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sentinel node biopsy
Hi there my name is Anna. i am having surgery next week , my anxiety levels are pretty high. i am very nervous about the sentinel node biopsy. the idea of having a needle near the nipple. i am reading about it, it doesn't mention having a local injection, like we did with the core needle biopsy. anyone please tell me about your experiencesRadiation Therapy
It's all been very quick diagnosed with stage 1, grade 1 invasive breast cancer, ER+ then appointment with surgeon 2 days later, lumpectomy and removal of two lymph nodes 4 days after seeing surgeon. Currently day 3 after surgery, home recovering. Get results on lymph nodes and margins next week. I'm trying not to think too far ahead, but ... I worry about radiation (been told 5 days a week for 4 weeks) and how it will affect me as I work full-time. Any advise on what I can do to make the next stage of treatment easier and what to expect ☺️Write off 6 to 12 months?
I was given a diagnosis today of small tumor, early invasive breast cancer, double hormone positive and I have an appointment with surgeon in 1 week. At just-turned-60, the next 9 months were supposed to include 2 sons' graduations, 1 son's wedding (a family first), our 25th wedding celebration, a road trip to find-purchase-or-build a new home in a tree-change location in another state, and downsizing-packing-relocating. Surgeon and nurse at breast clinic today seemed to think "we can work around things" ...is that realistic? What is the most valuable question to ask the surgeon, next week, re time frames and realistic expectations? Thanks.Hair Loss Advice
Hi beautiful people. I have just commenced chemo a few weeks ago and I am just starting to lose my hair. I have bought some hats and scarves but I would appreciate some advice on wigs. Looking at the possibility of a real hair wig? Would really appreciate your opinions. I live in the the Wollongong area. Thanks ☺️366Views0likes12CommentsJust need to talk to someone
I’m 59yo and newly diagnosed with breast cancer. I’m really not sure I get what is going on either because I’m just slow or it’s just not all clear yet so I feel confused, in total panic and that I’m drowning and there is nobody to save me 😢 I am waiting for an mri this Thursday. I have a 10cm Not Special Type Grade 1 something positive to do with hormones and her2 1+. The surgeon says mastectomy is the only choice because of the size. There isn’t anything clear about what happens after that… is that how it’s meant to be? I just feel very lost appreciate any words of wisdom for these circumstances? susan326Views0likes15CommentsWorking while waiting for surgery
Hi all, was diagnosed 3 weeks ago today with early stage and was told I’d be having surgery pretty quickly. Ended up having to have more tests to eliminate issues in the other side and thankfully that all seems to be clear. But that has meant I still don’t have a date for surgery (I should find out tomorrow hopefully). My question is about how you’ve all kept sane during this ‘limbo’ period. My emotions and anxiety are all over the place, I can’t really focus or concentrate so I’ve taken a fair few days off work. I’m lucky enough that I can work from home (when I’m up to it) and my boss is awesome but I weirdly feel guilty about taking time off as though I should be managing this better. I’m conscious my surgery might not be for another few weeks so feel I need to work out better ways to handle this. Any inputs welcome! Thanks.My first post
Hello lovely ladies, First time mammogram identified the need for a 3D mammogram, then ultrasound & biopsy in my left breast. All via Breast Screen Victoria. Biopsy showed 18 x 17 x 5mm 'high grade DCIS' (clinical notes on 21/3). As I'm in the public system I'm now waiting on having a MRI. My question though relates to the paperwork saying 'E-Cadherin stain and hormone receptors to follow'. Its been 16 days since the biopsy was reported on. How do I receive or who gives me these 'E-Cadherin stain and hormone receptor' results? Should it be via Breast Screen Victoria? Am I meant to chase them up myself?118Views0likes3CommentsNew grade 1 diagnosis
Hello. I’ve just been diagnosed: left breast invasive ductal, grade 1, hormone receptor-positive, HER2-negative. GP summary is that this is a low-grade hormone-positive breast cancer that can be successfully treated usually with lumpectomy then radiotherapy. I’m seeing a surgeon next week and feel relieved that this has been caught early. That said, I’m not looking forward to the next few months and am wondered if there is anyone else at a similar starting point - or people who’ve been down a similar road and can share advice and support. I’m 59, live in Sydney, work full time in a high pressure job, and am a single mum with a teenager at home. Thank youYoung and overwhelmed
Hi all, I'm 30 years old, with the BRCA 2 gene mutation, and was diagnosed after my first high-risk screening MRI found a tumour - mixed lobular and ductal invasive carcinoma, stage 2, grade 2, hormone receptor positive, HER2 negative. Because of my BRCA status, I had a double mastectomy in February 2026. An 11mm tumor was removed alongside a 50mm DCIS component that was associated with the invasive tumor and adjacent tissue was removed from my left breast, but my right breast was all clear. The sentinel lymph node biopsy showed a 1mm micrometastases in one node (of two). Initially, the plan was just a double mastectomy followed by endocrine therapy, but the option of chemo has been put on the table post-surgery (and even the choice of two different regimes). My oncologist's justification was "we want to give you every option available because you're young" but it feels like I've just been given an impossible decision with no clear better option. I'm also having a lot of anxiety around chemo and the implications for fertility as I am yet to have children (I was able to freeze a small number of eggs pre-surgery but I would have to self-fund any further cycles). I'm not entirely sure why I'm posting this but maybe I'm just hoping someone will have had a similar experience (especially if you were diagnosed young or before having kids!) or have some words of advice because I'm feeling overwhelmed by all of the choices I'm having to make.