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Just diagnosed
Hi, I thought I would introduce myself here. I am 49 years old and have just been diagnosed (two days ago) with an Invasive Ductal Carcinoma in my left breast. HR+ HER 2 negative, provisional grade 1, 4 small lumps. Will be meeting my surgeon at RBWH next week on Wednesday. The last 11 days, since the Breast screen recall feel like a blur. So much has happened and of course I didn’t anticipate any of that (lumps aren’t palpable). I have been directed here by the wonderful nurse from the Breast Screen and am very grateful to find so much support and information. I haven’t told my kids or friends yet so it feels good to be able to open up here.
Waiting, waiting, waiting….
Hi all, diagnosed 1st September, multifocal invasive lobular carcinoma. Surgeons appt scheduled for 17 September. Surgeon has referred me for an mri with contrast. The surgeon completed my biopsies (3) in breast screen clinic, so I’ve met her. My biggest question now is how long do you wait for the mri apointment? They acknowledge receipt of ‘urgent referral’ on 2nd of September and now it’s the 10th, they’re telling me they are waiting on ‘protocols’, my breast care nurse is wonderful and is following it up along with me, how long did you all wait? I thought I was coping not too bad, but today it all just seems really cruel……?
Very difficult to listen the Podcast
Hi all, so I started listening to Charlotte's podcast. I just started the Episode 2. While this podcast is fantastic, I find it extremely hard to listen and my emotions just overcome me. I would love to know how is everyone going and what do you do to stay calm and not be a slobbering and emotional mess like me. 😔 Thank you everyone 💓
DCIS diagnosis last friday
I found out Friday afternoon that I had DCIS, thought nothing of it till later in the evening when I was doing a bit of research . Totally overwhelmed & unsure what to do now, surgeon is having a team meeting Wednesday & then having a telehealth with me. AtM I’m trying to put together a few questions based on the pathology results I have. I want to be proactive & aggressive in confronting this disease. Any commments or ideas? I have had MRI, needle biopsy, ultrasounds, & then excision. This was all following my sister diagnosis of invasive lobular breast cancer recently. I had no symptoms prior & a negative mammogram last November .First appointment with a surgeon
So my first appointment with a surgeon is this coming Wednesday. I am going through a public system in Brisbane. Will I be having any tests done on the same day or is it more likely that he will tell me to come back and get the tests done another day ? He’s got my mammogram, ultrasound and biopsy results already. Thank you!
Radiotherapy
Hello everyone, l am going through my first radiotherapy this week and l was wondering can l take a NSAD prior to my treatment? I have bursitis on my shoulders and, during my mapping l found it so painful trying to lift my arms. I was thinking of neurofen. I would be grateful for any feedback. 🌸Discussion about surgery with Surgeon
Hi all, I have been diagnosed with invasive breast cancer and I have my first meeting with the surgeon on Thursday. I know to expect surgery soon but dont know if this will be lumpectomy or mastectomy. I know that this will be one of the things to discuss on Thursday but I am curious if there is a 'choice' - in a sense part of me just wants to be told which option but I wondered if anyone here made a decision one way or the other and how they felt about that? Am also putting this query in the treatment thread as I have not posted before and not sure which is better for this. Thanks for any thoughts.
Triple Positive HER2+
Hi everyone BCNA Online Network established a Group with Triple Positive breast cancer which is useful also for people who might be HER2+ but not positive for oestrogen or progesterone. This post is also to alert previously accepted Triple Positive Group members: you might not have been automatically transferred across to the Triple Positive Group with the recent upgrade to the new BCNA Network site. Please do request to rejoin the Group (I did)! Ned01CheriSukiCheriAnna15FeRnurserachMareealsoTriplebreast240Number2CaitySXC1947
Newly diagnosed
Hi all, I have received a diagnosis of DCIS, I was told on Friday, and now I need another biopsy before we work out the best way forward, obviously the two options are mastectomy or lumpectomy, my concern is I can’t have this other biopsy for 3weeks, I feel overwhelmed, I was also diagnosed with Multiple Sclerosis this time last year, and I am a hairdresser, so I’m finding work a struggle and I’m wondering what I should expect with the recovery if I have a mastectomy and reconstruction vs lumpectomy and radiation? I would love to hear if anyone has experience any restrictions as a hairdresser getting back to work after a mastectomy? After my MS diagnosis I had to cut my business in half because of fatigue, now I’m concerned that I won’t have a business left after this if I can’t work for a while 😢Feeling lost
I am newly diagnosed and just feel lost. My appointments and tests have been so close to each other. I have had mammogram, ultrasound, biopsy of the breast, FNA of my lymph node, a pet scan and having a mri tomorrow. My diagnosis is invasive carcinoma NST (invasive ductal carcinoma), grade 3, triple-positive (ER+/PR+/HER2+), with associated high-grade DCIS. The ki-67 is 60%. I have been told the I will have 4 months of Chemo, then surgery, radiation and long term medication after. I met with the breastcare nurse and found her extremely unhelpful. I just don’t know what to expect and how to feel at the moment. Has anyone been on a similar journey who can tell me what to expect?