Resource Library

"When I was first diagnosed, this tool helped me figure out what I actually needed to know right now, without getting overwhelmed by everything at once."

"I've called this line at 2am when the anxiety hits, and it's such a relief to talk to someone who understands cancer and can help me find resources."

"This booklet helped me understand that living with MBC isn't just about treatment—it's about the practical stuff too, like managing side effects day-to-day and finding emotional support when I need it."

"Having a breast care nurse who actually understands metastatic disease has been life-changing—they're my lifeline when I have questions or just need someone who gets it."

"It's so comforting to connect with other women over 50 who understand what it's like to balance MBC with this stage of life—we just get each other."

"Having a psychologist-led group means I can talk about the hard stuff in a safe space with other women who truly understand what I'm going through."

"When I was told I had brain mets, I was terrified—this resource explained what it meant and what treatments were available in a way I could understand."

"After living with MBC for a while, I wanted to use my experience to help improve research—this course gave me the confidence to become a consumer representative."

"I was nervous about clinical trials, but this video explained them clearly and helped me understand why they might be a good option for me."

"Hearing health professionals discuss brain metastases and quality of life helped me understand that treatment isn't just about survival—it's about living well."

"This comic was the perfect way to explain to my kids what's happening with mum's cancer without scaring them—they could understand it in their own language."

"This gave me clear, reliable Australian information about what metastatic breast cancer actually is and helped me understand my diagnosis without the medical jargon."

"This dictionary helped me understand what my oncologist was saying in appointments so I could actually participate in decisions about my care."

"Learning about biomarkers helped me advocate for genomic testing and opened up treatment options I didn't even know existed."

"Finding resources specifically for triple negative helped me understand why my treatment plan is different and connected me with others navigating the same subtype."

"Watching experts discuss the latest treatments for different subtypes helped me prepare better questions for my oncologist about my own care plan."

"This quick reference guide was perfect when I was newly diagnosed and drowning in information—it pointed me to exactly what I needed without overwhelming me."

"This conference covered everything from medical updates to intimacy and lifestyle—it reminded me that thriving with MBC is possible, not just surviving."

"The Alliance brings together so many organizations working on MBC—it's reassuring to see this level of collaboration and advocacy for people like me."

"As a man with breast cancer, I felt so alone until I heard this podcast—it's reassuring to know there are others navigating this too."

"This site helped me understand what clinical trials are available in Australia and whether I might be eligible for any of them."

"Canteen gave my teenage daughter a space to talk about how my cancer affects her with other young people who understand—she needed that connection."

"This resource helped my partner understand their rights as a carer and find financial support—it's not just about me, they need support too."

"Hearing other First Nations women talk about leaning on community and culture during cancer reminded me of the strength I can draw from my own connections."

"In those first overwhelming weeks after diagnosis, this webinar walked me through what to expect and who would be on my care team."

"This UK charity's focus on secondary breast cancer research and patient stories gave me hope that more people are working to improve our outcomes."

"Hearing from Professor Jacinta Elston, an Aboriginal woman who's been through this, helped me understand how to navigate the healthcare system while staying connected to my culture."

"This podcast feels like having conversations with friends who truly get it—hearing other people's stories helps me feel less alone on the hard days."

"This resource helped me understand my rights to cultural safety during treatment and gave me the language to ask for what I need."

"Having a virtual wellness house means I can connect with support and wellness activities from home, even when I'm not feeling well enough to go out."

"My kids are taking on so much helping me—this network gave them support and showed them they're not alone in caring for a parent with cancer."

"Being able to translate the website into my preferred language means I can access all the information without language being a barrier."

"This database helped me search for trials myself and come to appointments prepared to discuss options with my oncologist."

"Having information in my mother's language meant she could finally understand what's happening with my cancer and feel more involved in supporting me."

"This podcast series helped me understand how genomics is changing cancer treatment and why precision medicine might be relevant for my care."

"Understanding what all those scans—CT, PET, bone scan—actually do and why I need them helped reduce my anxiety about the diagnostic process."

"When I see questionable health information online, I use this tool to check if it's actually true—it helps me feel confident about what I'm reading."

"I shared this with my care team to help them understand the specific challenges LGBTIQ+ people face in palliative care—it's about being seen and respected."

"This site helped me understand my employment rights and gave me language to discuss flexible work arrangements with my employer while managing treatment."

"This alliance is working to make sure men with breast cancer aren't forgotten in research and treatment—it's validating to see advocacy specifically for us."

"These translated resources helped my whole family understand metastatic breast cancer, not just those of us who speak English fluently."

"Having a list of questions ready for my appointment meant I didn't forget to ask important things when my brain was foggy from shock."

"Being diagnosed young means facing unique challenges—So Brave connects me with other young women navigating career, family planning, and cancer all at once."

"As a man with breast cancer, finding this monthly Zoom group was huge—finally, others who understand what it's like to have a 'women's disease.'"

"This US organization's resources for young women with breast cancer helped me feel less alone in dealing with fertility, dating, and career concerns alongside cancer."

"Having a free, professionally facilitated weekly group funded by Queensland Health means I can access quality support without financial stress."

"As a WA local, having access to breast care nurses, counselling, and practical assistance right here has been essential—they understand the unique challenges of living in Perth."

"Knowing there's active breast cancer research happening in WA gives me hope and helps me understand the latest treatment advances available here."

"Cancer Council's trusted, evidence-based information gave me a reliable starting point when I was overwhelmed by conflicting information online."

"This comprehensive guide is my go-to reference for everything MBC—I keep coming back to it at different stages of my journey when I need detailed information."

"Being under 50 with breast cancer brings different challenges—this group gets what it's like to balance young kids, careers, and cancer."

"Living in Newcastle, HBCF's practical help with transport, cleaning, and yard maintenance has been a lifeline when I'm too exhausted from treatment."

"It's such a relief to have a private space to talk about intimacy struggles with cancer—topics that feel too awkward to discuss elsewhere."

"Listening to practical advice from others living with MBC while I'm doing chemo or resting helps me feel connected and informed."

"Connecting with other women over 50 with metastatic disease means we can talk about the unique challenges of dealing with MBC at this life stage."

"The free complementary therapies and support programs at Solaris help me manage side effects and stress without adding financial burden."

"Learning about palliative care early helped me understand it's not just about end-of-life—it's about symptom management and quality of life at any stage."

"The Living Centre in Melbourne offers psychological, emotional, and practical support all in one place—it's become my wellness hub."

"The weekly therapeutic group for metastatic patients, and the partner group, means both my husband and I have support from others who truly understand."

"ASCO's resources helped me understand treatment options that might not be available in Australia yet, which I could discuss with my oncologist."

"Cancer Chicks gets what it's like to be a young woman dealing with cancer—the community here understands the unique struggles we face."

"Counterpart's peer support service connected me with another woman living with cancer who gets what I'm going through—having that connection matters."

"As a doctor with cancer myself, this group provides unique peer support from others who understand both sides of the medical experience."

"When my oncologist mentioned ESMO guidelines, I looked them up to better understand the international standards guiding my care."

"This clinical guideline database helped me understand the Australian standard of care and whether my treatment aligns with current best practice."

"The annual public lecture keeps me updated on the latest research in a way that's accessible to patients, not just medical professionals."

"This app made it so much easier to coordinate help from friends and family—people want to help but often don't know how."

"I was curious about integrative treatment approaches—this resource helped me understand different philosophies, though I checked everything with my oncologist first."

"This book helped me understand how nutrition and metabolic health might support my conventional treatment, giving me practical things I can do."

"Hearing survivor stories and learning about factors that might support healing gave me hope and ideas for supporting my own wellbeing."

"Watching these educational videos for health professionals helps me understand what my oncologist is considering and ask more informed questions."

"This extensive collection of articles and podcasts helps me stay informed about different treatment approaches and complementary therapies."

"This private group connects me with others who have TNBC and understand the specific challenges and treatment options for our subtype."

"The free wellness programs and retreat space at BRICC give me somewhere peaceful to relax and recharge between treatments."

"When I was considering complementary practitioners, AHPRA helped me verify qualifications and make sure they were properly registered and regulated."

"BCNA's information on breast cancer types and subtypes helped me understand exactly what my specific diagnosis means and why it matters for treatment."

"When breast cancer spread to my brain, this organization provided patient-focused information and advocacy specifically for brain tumour issues."

"When I developed brain metastases, this resource helped me understand what was happening and what treatment options might be available."

"Cancer Australia's MBC-specific page gave me authoritative Australian information I could trust when I was trying to understand my diagnosis."

"Canteen's support specifically for young people aged 12-25 impacted by cancer meant my teenage kids could get age-appropriate help dealing with my diagnosis."

"Hearing from a breast surgeon who became a breast cancer patient herself brings such a unique and honest perspective that resonates with me."

"Exercise oncology specialists understand how to help me stay active safely during treatment—they know cancer and exercise, not just generic fitness."

"This comprehensive handbook from Canada covers everything about MBC in one place—I refer back to it whenever I have questions about my diagnosis."

"Reading about Stage 4 symptoms and seeing survivor stories helped me understand that metastatic doesn't mean giving up—people are living with this."

"The holistic support at this WA centre—from counselling to complementary therapies—helps me manage the emotional and physical toll of cancer."