain & tingling in infusion site, face, nose, pain on chewing first two bites normallyI'm 

Nausea

tiredness,im menopausal & have terrible sweats & insomnia directly after treatment; might be the steroids?

It helps to know how others are dealing with things?

  • Thank you so much for the advice, glad i joined!

  • Best of luck, its tough going so support from others who understand is greatBlush

  • Thank you, its tough but can't go anywhere or do anything because of covid so lets get our head down & keep going!Kissing heart

  • Thats great news for you!Blush well done for getting through it!

  • Thanks so much for your advice, thats really helpful!Blush

  • Hi, Im only one cycle in front of you, i'm having 8 cycles which feels like a marathon! Its tough at the beginning isn't it when its all stretching ahead of you; and the anxiety of covid! I'm trying not to look too far ahead, its hard though when your not feeling well. I'm on day 7 of 2nd cycle; feel better today but it appears days 1-6 are pretty rubbish. I suppose once we've had a few cycles we will be more prepared; its scarey stuff dealing with unpredictable symptoms take care keep going xx

  • Former Member
    Former Member

    Hi Rosiegirl . Hope you are doing better today . I have just finished my 3rd cycle of Capox .  First and second cycle  pre Christmas I was absolutely frozen, quite a lot of pain in the infusion arm and around the cannula.   Bad Peripheral neuropathy .. so could not touch anything for 5/6 days .All the doors handles in my house were wearing socks permanently ;-)  Felt dreadful - zero energy and absolutely no ability to go outside as I could not handle the cold.  Following a discussion with the oncologist  he reduced the oxaliplatin dose by 20% . It made an incredible difference . Still felt the cold - but the hand tingling only lasted 24 hours .  For the first 5/6 days I still needed to sleep in the afternoon - but thereafter so , so much better. 

    It also helped a lot to ensure that you were warm going into your appointment  and to use a heat pad on the arm where  you are getting the infusion before  and during. 

    Hope things get better for you. 

  • Hi Nelly B I had chemo tablets with the radiation after first scams in December they thought most of the cancer had gone. Had to have another scan on the 6 of January went last 13 and it was gone. They will have me back in 3 months. I just want to ask my doctor about diet to try and keep as well as I can. Love & kindness to us all x

  • I'm on my third cycle of the same, I've had similar symptoms plus laryngeal spasm after each infusion, so from an initial 2hr infusion my 3rd was over 4 hours. But things do improve slowly. In my chemotherapy free week I feel almost normal. The reset when I start a new cycle is unpleasant, but I  take comfort from the knowledge that thungs do improve. Unfortunately, because of COVID19 delays I'm having 4 cycles before my review of progress, so it will be longer than expected before i find out if the treatment is helping.

    But to look on the positive side, nearly every day one to day 21 of the cycle has been a little better than the day before

    Sarah 

  • Thank you for your response, i took the advice of buying cotton gloves & wearing them at all times in the house, even for sleeping keeps hands at a constant temperatureThumbsupkeep going! Sending good vibes!