Back to page

Julie’s Cancer Journey

  • Next Stage

      30 April 2023

    As these guys are on the way down to Wellington to continue the next phase of this crappy journey!

    If you can please help these guys out if you can, we would 100% appreciate it!

    Ju is one the toughest gals I know and she will give it her all, she already has been and she will continue too.

    Darrell is the bestest big bro in-law one could ask for,

    He’s got julie’s and Callum’s back 100%.

    Callum you got this my nephew you will be there for your mumma 100% and you keep those parents under control we have got your backs guys, see you when this part is over 💗💗

    Cancer we are coming for ya yet again, once again you have picked the wrong family 🤬👊

    Take a hike cancer!!

    Let’s keep trying to help these

    Guys out in what ever way you can.

    Thanks so much for anything that you have done or given or just chats,

    Call ins etc 💗💗

    Travel safe team A 💗💗💗

      0 comments  |  Login to leave a comment
  • The April Update

      15 April 2023
    Posted by: Julie Anderson
    Main image

    Hello Everyone,

    Darrell, Callum and I would like to say a vey big heartfelt thank you for all the support, kindness and generosity we have had since my cancer diagnosis in January. It has been very humbling to feel your wrap around support and all the aroha during this rollercoaster of a journey.

    Currently we are waiting to hear from Wellington to confirm the dates of my next operation. This one is to remove the 10 centimetre cyst on one of my ovaries which was picked up in the CT scan, during the recovery of my double mastectomy. The same CT scan also picked up an oddness in my stomach lining. We wont know if the cyst is benign or if the stomach lining is something to be concerned about until after the operation. There are varied opinions on this. They will take a biopsy of the ‘oddness’ during the operation. If it is cancer, it will mean it’s secondary. This adds a complication to the current treatment plan so it’s important to see what is happening before starting chemo.

    To keep the lobular cancer from regrowing, I have started on tamoxifen. I am feeling bursts of tiredness from it, headaches and a bit of brain fog, but nothing really compared to what I could be experiencing. And I’d rather take it, to prevent anything from developing. I will keep taking this till chemo starts.

    My current treatment plan is:

    Operation - 2nd of May in Wellington. Removal of cysts, ovary, tube and biopsy of stomach lining.

    Chemo - in New Plymouth 2/3 weeks after the operation. Once every 3 weeks for 6 months.

    Radio - In Palmerston North for 3 weeks, 5 days a week

    Tamoxifen for 5 years.

    This will depend on what the operation finds.Otherwise we re looking at a very different situation.

    We will keep you updated, but just wanted to say a big thank you to you all. The Tū mannaki (kindness) we have been shown is just so touching. We can not thank you enough. Thank you for all the prayers, baking, donations thoughts and hugs. Everything has given us courage that we are not alone in this.

    A special thank you today to my friend Mel who has set up a fundraiser to shave her hair, in support of when I start losing mine. I’m just lost for words Mel - your friendship is everything to me.

    At the start of 2023 I picked a word for the year, Tū kaha. (Courage) When I picked it, which was more to do with the staff going surfing as a team building event, I did not realise that Tū kaha would be the word I would need for the entire year of 2023!

    It seems to perfectly fit for this journey.

    Thank you so much everyone.

    We will update you!

    You are all wonderful!

    Julie, Darrell and Callum.

      0 comments  |  Login to leave a comment