post surgery ILC

Hi - day 6 after Surgery - I’m British and a teacher in an international school but being treated in Germany - so welcome English speaking forum - to be clear it is not the classic feel a lump - everything has been picked up on Screening - I was living in Spain until last August and had my annual screening (I’m all for this - screening starts at 45 in Spain) but my employer gave us the choice to have annual screening- to go back I had a suspect ultrasound and mammogram (called BIRADS3) so was told to go for another ultrasound 6 months later - which I did in January - and a lump around 6mm was visible which was confirmed as malignant via biopsy -  2 weeks later I have had surgery including wire guided marking for two 3mm suspect lumps - total hospital stay 4 nights - i came out of hospital on Monday (had a lumpectomy and sentinel node removal - all on public health) Now I’m  waiting for results of op - have a tumor conference next week - where all options considered and all medical team treating me present (radiologist, surgeon, consultant etc) do they happen in uk?? 

I am ER+PR+ HER2- 

Please get as many people as you can to sign the petition for screening as I am really scared that if I’d have been in the UK my cancer would not have been detected until much later.

Wondering how many of you work whilst having rads - if I could still teach for example?

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Hi

Same here.

i live in Switzerland and my two tumors were found as a result of screening.  Thank goodness for screening.

i gad lumpectomy in both breasts followed by radiotherapy.  I also work in a school but took time off to focus on myself.

i found the radiotherapy mentally quite difficult as I felt I didn’t belong in that department.  I used my free time to relax, did lots of walking and yoga.  Mind you I live in a busy household with three children and it was  during the pandemic so a little different.

good luck with everything 

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Sadly screening only picks up 85% of breast cancer.
I had a normal mammogram 6 months prior to a grade 2 triple neg tumour that I felt myself.
I think the UK screening program is ok (from 50) but definitely needs more work to encourage all women young and old to self examine.

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I am a teacher too and am off work at the moment. Can I ask how you found teaching after treatment? Do you have to take hormone tablets?