Thank god for the NHS routine mammograms! I've just been diagnosed with Grade 2 IDC - ER+. Stage inc HER2 to follow. Everything moving so fast and brain in whirl. Only two weeks since diagnosis, and now surgery and sentinal lymph nodes biopsy in 10 days, then prob radiotherapy and tamoxifen for 5 yrs, At the moment , drs saying no chemo will be required and v unlikely to have spread as opposite side of breast to lymph nodes as caught so early. Just can't stop my brain whirring with "what ifs", though surgeons and BCNs being incredibly supportive and reassuring.
Hi. I know exactly how you feel. I was diagnosed in November. Had lumpectomy in December and sentinel node biopsy. Luckily clear margins and clear lymph nodes. Finished radiotherapy 2 weeks ago and 5 weeks into taking tamoxifen. Its a roller coaster and i found from diagnosis to now I've not really taken it all in. Lots of sleepless nights and worrying. I'm really lucky it was caught early but the 'what ifs' are still there. Hoping to see my breast cancer nurse very soon to ask all the questions going through my mind and seeing oncologist again next month. Its worrying times and it's human nature to panic. You'll have good days and bad days but hopefully we'll all be in a position where the good days outweigh the bad. Good luck with your treatment. Let us know how you get on.
I’m in the same situation. Diagnosed on the 24th March with what I think is the same cancer as yours and now just waiting for dates…just hoping it’s soon as I want it over and done with. The odd thing is I’m not upset, not fearful only rather cross and exasperated with the damn thing. How soon after diagnosis did you get the appointment for surgery and do you have any other appointments booked prior to that?
For me it was all very quick. Mammogram, ultrasound and biopsy on 25/11, saw surgeon the week after and op on 23/12. Lots of appointments before surgery with surgeon and breast care nurse then oncologist after surgery which will be ongoing. For me it all felt very joined up, and regularly seeing medical professionals whilst on your journey. You will be taken care of and they will get you in for surgery as quickly as they can i would imagine
I'm like you - more frustrated than upset everyone is saying, "Oh you must be positive and rest and be good to yourself and are you alright?" I feel like saying, "Yeah, I'm fine, no different to the day before I was diagnosed!". My drs and nurses and the NHS trust are being brilliant. Diagnosed on 14 March, saw the consultant on 23 March and had pre-assessment the same day. Surgery is in 10 days. I asked why so quick, (glad it is though!) and they smiled and reassured me "Nothing sinister, we just like to get you dealt with asap so you can get on with your normal lives" - I hope you have same quick experience! I have to go for Covid PCR 3 days before and have the dye injection the day before. Then localisation and the surgery on the next day
So from that angle all ok - but then other times, I just think about all the " what-ifs" and other times, "Oh well, it is what it is, so just get on with it" :-)
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