🔔 Update on access to Zoladex treatment
We heard your concerns about AstraZeneca's decision to discontinue Zoladex 3.6mg from 1 November 2026 - and we went to work on your behalf. After coordinating advocacy with clinicians, consumers and key stakeholders, we're pleased to share that options will be available for those affected, including a free access program for eligible patients and work underway on alternative treatment pathways. Supply continues in the meantime and we'll keep you informed every step of the way. Full details available through the link in our bio. If you need support, our Helpline is here for you on 👉 Reach out to the BCNA Helpline 1800 500 258 for information and support Read more here: 🔗 https://www.bcna.org.au/latest-news/bcna-news/update-on-access-to-zoladex-treatment
Zoladex 3 monthly available but not PBS covered for women
I wanted to share something I recently learned as it might help ease the burden of regular monthly injections. I recently learned that the goserelin injections many of us have monthly are actually available in a 3 monthly dose (10.8mg). I was a really hopeful thinking this could significantly reduce the stress, time and cost that comes with needing to have an injection every 4 weeks. However, my Med Onc informed me that in Australia, the PBS doesn't subsidise the 3 monthly dose for women, although it does for men (prostate cancer). The reasoning given that there's `insufficient evidence of reliable suppression of serum oestradiol' in women. What doesn't make sense is that there is evidence suggesting otherwise. Recent research indicates that the 3 monthly dose is non-inferior to the monthly dose for pre-menopausal women with breast cancer in terms of ovarian suppression. For me, the monthly injections come with a real burden: financially - GP visits and medication add up every month time wise - frequent GP appointments and pharmacy trips take time out of the week. physically and emotionally - injection itself is painful, it's a large slow release implant into the abdominal subcutaneous tissue. The main alternative - surgical removal of the ovaries is obviously much more invasive and comes with it's own risks and long term consequences. Given that the 3 monthly option is already in use, clinically tested and could ease the burden for many of us, I would really like to see equal PBS access for women. I'm curious, has anyone else looked into this and how to go about taking action?
Ode to ovaries
Hello all I’m Nelly ., so I’m new here newly diagnosed and although some may think it’s a bit ‘out there’ I thought I share my latest creation. I call it ode to ovaries as I’ve just started zoladex and entreating the menopause stage at 42 I think it’s beautiful and honouring and it warms me to create this type of work.. I found all the materials on my walks and now it sits in the corner of my bedroom. I do love ritual and I guess it’s me processing positively and honouring my body and journey. I loved making this x
Zoladex
Hi guys just wondering everyones experience with zoladex? I’ve been on it for a month and last three days i just can’t stop crying.. I have arthritis in my neck and that’s been the worst it’s been in a long time for last 10 days and I’m just not sure if it’s the drug or the fact I’ve been running on adrenaline and working hard with horses to keep me busy after op and radiation etc for 3 months and finally just hit a hole... I think I’m die to start tamoxifen soon as well ... Off to oncologist tomorrow for 2nd injection and will also talk to him but just wondering what people have experienced. Thanks 😊
DIEP recon and Zoladex
Has anyone been on Zoladex injections before there DIEP surgery... where did you continue the injections in the month before and after surgery? Were you able to use Lupron instead? I am not a candidate for oopherectomy at my age, but my team can’t give me an answer yet about Zoladex injections. Surely I’m not the only young hormone positive BC patients on zoladex who has gone through DIEP....
