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Help Kate Fight Multiple Myeloma

  • Update message from Kate and Mike

      29 November 2025

    We're off to Shanghai Dec 10. Unfortunately meds/chemo haven’t worked (including the 11 $5,000 shots) I’m not able to have a stem cell transplant as my bone marrow is 80-90% myeloma. We have spoken to 5 people who've had car t in Shanghai and met with 2 of them. Car-T is a transplant thing where they take my T cells (from white blood cells), genetically engineer them in a lab to create antigens that target cancer cells and then infuse them back into me. It would be at least 7 weeks in Shanghai (around 3-4 weeks in hospital)

    I’ll spend 4 nights/ 5 days at Renji hospital having tests - bloods (30 vials), lung capacity test, ultrasound, bone marrow biopsy, ECG, PET scan, and having my T cells harvested (apparently around 5 hours and I get to drink a lot of liquid calcium) Then we spend anywhere from 4 to 7 days playing tourists (while T cells are being played around with) At Li Quan hospital on day 1 get to do bloods, ECG, ultrasound of heart and a CT scan then a PICC line is put in. Then there’s 3 days of chemo followed by a day off. On day 5 my Car T cells will be infused and following that I have to stay in hospital for 2 weeks. Most people just have a light fever. 3 days after discharge I have to go back for more blood tests (this could change as I am a non- secretor so myeloma doesn’t show in my blood). Day 30 from infusion I go back to the hospital for a bone marrow biopsy. Timings can all change depending on side effects and if I need more than one car t infusion.

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  • To my superheroes

      11 August 2025
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    To my superheroes,

    It has been an incredibly busy few weeks - a CT scan to find causes of pain (multiple fractures of ribs), then a thorough dental check up (we’re talking over an hour and a half) before starting biophosphonate via IV to strengthen my bones. Had first transfusion Aug 7 so I must have great teeth!

    I started doing my own chemotherapy (Bortezomib) shots at home on July 30 - easy as!

    Had my third bone marrow biopsy on Aug 4, this is the only way they can see how/if the initial treatment has worked (usually a blood test is done) sometimes it’s not fun being unusual.

    I had my first dose of Daratumumab (sounds like it should be a Harry Potter spell and costs as much as a small car) on Aug 5. Your kindness, generosity and outright awesomeness has helped me access this life-changing drug

    Then on Aug 8th an MRI of spine and pelvis, we’re waiting to hear what the results are. In the meantime I’m responding to numerous alarms set throughout the day reminding me to take certain meds.

    To everyone who donated to, or shared my page, or donated blood, or sent good vibes and messages: thank you from the bottom of my chemically saturated body.

    This is a long road and having an army of superheroes behind me is vital - because if I stop, I know you’d all keep going (making it necessary to get up in order not to be squashed) so I won’t stop!

    With love and so, so much gratitude, we can not thank you enough,

    Mike, Kate, Saffiyah and Rourke

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  • Thank you all

      24 July 2025

    Thank you all so very much for donating, sharing this page, donating blood and for all the kind and thoughtful messages! We have been so blown away by all your support and we appreciate all of you.

    Kate and Mike are busy with appointments, tests and background research. They will post an update soon.

    For ease of booking to donate blood (if you can) check out the NZ blood donation app.

    https://www.nzblood.co.nz/knowledge-hub/nzbs-donor-app/

    Xx Brigitte

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