Hello everyone. I have had just received the news that a second set of biopsies under mammography (really wasn't prepared for that prolonged hour long, painful ordeal!) have also shown DCIS as expected. This area was 3.5 cm away from the first clusters if calcium... a total of 5 small areas. I have a hospital appointment on Monday with the breast surgeon. My mind has gone into overdrive and I wake early, as another lady stated, thinking BREAST CANCER! I thought I would be brave, and feel angry with myself as I'm lucky it's just DCIS not other kinds. Could be worse. I am wondering if a 3.5cm area would mean lumpectomy, or as others have indicated when it's over an area they have had mastectomy? I know it will be up to the surgeon but feel I need to be prepared for that as a possibility..... It is so frightening.
Have others just accepted that "shit happens"? Because I'm really struggling with the why? How? My lifestyle is such that I exercise every day, am still slim, eat incredibly healthily, don't drink much, have never smoked, no family history..... is it HRT, recent STRESS? my driven personality? I know people say it's not always lifestyle, children can get it, but I'm reeling from my immune system having allowed this to happen. I know I have to get in a positive frame of mind, I'm just not getting there yet. Please help. I'm struggling.
Hi Kimost. My post surgery bra is a bit more industrial. It does up at the front as some have said it’s difficult to reach around to do a bra up at the back post surgery. It also reduces the amount my boobs jiggle. I’ve found that any car journeys can be a bit painful since my biopsy, in fact anything that makes me jiggle. Hubby has been advised to drive me back from hospital slowly and avoiding little lanes with potholes.
Chickenlover that is so true. Any bump in the road would make me moan in pain for weeks after the surgery! All ok now though. It is my 39week pregmant daughter who groans at bumps in the road now lol
Thanks. All my sports bras are underwired so not suitable. I shall go shopping this weekend.
I had the radioactive seeding. It was really awful. It took an hour and 45 minutes as they couldn't find the 2 metal clips placed during the 2 biopsies. I had to have the seeds planted under mammography and again they couldn't get the position right. My calcifications are at the very back near the chest wall. It took 2 nurses pulling my breast and clamping my ribs to be able to target the area. I'm in bed feeling sorry for myself. I'm grateful for their persistence and one particular nurse held my hand. The radiographer himself was lacking empathy. He seemed totally oblivious to my pain... saying things like slight sting!!! Or "discomfo"!!! I wanted to stamp on his balls and call it discomfort! Sorry to rant but it was truly horrid.
So sorry, it sounds like you have had a horrible time having the mag seed inserted. It is in and awaiting surgery now though so try to relax and tell yourself you have got through that stage and it is on to the next one. You can pick them off and be proud of yourself each time you get through each one on the way to getting you better.
Definitely don't apologise for the rant. It will help you to get it off your chest (apologies no pun inyended) and out there and we are here to listen.
Hi Kimost , that sounds awful! I’m so sorry I would have wanted to stamp on his balls too. Sometimes it just feels like one assault after another. I had the covid swab and another blood test yesterday, tiny little things but it’s getting to the point where I just want to be left alone.
op tomorrow, thank goodness we just sleep through that
I'm not feeling good about this at all. Yesterday's "seeding " process was traumatic and barbaric done by a man without empathy. They couldn't find the clips put in at Luton so it had to be under mammography again. An hour and 45 mins later I was left traumatised in great pain and bleeding . I'm seriously wishing I hadn't had the first mammogram as this whole thing might NEVER have developed into anything. I have read medical papers questioning this very thing... overkill treatment of dcis!
Before I had the first routine mammogram, I had googled thermography and mri as alternatives as I hated the idea of radiation. Now I have had 20 mammograms ( because they couldn't position me to get the images they needed) and face radiotherapy.
I'm angry, scared and truly wish this had not been found. It is damaging my body with the stress, lack of sleep, stressful appointments and I haven't even had it done yet!!!! Also I expected several "seeds" to be put in . They only did the 2 where the metal clips had been placed. There were 5 areas though... and clips put in at the extremes... I'm really concerned that an area of dcis will be missed and I will have to go back in. I KNOW I will have to put all my trust in the surgeon but I can't help questioning this whole process.
I feel awful. Wish I was handling this better.
I've accepted nothing.
I still waiting for them to tell me they got the wrong results.
I have dics & idic invasive dics, 20;mm lump.
Had surgery to remove it , just a lumpsectomy , depends on the results as a whole what they offer.
I was offered therapy but I refused.
Now I'm waiting to see therapist.
If you can get therapy , maybe might help X
I went through this last year, and I totally share some of the other people hear who talk about feeling well and then hospital treatment making you feel rubbish. One of the things that really helped me was the Headspace app - I did 10 minutes a day from diagnosis onward there is a particularly good set of meditations about cancer specifically and I did the course twice. May not be your thing, wasn't really mine before, but I found it gave me back some faith in my own body in a weird way. Best of luck with it all.
I went through this 11 months ago and yes the positioning of the seed was horrendous but the staff were fabulous. Surgery and radio therapy were a piece of cake compared to it. I have been discharged from cancer specialist with annual follow ups. But now I am in limbo as I have tested positive for bracca2 gene and have to have double mastectomy and removal of ovaries.
I accepted having the BC and I think being positive got me through it. However my mind is in turmoil at having the other surgeries, Fear of the unknown I think as I haven’t managed to speak to anyone about either..
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2025 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007