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Pathology results from surgery
Saw my surgeon today and got my results. He was surprised to find I have two different types of Breast Cancer. I have Stage 1 -mixed ICC in breast and Stage 2 -DCIS in 1st sentinal lymph node. Have an appointment Friday (17th) with the radio. oncologist then 30th March with the medical oncologist. Radioitheraphy is…
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New
New diagnosed, 73, introvert, living alone. Surgery tomorrow (2nd March) for lumpectomy and sentinal lymphnode. My doc has told me I will be having radiontherapy once the biosypy results are in.
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Young Mum
Hello everyone, I'm so grateful for this online community. It's been an overwhelming time for me. I was diagnosed on the 23/12/22 and had a really tough two weeks as I was unable to access any support just being to the time of year it was. I was breastfeeding my 20 month year old at the time, and didn't feel a lump, but…
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Overwhelmed new diagnosis
Just trying to cope with this whirlwind of a ride. Two weeks ago I was happily holidaying on Hamilton Island (the first holiday in three years) and this week I'm isolating at home after a positive Covid test, only to be told that I have Breast Cancer. Surely this week could not get any worse. The surgery, that was…
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Are you a breast cancer survivor who happens to be childless?
I have been a member of this online network since 2014, just after my diagnosis. At a recent breast cancer seminar at a city near where I live, something hit me like it hasn't in all this time, the subject of survivors who happen to be childless. I thought to myself, "Noone talks about this. Why?" This has led me to do my…
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Alone ... finding a surgeon
On the day I was given my biopsy results I was on my own. Apparently, it was the first day in 2022 that patients were allowed a support person when receiving pathology results ....but noone told me. All the signs at Breast Screen Vic stated that support people were asked to wait outside due to Covid. With it being really…
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4 years since BC diagnosis & joining BCNA & my surgery ...
Woohoo! This year was the first year that I didn't actually 'remember' that Jan 5th was the anniversary of my actual diagnosis of BC ...... so that must be a good sign! So - today - it is now 4 years ago since I joined BCNA (at the suggestion of a girlfriend in Qld who had been diagnosed a few years earlier) .... and a few…
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46 / Hi / Comfort of knowing you guys are here /(IVF link?)
Hi all I know this is a weird first post for “Newly Diagnosed”! but Im alone today, the day I got the call, and I literally just wanted to reach out to my sisters who know how I feel. It’s comforting to know you’re out there. Right now I can just say hi. I’m still numb and I can’t bring myself to write the details just…
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Dealing with metastatic breast cancer diagnosis
Original post created by member @Opoho moved to own thread in ‘Metastatic breast cancer’ category:
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First consultation for DCIS - private or public?
I was diagnosed a few weeks ago with low-grade DCIS, showing up in 2 clusters of microcalcifications on my right friedegg. All quite sudden given I'm 42 and was expecting to be chased away from BreastScreen NSW telling me it was cysts, which has happened to me previously. Instead, I got the works (mammo, ultrasound, biopsy…
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Things worth remembering
Ruth Hunt, in Perth, has published a letter to herself, about the things she would have found valuable to know earlier, before metastatic cancer, It seemed to me a really good list for almost anyone. Her circumstances are very sad, but she has found a way of looking at the best of her life. A link to the full letter is at…