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Posted 2021-09-20T08:16:00Z

Chemo round 1 is done and dusted!

I’m a quarter way through the first treatment regime! Getting the actual medication today was the easy part. The worst part was getting the cannula access. Due to the mastectomy, I’m only allowed to use my left arm for cannulas. Apparently, my cubital fossa veins (for my nurso friends) need to be saved for emergency use so they had to use the back of my hand. 

Today I requested to have a Port-a-Cath inserted. My nurse and I agreed I just don’t have enough veins for weekly blood tests and regular chemo for the next five months. This is a surgical procedure that will likely be done next week at national capital private hospital. 

For those who want a definition:

“A port-a-cath is used to give intravenous fluids, blood transfusions, chemotherapy, and other drugs. It is also used for taking blood samples. A port-a-cath may stay in place for a long time and helps reduce the need for repeated needle sticks”

Each treatment day will be spent in the hospital and takes anywhere between three and five hours. The hospital has a great set up and I’m confident in the nursing team. I’ve got plenty of reading (and texting) to do during the hospital visit to keep me busy. The chemo will take a few days before the side effects really start to kick-in. There are two weeks in between treatments to allow my body to recover. For now, I still have my hair, but Chris will be cutting it shorter this week.

I left the hospital at around 2pm feeling quite well but have been home a couple of hours now and am starting to feel a bit dizzy, dazed, and nauseated. Let’s hope that doesn’t get any worse. It kind of feels like being pregnant again. I don’t feel like moving around and I’m feeling a bit sea sick. 

Chris has been busy with the kids at home. They have settled into a routine and as we come into the warmer months, there’s plenty of outdoor activities to keep them busy (especially Chris’s tree-climbing).

Next dose in 2 weeks!

Finally, thanks to everyone for your ongoing love and support. We really can’t explain how lovely it has been knowing you have all been right there behind us. I wish we could thank every one of you more. 

 

Love Kirby

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Comments (9)

  • Morgan-Leigh Dawson
    Morgan-Leigh Dawson

    Thanks for the update Kirby. Sending lots of love x

    4 years ago · Reply
  • Chantal Ellis
    Chantal Ellis

    You're a superstar, Kirbs. So proud of you. Hope you feel better soon and we can have our Netflix marathon xxx

    4 years ago · Reply
  • Daz & Lou
    Daz & Lou

    You are one strong lady Kirby - sending you lots of hugs and thinking of you 💗 stay strong and hope to see you all soon xx Lou & Daz xx

    4 years ago · Reply
  • Kerry Mitchell
    Kerry Mitchell

    Thinking of you all ❤️❤️

    4 years ago · Reply
  • Myka Whitchurch
    Myka Whitchurch

    Thinking of you all and sending positive vibes

    4 years ago · Reply
  • Kristine Corker
    Kristine Corker

    Thanks for sharing this Kirby I often think of you and was wondering when you will be starting your treatment. So glad you are getting a porta_cath. Are you taking Zofran or maxalon for your nausea? Praying that your you get through this without too much of the negative symptoms that come with Chemo. Stay bright and cheerful as you are. x

    4 years ago · Reply
  • Jess Warren
    Jess Warren

    So proud of you babe!!!!! Love to you all from all of us xxx

    4 years ago · Reply
  • Fiona Wrench
    Fiona Wrench

    Glad to hear so far not too bad. Hope it stays that way! Kev had a port-a-cath put in yesterday. Take care. Sending our love to you all. XX

    4 years ago · Reply
  • Julie Kapeller
    Julie Kapeller

    Sorry to hear you’ve been having this battle. Best wishes and loads of love to you and your lovely family. Love from the Kapeller family.

    4 years ago · Reply