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Help Holly fight Stage 4 Cancer

  • Amazing news!

      13 March 2025
    Posted by: Holly Norman
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    I’m so proud to share that I’m now in remission!

    My last CT scan has shown no evidence of disease (NED) and that the remaining mass is likely fibrosis (scar tissue) - whoohoo!

    I’ve been given the all clear to stop immunotherapy (funded Keytruda) after 26 rounds. I will need to continue taking my BRAF inhibitors for improve my chances of a durable remission - now $14,700 per month (until I reach the cap of $70,000).

    I’m feeling immensely thankful to be part of the small percentage of people who can say they’re NED with stage 4. Looking forward to regaining a sense of normality to life and as always forever grateful for your continued support X

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  • Goal adjustment

      13 November 2024

    Hi team,

    We are endlessly grateful for the generosity that the community has shown to support Holly. We have however had to readjust the current goal due to an increase in medical costs. Here are a few of the reasons as to why we are needing the extra support.

    As Holly moves towards self-funding her medication and accessing required medical equipment we realised that our initial goal was not sufficient.

    Additional Costs:

    -Anticancer drugs have increased from $8800 per month to $13,500 per month.

    -Access to a Lymphoedema specialist

    -The purchase of the LF900 Compression pump at $2700

    -Any other unexpected costs

    Thank you once again,

    with love

    Cait x

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  • Thank you!

      24 October 2024
    Posted by: Holly Norman

    A huge thank you from me and my Mum! Your donations have allowed me access to valuable resources that wouldn't have been attainable otherwise.

    - I've been seeing a private Melanoma Specialist who has given us a clear plan moving forward and has provided us with something even more valuable; lots of hope!

    - I've been able to visit a Lymphedema therapist and purchase new compression garments to combat the complications caused by my initial surgeries.

    My last few scans have shown my disease is stable which is a huge win! I'm having minimal side effects from treatment and have now reached the 1 year mark on Keytruda - 1 more year to go. One day at a time! <3

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  • QR code

      9 August 2024
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    Hi Team, a few of you had asked for ways in which you could help out. If you could please share these posters around. Feel free to print a few out and pop them in to your locals; cafes, shops etc the QR will lead you to this page. Every little bit of help takes us a step further so thank you so much 😊

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  • Holly’s 15th round of immunotherapy

      25 July 2024
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    Hi Everyone we wanted to update you on Holly’s challenging journey. She has just had her 15th round of immunotherapy where she also received her next round of daily targeted therapy. She is such a trooper. While these times are very challenging she is giving it her all.

    She’s back home now with her dear cat Milly Mouse to rest up after a busy week.

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