Newbie…long story
Hi everyone, Newbie here. Never dreamt I would be joining this club, but who does ?! This forum and website have been so helpful to me over the past month. My journey started last June when I decided to speak with my GP about a tender spot right on the inside edge of my left breast. She reassured me that tenderness isn’t typically a symptom of breast cancer, but we would check it out. Got an ultrasound and mammogram. US identified a small mass, mammo some calcifications. Got an us biopsy around October, all clear. Then around Christmas I noticed some brown nipple discharge (took a while to accept it was coming from the nipple, thought I had spilt something…. Every few days in the same spot!!!). Back to the GP, another ultrasound. The report said there was “debris” in the duct, couldn’t exclude papilloma, MRI would confirm, surgical consult recommended. So off for the consult, after which I was told the discharge was due to trauma to the breast from the biopsy (they didn’t send me for the MRI). This was purely based on discussion and very brief examination. In hindsight and knowing what I do now, I would have pushed back and demanded the MRI regardless. Relief! But my GP wasn’t convinced. She sent me for an MRI then a consult with a specialist breast surgeon who, after looking at the MRI, immediately sent me for some MRI and stereotactic biopsies…2 in my left and one in the right. That was a bit of a marathon! I was convinced it was all a waste of time and money! I turned up to the surgeon for results unconcerned…obviously rather naive! “You’ve got a lot going on in your breasts!” were her first words. LCIS and papilloma in my right breast, DCIS and invasive Mucinous carcinoma in my left. I was speechless. Shocked. Bewildered. Confused. We briefly discussed next steps, but I couldn’t get out of there fast enough! I called my husband in tears. We went back together to the surgeon the following Monday, after doing a bit of research, lots of reading, and chatting with a wonderful McGrath Breast Care Nurse. After asking more questions, I decided on a left mastectomy and right lumpectomy. Plus sentinel node biopsy on the left. But I was so angry. How could the first surgeon send me away without really being sure??!! I went through all the feelings, disbelief, anger, sadness, grief, a bit more anger, and finally acceptance (mostly anyway!!). I realise I have to let go of the anger, and am taking it on as a learning - it’s important to advocate for our own health and not accept something too easily if it doesn’t seem right. Hubby and I had a two week holiday booked up north the following week, which the surgeon said was fine, so we booked surgery for August 13, ten days after we would get home. The holiday was great, we hadn’t told anyone at that point (except my mum and work). We were able to not think about it and had some really special time together. It was good to have the space and time to process what was happening. so now I’m one week post surgery, contemplating the future, keen to get back to everything I used to do. I had been training for a half marathon in September, which of course now won’t be happening. We are hiking the Overland Track in February, so that’s what I’m aiming for. I’m so very lucky to have an amazing, competent, supportive partner. He has taken the same time off work as me to support my recovery. He even washed my hair for me yesterday :-) Recovery is going pretty well, although I’m often still uncomfortable in bed. Getting the drain tube out a couple of days ago was wonderful! We go back to the surgeon next week (two weeks after surgery) for dressings etc and results. Fingers and toes are all crossed! Thanks for getting this far, there’s something a little cathartic in writing this down. I’ve really appreciated reading others stories, it helps with knowing we are not alone and the feelings are valid. Thank you :-) Belinda xx
Thankfully I know more this time.
So, 7 and a bit years after a Stage 3 E+ PR+ breast cancer diagnosis in the left breast, I am facing some changes in the right breast. Picked up in yearly mammogram/ultrasound. Nobody has suggested it is cancer just yet but given my history I am booked in for a core biopsy next Monday. I am very clear in my head about what this means for me. I have been happy with my choice of single mastectomy for the last 7 years but am not about to take any chances with the remaining breast. Regardless of the results of the biopsy, it’s days are numbered. Monitoring changes in a very dense breast is not what I want. Having had a mastectomy I am quite ok about having a second one, especially if that is all I need. The changes are new since my mammogram and ultrasound last year. Just goes to show that keeping up our regular checks is sooo important, even in our current Covid 19 world. Very reassured by the excellent treatment of my situation by the staff at the Radiology facility this morning. I was treated respectfully and everything was clearly explained right then and there. As you can imagine though, I am finding it hard to concentrate on anything else at the moment. Will be glad when the biopsy is done and we have the results. But I am sure that a mastectomy is what I want regardless.
Struggling
Hi ladies, away with my family spending some quality time but last 24 hours been so emotional and stressed, was diagnosed with TNBC early Dec, having 4 rounds of chemo, 16 rounds of taxol and then surgery - unsure at this stage what surgery as having genetic testing in a couple of weeks to see if I am a carrier for bracca 1/2. I had my first chemo 31st Dec, all went ok and other than first day where I had severe nausea that night the next 5 days I was just really exhausted - going into my 2nd post treatment i seem to be going ok. The thing is, the last 24 hours there is a burning pain in my tight breast and it’s sore and right arm aches - I had a needle biopsy the day before my chemo as ct showed a lesion in breast node so it is just over a week ago now and the side of my breast got really bruised and where they stuck the anaesthetic to numb the area still feels tingly and swollen, my husband says when he was looking at the ultrasound and needle was going in she was really pushing hard to grab the samples and they stuck 3 needles in to get enough, results came back fine and was benign so was a relief but I am stressing as it’s really sore still- has anyone had similar experiences with biopsies as all I can think is that this terrible diesels has spread even though my Scans mid Dec were clear. also I wonder if chemo is working and I know I am being stupid as I have only had 1 session and everyone is different but reading the side affects like hair falling out before 2nd cycle ( I am having a few strands come out only, more like malting but not much) nails going black, mine are fine at the moment, it’s not like I want these things but physiologically I feel if these things start to happen chemo is working - it’s such a mind f**k. sorry for the long winded post but just needed to release xx
New Blood test (hopefully soon) that does away with biopsy!
This popped up in my news feed this morning - being developed by Queensland University! It seems that cancer DNA binds with gold molecules ..... identifying cancer in the blood with out the need for invasive and painful Biopsies! Abu Sina Research Fellow, The University of Queensland Laura G. Carrascosa Postdoctoral Research Fellow, The University of Queensland Matt Trau Professor, The University of Queensland Hopefully they kick off human trials soon ..... and made available to everyone Read all about it here: https://theconversation.com/one-test-to-diagnose-them-all-researchers-exploit-cancers-unique-dna-signature-108078
Waiting for results
Hi all....happy I found this place to share and learn :) Sooo....I had the re-call after mammogram. No lump as such, just little white area on mammogram. Visit to Breast Clinic for more mammograms and ultrasound. Results showed suspicious 7mm papillery lesion so had 7 core needle biopsies taken. No actual cancerous cells in core biopsies, but as there was also mucin? fluid found with extravasation, which apparently can also be in cancerous lesions, they wanted to take out whole area to be sure. Had surgical biopsy done last Friday, go back for final results on the 31st October. Resting up off work this week and although sore as expected, getting easier each day. Thank goodness I have Netflix! Finding this the hardest part, waiting....wondering which rabbit hole, if any, I’ll be going down next :/
On the roller coaster
Hi everyone. Waiting for my biopsy results. Left breast with one huge 6cm and few smaller ones. Ultrasound showed no lymph nodes affected. So as I’m trying to prepare. I am in NT and would like to know about your breast surgeons etc. I’m thinking of travelling interstate for the surgery. My reason is our public hospital made a huge error with my colleague. The path results showed she had reoccurring bc and they booked her in for mastectomy. Only to find out 2 weeks later there was no bc and she did not need the mastectomy and their pathology made the mistake. So having said that you can imagine my gut is saying no, no to the hospital and all it’s bc staff. If you’re comfortable to share your experience and surgeon info etc, is really appreciate that. Putting it blunt, I don’t have control of the lumps but at least I can have control of choosing the hospital and surgeon. Thanks. Would love to hear your thoughts.
Difficult to organize a biopsy
A week ago I had a CT scan of the chest due to being out of breath. It was thought to be a problem with my lungs though I have no cough and don't smoke. The scan showed a 3.7 cm calcified elongated mass in the right breast tissue. It also showed scattered ground glass densities. Sometimes this can indicate metastatic breast cancer. I've read that a mass that is elongated should be investigated, and 3.7 cm is quite large. As well, both my mother and grandmother had breast cancer after menopause. The type in both cases was slow growing and didn't kill either of them. I asked the GP if I could get a guided needle aspiration biopsy. She gave me a referral. Wouldn't you think such a thing is urgent? I rang the imaging centre where the CT scan was done, in a town a half hour drive away, and they had several weeks' wait. I tried every centre in Canberra and they all had a wait between several weeks and several months. Wouldn't this mean the difference between treatable cancer, and one that has got away to the point that it's terminal? I thought even a week's delay could be dangerous? I finally found a place near Wollongong that can do the biopsy in two weeks' time. I'll need to drive three hours to get there. I'm just horrified that it's so difficult to get a biopsy of a suspicious lump. Has anyone else had this experience?BMX with ALN removal and SN biopsy.
Hello to all you lovely folks on here. I've had 6 cycles of THCP and I'm having BMX this Wednesday, with axillary clearance on the left and sentinal node biopsy on the right. Has anyone had the same? And any advice for recovery? Were you able to go out for a walk or is it mostly housebound at first? I'm also dealing with heamorroids so a little worried about that. Thank you and best wishes to everyone going through this.
2nd operation DCIS
Hi all, Was diagnosed in Feb this year with high grade DCIS, 3 small tumours. Lumpectomy 3 weeks ago. Pathology report came up with not clean edges. The surgeon said I have two options, do another re-excision with most likely radiotherapy and endocrine therapy, or mastectomy. I have a family history of breast cancer. Has anyone been through this desición before? What was your experience like? outcomes? Thanks for sharing
