💬 Access to treatment matters - an update on Tucatinib
Right now, hundreds of Australian women with HER-2 positive breast cancer are stuck in limbo, denied affordable access to a life-extending drug, Tucatinib. Tucatinib has been approved for listing on the Pharmaceutical Benefits Scheme (PBS) by our own government, and is easily available for women in other countries. Despite the urgency, negotiations between Pfizer and the Australian Government have stalled, denying Australian women affordable access, and they're running out of time. It’s a trend we’re seeing more often with other drugs and health concerns: delay tactics from big pharmaceutical companies and lack of leadership from the Australian Government. All the while, it’s the patients who suffer. We won’t stop fighting for these women to live a better quality of life and have more time with their families while they still can. Vicki Durston, BCNA’s Director of Policy, Advocacy and Support Services, explains how our system is failing women with metastatic breast cancer and that we must address the growing threat to medicine access caused by big pharma stalemates. Read more about this and how it affects Australians like Georgie Cooper, 46 years old with 3 teenagers living in Melbourne who has been navigating metastatic breast cancer for eight years.🩷1 week until Pink Bun is back!🫓
Just one week left until our 2026 Pink Bun Campaign kicks off with Bakers Delight! 🎉 From 14 – 27 May, buy a pink Fun Bun 6 Pack from your nearest Bakers Delight, 100% of sales go to BCNA so we can continue supporting all Australians affected by breast cancer 🩷 more details coming soon.... 👀Wach this space!🎉🏃♀️Celebrating Sarah’s incredible marathon milestone!
We love sharing moments of strength, joy, and achievement from within our community, and today we are celebrating some truly wonderful news from Sarah, one of our Consumer Representatives. This week, Sarah completed the London Marathon, an extraordinary achievement at any time, and even more remarkable while living with metastatic breast cancer. Covering 40 kilometres through some of London’s most iconic sights, Sarah described the day as “big” in every sense. From Big Ben to the Tower Bridge and a powerful finish down The Mall, it was a marathon filled with determination, challenge, and unforgettable moments. Like many long distance runners, Sarah experienced highs and lows along the course. She started strong, slowed to soak up the atmosphere, and faced the infamous wall later in the race. With grit and resolve, she regrouped, kept moving forward, and finished strong, supported by the cheers of the crowd and the encouragement of loved ones along the way. What makes this milestone especially meaningful is the reflection Sarah shared afterwards. For the first time, she embraced that being “awesome” is not about times or performance, but about showing up, persevering, and doing something extraordinary simply by being there. Only a small percentage of people ever complete a marathon. Fewer still complete more than one. And the number of people who have completed 13 marathons while living with metastatic breast cancer is incredibly small. That makes this achievement not just impressive, but deeply inspiring. Sarah also shared how powerful it was to see the stories of others running for loved ones, causes, and personal reasons. A reminder of how sport, movement, and community can connect us and lift us up in unexpected ways. We are so grateful to Sarah for being willing to share her experience with our community. Stories like this remind us that there is no one way to live with metastatic breast cancer, and that moments of strength, pride, and joy still matter. 💪 Congratulations Sarah!
Policy & Advocacy Update - Vicki Durston - Apr26
Hi everyone, I hope you are doing well today. I wanted to share some reflections with our Online Network community, because many of the issues we are hearing about right now go to the heart of why this community exists. Thank you for being here, for supporting one another, and for continuing to lend your voices to the changes that are so urgently needed. This is about access, advocacy, and what happens when the system does not move fast enough for the people depending on it. Access delayed is access denied 🕰️ Australians deserve a Pharmaceutical Benefits Scheme that delivers timely, affordable access to life saving medicines. It is one of the foundations of our health system, and something Australians trust to be there when it matters most. Right now, that trust is being tested. Women living with metastatic breast cancer still cannot access tucatinib, an evidence based therapy for HER2 positive brain metastases. The Pharmaceutical Benefits Advisory Committee recommended tucatinib for PBS listing in December 2025. Despite this, negotiations between the Australian Government and Pfizer have stalled on price, leaving the medication unaffordable at $64,000-$70,000 for treatment. This is more than an administrative delay. It represents a breakdown in the system. For women with metastatic breast cancer, time is not a policy concept. Disease progresses. Treatment options narrow. Time with loved ones disappears. When neither government nor industry moves, it is women who carry the consequences. As highlighted recently in The Australian, BCNA is raising awareness about what this failure means for women with metastatic breast cancer. This is not just about one medicine. Allowing PBAC recommended therapies to stall indefinitely risks setting a dangerous precedent that could undermine timely access to future medicines across many disease areas. The reality of metastatic breast cancer 🎗️ People living with metastatic breast cancer continue to tell us that the public conversation does not reflect their reality. While pink ribbons, survivorship and positivity have their place, they do not capture what it means to live with incurable disease. As Dr Ilana Galgut has shared, many people with metastatic breast cancer feel the pressure to present a version of themselves that feels palatable to others, while carrying the ongoing reality of scans, progression and uncertainty. People are living longer, but longer does not mean easier. It means ongoing treatment, constant monitoring, fear of progression, and for some, devastation when disease spreads to the brain. This is where awareness must move beyond storytelling. When women courageously make themselves visible, the system must respond with urgency, fairness and access to treatment. It is not acceptable to ask people to share their truth while access to medicines like tucatinib collapses quietly behind closed doors. Modern treatments need modern care models 🏥 Cancer treatment has changed, but too often our models of care have not kept pace. Today, more Australians are receiving oral cancer therapies at home. For many, this reduces time in hospital and improves quality of life. But oral treatments can be dangerously underestimated. Too often, taking a tablet is treated as predictable and low risk. Yet questions remain unanswered. Who monitors adherence? Who manages toxicity? Who identifies early deterioration? Who intervenes before someone presents to emergency? We are hearing directly from nurses, nurse practitioners and oncologists who are calling for care to be reimagined. Nurse led clinics, electronic patient reported outcomes, digital monitoring, urgent symptom clinics, specialist telehealth and improved navigation pathways all exist. The challenge is not innovation. It is whether the system is willing to listen and act. With MASCC coming to Melbourne in June, one of the world’s only major conferences dedicated entirely to supportive cancer care, we urge those working in cancer care, research and policy to engage deeply with the global evidence and consider how change can be implemented locally. When advocacy works ✨ Amid these challenges, it is important to acknowledge what sustained advocacy can achieve. Australia has now passed landmark legislation banning genetic discrimination in life insurance. This reform means people can access genetic testing without fear that results will be used against them when seeking life insurance. This change did not happen quickly. It followed more than a decade of determined advocacy led by Dr Jane Tiller and Krystal Barter, supported by researchers, organisations and advocates across the country, including BCNA. It is a powerful reminder that even when progress feels slow, persistence matters. For women at risk of breast cancer, this reform removes a significant and unfair barrier. It creates greater confidence to access information that can influence prevention, early intervention and life changing decisions. Where we stand now 💬 Advocacy is not abstract. It is deeply human. It is about ensuring women living with metastatic breast cancer are not left waiting while negotiations stall. It is about designing care systems that support people receiving treatment at home. It is about removing barriers that never should have existed. BCNA is calling on our community, clinicians, researchers, leaders and decision makers to stand with us and demand urgent access to tucatinib. For women with metastatic breast cancer, delays are not theoretical. They are measured in time women do not have. Australians deserve better, and together, we will keep pushing for a system that delivers when it matters most 💙💊Advocacy Update: Standing Strong for Access to Tucatinib
We wanted to share an important update on BCNA’s advocacy for tucatinib, a targeted therapy used to treat HER2‑positive metastatic breast cancer. 📍 Where things currently stand While tucatinib has received a positive PBAC recommendation, talks to secure its listing on the PBS have stalled, particularly around pricing between the Australian Government and Pfizer. In the meantime, the current cost to patients is around $64,000, creating significant financial barriers and uncertainty for those who need it. 🔥 Advocacy momentum is building Momentum in BCNA’s advocacy continues to build, with strong media engagement helping to raise awareness, including an article in The Australian, coordinated activity across BCNA’s Instagram, Facebook and LinkedIn channels, and a radio interview on ABC Melbourne. Each of these moments helps keep tucatinib access firmly on the public and policy agenda. 🤝 What comes next Behind the scenes, we are actively progressing advocacy with both government and Pfizer, and a number of potential pathways are being explored to address this. We remain focused on keeping pressure on Pfizer and decision-makers while also identifying any interim options. We’ll continue to keep you informed as things progress and will reach out if there are any specific actions we’d like your support with.🎉A Landmark Win: Australia Bans Genetic Discrimination in Life Insurance!
Declared today - what a start to the month! After ten years of sustained advocacy, Australia has passed legislation banning genetic discrimination in life insurance. This is a historic moment for fairness, medicine, and genomic health. 🧬The bill has now passed the Senate and will become enforceable in October 2026, giving insurers time to update their systems. Once active, Australians will finally be able to access genetic testing without worrying about how their results might affect life insurance 🎉 💙 This reform follows years of work from advocates including our very own Vicki Durston, and Monash University’s Dr Jane Tiller who described the outcome as extraordinary and vital for protecting everyday Australians. It also creates new opportunities for preventive genomic screening through programs like DNA Screen, which has already provided life‑saving information to participants. 🌺 Stories like that of 22‑year‑old Mia Hodder, who carries a BRCA2 variant, show the real impact of this shift. She shared that genetic testing empowered her to take preventive action and expressed relief that others will now be protected from discrimination when making similar choices. 🎊This legislation marks a major step forward for public health, early detection, and equitable access to genetic information. A huge victory for medicine, for genomics, and for fairness. More updates will follow as the implementation date approaches, if you're interested in learning more, you can read the Monash University media release here.📣 BCNA's Strategy 2025–2030 Now Available
We are absolutely thrilled to share something truly special with you - Breast Cancer Network Australia's Strategy 2025–2030 is officially available to view and it marks a bold, inspiring new chapter for all Australians affected by breast cancer. This strategy isn’t just a document. It's a promise to be louder, braver, and more determined than ever in driving change. Built from the voices, experiences, and hopes of people all across our community, this roadmap sets out the ambitious work ahead - from strengthening advocacy and pushing for equity in care, to elevating lived experience so every voice is heard where it matters most. ✨ It reflects where we’ve been. It celebrates where we are. And it charts a powerful path for where we’re going, together. You can read the full strategy here: 👉 https://www.bcna.org.au/media/l5ua3c3e/bcna-strategy-2025-2030.pdf We’d love to know: What excites you most? What sparks hope or inspiration? Your insights continue to shape everything we do, and this moment is very much yours. Thank you for being at the heart of our community - your courage, honesty, and support drive the work ahead. Here’s to five years of impact, connection, and meaningful change. 💗💪Join us in welcoming Gabrielle Coyne as our new Board Chair👏🎉
After 10 years as Chair of the BCNA Board - we are bidding a grateful farewell to Kathryn Fagg AC. Kathryn’s leadership has been transformative. Powered by her own breast cancer diagnosis in 2012, she didn’t just lead our Board; she championed our community. Under her guidance, BCNA has: 👉 Delivered quality information and support to millions of Australians 👉 Built ways to connect those with lived experience together 👉 Secured PBS listings for many lifesaving and life-prolonging drugs like Enhertu and Keytruda. 👉 Launched the landmark 'State of the Nation' report to bridge gaps in care. 👉 Secured $1.5M in federal funding to ensure metastatic breast cancer patients are finally counted. Kathryn, your inspiring spirit has changed the landscape of breast cancer support in Australia. We are also proud to welcome Gabrielle Coyne as our new Board Chair. With Gabrielle's extensive experience and shared passion, we are ready to continue our work of ensuring all Australians affected by breast cancer receive the information, care and support they need.🌟 BCNA's 2025 Impact Report Is Here!
What a year it was. In 2025, BCNA reached further, stood louder, and showed up stronger in the places where we’re needed most. From the sparkling shores of Bondi to the heart of Willetton, our community carried us into conversations, fundraisers, gatherings, and moments that truly mattered. We didn’t just raise awareness, we raised voices, hope, connection, and the courage to keep going. And none of it could have happened without you. 💗 At BCNA, everything starts with care for our community. Every story, every milestone, every ripple of change begins with the individuals who make up this extraordinary community. This year’s Impact Report isn’t just numbers - it’s a living, breathing celebration of the people behind them. The women, men, and families who opened their hearts, shared their experiences, and reminded us why this work matters so deeply. We’ve gathered some of our favourite stories from the past year - stories of strength, innovation, resilience, and community spirit that carried us forward. Take a moment to explore them. Let them inspire you. Let them remind you of the difference we make together. 💕Here’s to another year of impact, connection, and hope. Thank you for being part of this incredible community - for standing with us, walking with us, and believing in what we can achieve together. 👉Read BCNA's 2025 Impact Report Here
CEO Update - Kirsten Pilatti - Mar26
Hi everyone, Every year, International Women’s Day gives us a moment to pause, reflect, and recommit to creating a more equitable world. This year’s UN Women Australia theme “Balance the Scales” resonates deeply with the work we do at BCNA and with the lived experiences of the hundreds of thousands of women we serve. Recently, I had the privilege of spending time with our long-time partner Sussan to explore what this year’s theme truly means for women navigating Australia’s healthcare system. Their guiding motto “By Women, For Women” pairs powerfully with “Balance the Scales”, highlighting both the strength of women supporting women and the urgency of creating systems that work with them, not against them. In our conversation, I reflected on how often women must fight to be heard, believed, and supported within a healthcare landscape that was never designed with them in mind. At BCNA, our Purpose is to stand for all Australians affected by breast cancer. We want to ensure that everyone can access the care, dignity, and understanding they deserve. 👉 Watch the video here ✨ Our 2025–2030 Strategy: Putting lived experience at the centre For more than 25 years, BCNA has fought to ensure that women's lived experience isn’t an afterthought, it’s the blueprint for action. Our new five-year strategy strengthens this commitment. It sets a bold direction to ensure our: support is stronger advocacy is louder reach is wider impact is deeper ❤️ I believe that the people we serve are the heartbeat of our organisation. This strategy represents their voices, their stories, and their needs. 👉 Explore the 2025–2030 Strategy ✨ Looking back to look forward One of the stories that continues to inspire me is that of our founder, Lyn Swinburne. In the year 2000, Lyn – mum, teacher, and fierce advocate – sat inside the Élysée Palace in Paris. Pen in hand, she paused for a moment, smiling nervously, before signing an international Charter in the presence of French President Jacques Chirac. That moment was more than ceremonial. It marked the beginning of BCNA’s enduring commitment to global advocacy, to women’s rights in healthcare, and to building a future where equity isn’t aspirational, it’s expected. 👉Read more here
