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Cancer

Find advice & support if you or someone you know has been diagnosed with cancer

Likely breast cancer after ultrasound - thread 2

1000 replies

spartanrunnergirl · 09/04/2025 21:46

Welcome. The original thread (linked here ) was started after I had a mammogram recall and was told at the ultrasound that it was likely I had breast cancer - before biopsies were taken, and before I was ready to hear that (if you are ever ready to hear that).

I drove home gulping down tears with no idea what to do and no idea how to get through the days until my biopsy results. So I opened Mumsnet and made the original post, hoping someone might read it, and they did! One full thread later we are still sharing support, experiences, and advice. We’ve celebrated breast cancer wins and thrown virtual hugs around those who’ve needed it. (We’ve all needed it 💗)

For anyone opening this thread because they’ve found themselves in the same situation I was in … this is a hugely kind and caring bit of Mumsnet - where we’ve all felt that awful fear waiting for scans, tests, results, or with an early and uncertain diagnosis.

You are not alone.

This is the awful club - full of awesome women💗

Likely breast cancer after ultrasound | Mumsnet

Hi all after routine mammogram I was referred for an ultrasound, which I had today and the radiologist said it's likely a cancer, thus did a few...

https://www.mumsnet.com/talk/cancer/5178874-likely-breast-cancer-after-ultrasound?utm_campaign=thread&utm_medium=app_share

OP posts:
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6
BatshitCrazyWoman · 23/09/2025 19:49

I've been taking tamoxifen for 5 months, had three prescriptions in that time, and a different brand each time. I haven't noticed any difference. I'm currently taking the Tillomed brand.

@TheFormidableMrsC that sounds awful, I hope it eases soon.

KiwiFall · 23/09/2025 21:14

Triple neg breast cancer over 10 years. I was young with young children. Got cut, poisoned and zapped out! All the best to all of you currently undergoing treatment 💐

quietmaelstrom · 24/09/2025 13:40

I've been on tamoxifen since January - have had a couple of brans with no issues other than the side effects I've mentioned before.

That sounds awful @TheFormidableMrsC - hope you are back to normal soon. I've just seen that my next box is Tillomed.

Ultrasound scan this morning thankfully showed nothing of concern, so I can step back off the rollercoaster again for a while.

spartanrunnergirl · 24/09/2025 18:27

I have been on Tamoxifen for 10 months now. Not really thought about different brands but do get weird random issues so think I’m gonna track that now to see. @TheFormidableMrsCvery interesting that (and shitty for you) would be interested to know what your oncologist says. I had a random light 8 week period back in April/May after no period since starting tamoxifen and nothing since. Was referred for ultrasound of uterus and have now been referred to gynae who was unconcerned but said T causes polyps which can make womb lining thicker causing bleeding. Gynae consultant has put me on list to a have a hysteroscopy at to check me out though.

OP posts:
TheFormidableMrsC · 24/09/2025 19:01

spartanrunnergirl · 24/09/2025 18:27

I have been on Tamoxifen for 10 months now. Not really thought about different brands but do get weird random issues so think I’m gonna track that now to see. @TheFormidableMrsCvery interesting that (and shitty for you) would be interested to know what your oncologist says. I had a random light 8 week period back in April/May after no period since starting tamoxifen and nothing since. Was referred for ultrasound of uterus and have now been referred to gynae who was unconcerned but said T causes polyps which can make womb lining thicker causing bleeding. Gynae consultant has put me on list to a have a hysteroscopy at to check me out though.

That’s exactly the situation I find myself in now. Waiting for an appointment. I had what was to all intents and purposes a normal period. However it’s been five years and mine stopped with chemo. I have no idea where I am with menopause (just turned 56) because I still have a cycle every month just without the bleeding. This bleed has gone on for 3 weeks. However, it also coincided with a shocking death in my family and a new script for Tamoxifen. So who knows? BCN was unconcerned, GP was not. Hopefully we’re both ok!

BettyMagoo · 24/09/2025 22:30

Hello Ladies, thought I would just update you that I had good news today. The cancer has all been successfully removed. There was cancer in 4 lymph nodes but CT scan showed no spread so I am cancer free. So relieved. Moving forward however they want me to have chemo as a preventative measure which I wasn't anticipating followed by radiotherapy, followed by medication to put me into the menopause as you guys have been discussing. Still quite a journey ahead but feel so lucky to know that I don't now have cancer. Such a weight has lifted off my shoulders.

Vcal2017 · 24/09/2025 23:32

Hi all. I had my lump removed and 2 lymph nodes out on Monday. Today is Thursday. Feeling really exhausted and a bit depressed. I am reading a bit but I just want to sleep all the time. Is this normal?

quietmaelstrom · 25/09/2025 00:19

That is good news @BettyMagoo - sorry to hear you need chemotherapy as well as the rest of the treatment but good that the cancer itself is gone 💐

It can be normal @Vcal2017 - people's bodies react in different ways to the trauma of surgery, and your body will be have been clearing the anaesthetic drugs as well over the last few days. It's also a very emotional time apart from that. Take things gently and rest as much as you need to 🤗

Lovewine1975 · 25/09/2025 09:40

@BettyMagoo thats great news your cancer free I can imagine the feeling of relief, I get my results next week for my lumpectomy so hoping I get the same outcome. Sorry your having chemo though, must be a shock if you weren't expecting it

@Vcal2017 I had a lumpectomy three weeks ago, it took me a good 4-5 days to recover from the anaesthetic I was really tired and lethargic, just rest and take it easy your body has been through a lot

mightneedalargesnifter · 25/09/2025 12:43

@BettyMagoo Wonderful news ! Chemo will be belt and and braces approach 💐

MonOncle · 25/09/2025 20:20

That’s great news @BettyMagoo . Sorry about the chemo, I had similar in that I was told the news after my surgery. I found it hard to hear. Hope you’re doing ok!

BettyMagoo · 27/09/2025 18:37

Thank you ladies. I hope you are all doing ok. I am doing good, have an app with the oncologist this week to learn more about the plans.

@Vcal2017 as others have said. Just take things at the pace you need to. It is a big thing and as well as the physical side there is the psychological to deal with too. I am nearly 4 weeks post surgery and having felt loads better yesterday I did too much and by the end of day I was in pain and totally exhausted. Be kind to yourself and rest up. I hope you are recovering well.

cannaecookrisotto · 27/09/2025 21:14

Hello, can I join in? I never knew you guys were here!

I’m 34, diagnosed 1st September. Triple Negative, stage 3. 9cm!!! Was told it was a blocked milk duct since May but I went back to GP in August, biopsies and here I am.

I have an 8 year old and a 6 month old (hence the “blocked milk duct”.).

I’m having 12 x PC and Pembro (PC weekly, Pembro every 3), then 12 weeks of EC (every 3 weeks) followed by surgery, radio, more immuno and Christ knows what else.

Had 2 rounds of the PC so far and not had many side effects touch wood!

Nice to meet you all :)

LovingPeer · 27/09/2025 21:43

Hi @cannaecookrisotto , nice that you’ve found the group that no-one wants to be in! I’m an older patient, but it’s still a very difficult situation to be in to put it mildly. Glad you’ve got your treatment plan in place, no more waiting. Stay positive and use this group…. I have found it very supportive when you’re feeling crap!
Nice to meet you and best wishes xx

quietmaelstrom · 27/09/2025 21:55

Welcome @cannaecookrisotto

Glad you have a clear treatment plan. I didn't have chemotherapy but there are plenty here who did and will be able to help with any questions.

Hope all goes well and the side effects continue to be manageable

cannaecookrisotto · 27/09/2025 22:51

Thanks!
I can feel shrinkage already, perk of having such a large lump.

From what I’ve learnt in the past few weeks, TNBC goes chemotherapy first then surgery. Unless it’s under a certain size and I definitely didn’t qualify.

Tbh I was that elated that CT shown no further spread (except lymph nodes) after those initial weeks of waiting for the full picture that I felt like I’d won the lottery. All I could think was “how can it be this big and have stayed local in the breast”.

It’s strange how our perspective on what constitutes “good news” is now isn’t it. What I really struggled with was that initial shock. Nobody suspected BC until the biopsies came back. I had 2 ultrasounds in August, one of which by a radiologist consultant, and all come back diagnosing a “Galctocele” (huge milk cyst). Even the letter sent to my GP diagnosed this. They only did biopsies because they found it unusually large for a cyst.

Then my appointment was called forward from the 10th Sept to the 1st. Said it was a change in doctor schedules. I was expecting an appointment to discuss removal of a milk cyst, I took my mum and I’m bloody glad I did, but I think she took it even worse than me. I thought they were going to have to get the defibs out for her and I was more bothered about her. We sat down and the doctor just came out with it, I’m sorry it’s cancer, said it’s Triple Negative and the rest was a bit of a blur.

Then up until the 15th were the wave of scans. Lymph US, mammograms, MRI, CT. Then I invoked my AXA insurance and got an appointment directly with the Oncologist who would be treating me at the Christie but as a private patient. Met with Onc, she confirmed stage 3 due to size and lymph involvement and I started chemo 2 days later. I only had private healthcare because my accountant was moaning last year that I need some expenses!

The biggest thing I’ve struggled with is that feeling of having the rug pulled from underneath my life. I was plodding along in my happy little naive bubble, life was good, new baby, easy job blah blah “won’t happen to me” then in swings Breast Cancer from the left tit.

So it was like getting my head around the fact that I had Breast Cancer and that it’s an aggressive big bastard, then more so that feeling of my life snowballing beyond my control. Those first few weeks felt like I was suddenly walking a tightrope over a cavern and all the safety nets had gone. Horrible.

Now I’ve got a plan and treatment has started, it’s as though some of the nets have started coming back. It’s not spread, they’re treating to get rid, my feet are touching the floor again.

I’m cold capping but it is what it is. It the hair goes it goes. I did manage to get eyebrows micro-bladed between diagnosis and starting treatment.

Mentally, now, I’m ok. I can’t do anything except run this hamster wheel of wankery and see where it flings me off. I’m carrying on as normal as much as possible, working when I can be bothered and just doing what I need to do to keep sane in the meantime.

Sorry for the essay, it’s been cathartic!!

Vcal2017 · 28/09/2025 00:28

Hello from Australia cannaecookrisotto.
I loved your essay because it reflects so much of my experience. Less than 3 weeks ago I didn’t know I had cancer. It could be 2 weeks. Anyway, I’ve had surgery and I start radiation in 2 days. Sometimes I wish I could talk to 2 weeks ago Ruth and tell her to brighten up, she doesn’t know how easy she’s got it!
I had a partial mastectomy on Monday. At home now but with lots of dressings etc. Movement is a bit challenging. I have Stage 2 lobular cancer. Big lump too 3.2.mm. I also had an embedded Mirena removed. So it’s been a lot. I’ve stopped HRT and apparently sleeping!
I go back to work ( part time) next week. I’m curious to see what effects radiation has on me. Some people say they find not much others are wiped out. Like you I’m trying to keep things as ‘normal’ as possible but occasionally a mini freak out occurs. Wishing all the best.

SunnyValemin · 28/09/2025 09:26

@cannaecookrisotto sorry you have joined this club. I didn't have TNBC but I was diagnosed at 34 same as you. I'm about 14 months post radiotherapy now. I really get how you are feeling, it's not in anyone's plan is it. I really recommend the Younger women Together course that Breast Cancer Now run. It made me feel better being in a room of people my age. Best of luck with your chemo, let me know if you have any questions (I did 4 rounds of EC then 4 pax) xx

cannaecookrisotto · 28/09/2025 20:12

Thanks @Vcal2017 and @SunnyValemin.

I defo feel better than I did, and more so because the chemo seems to be alleviating the pain the lump was causing, so whilst I’m getting some chemo side effects (some fatigue, been lucky so far), otoh I’ve got a much smaller lump with zero pain. The first week after chemo #1, I had the worst burning pain in the lump, it was on fire! BCN said stick with it. Must have been the chemo doing its job woohoo!

Thanks for the recommendations @SunnyValemin, I’ll have a look. I’ve found some great FB groups for younger women too that have been fab!

Hope everyone is ok today ❤️

Lovewine1975 · 01/10/2025 13:37

Hiya, hope everyone is doing ok🙂
Saw the consultant today to get the results of my lumpectomy and I am officially cancer free! Which is amazing they got it all out and the lymph glands are clear, I am so relieved

However I have to have chemo and that has come as a bit of a shock, I can't stop shaking since she told me, its preventative as I had triple negative breast cancer, they want to make sure it won't come back, it will be followed by radiotherapy. I just wasn't really expecting it, maybe I should of been. Anyway looking likely to start in November, 6 cycles every 21 days I'm glad I have a bit of time to process this, and probably be back on here to ask lots of questions, such a lot to take in and think about.

Thanks xx

quietmaelstrom · 01/10/2025 16:36

So pleased for you that you are cancer-free @Lovewine1975 💐

Sorry about the chemotherapy news - a bit of a shock when you're not expecting it. Good that you have a bit of time to get your head around it. There are plenty of people here who will be able to answer questions!

mightneedalargesnifter · 01/10/2025 17:20

Delighted for you @Lovewine1975. Great news. Sorry that you have to have more treatment. Mine is the other way round. Chemo first (every 21 days - 6 rounds) to shrink first then surgery and radiotherapy, so can’t really help but they just have to throw everything at it I suppose. 💐

cannaecookrisotto · 02/10/2025 01:48

Hi @Lovewine1975

Mine is TNBC too but large so I’m chemo first. I had 3rd week of PC (paclitaxol and carboplatin) today and I’m finding it ok. First few days I feel great (think it’s the steroids) then I have a bit of a crash on days 3-4. Then seem to reset on day 5. I drink a lot of water the day before, the day of and the day after as well as an electrolyte drink. I also take a Loratadine tablet daily which has really helped with the bone pain effect from the Filgrastim. I don’t get any pain with it now. I take the anti-sickness religiously and proactively rather than wait until I feel sick. They give me Ondanestron 8mg twice a day for 2 days and metocloperamide for as required. I’ve not had to use the meto yet touch wood 🪵.

The taxol can cause some neuropathy so in the meantime, ask your unit if they provide the ice mitts/socks during treatment but if not, you can pick some up on Amazon :). My unit provide the gloves and socks but I found it intolerable, so I ordered some neoprene diving socks and gloves (Amazon again) and cut the fingertips and toes off. This way, only the bits that needed to be cold were cold and the rest were insulated. Helped lots.

I was so scared before my first treatment but it was much better than I anticipated. Keep a symptom diary so if you experience any side effects you can let your team know and they can get it sorted and tweak your meds.

TN is a bitch but it doesn’t like chemo.

You’ve got this!

Lovewine1975 · 02/10/2025 09:18

@quietmaelstrom @mightneedalargesnifter thanks I am feeling a lot more positive this morning and got over the shock of it now, realising that as much as I don't want to go through this I have to, I have a lovely family and really don't want cancer back now she's gone! Hopefully staying positive will help 😊

@cannaecookrisotto your post is great thank you, and glad your coping with it well. The chemo your on is that standard for TN do you know? thanks for the advise on the anti sickness tablets as that is one thing I am dreading, and what is neuropathy is that pain in your feet/hands? I am scared its just the unknown though, not knowing how I will react, what it will be like.

Anyone on here tried cold-capping, is it worth giving it a go?

Thanks xx

mightneedalargesnifter · 02/10/2025 09:40

@Lovewine1975 yes m doing cold cap. 5 sessions done and my hair is thinning and comes out in strands but still looks ok. They say if you can manage first 20 mins you’ll be ok and I agree. It actually doesn’t stay that cold all the way through. It does add about 2 hours onto your treatment though so be prepared for that. Give it a go!

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