Thank you, but we all go through a lot. I just wanted you to be sure that if something does not seem right, get second opinions, ask questions until you are satisfied. I learned later that there are two techniques to install a port and the one my Dr chose is the one more likely to puncture. You should not be worried about the port, as I understand this is a rare occurrence.
My tumor was 2.0cm, stage 2a, no spread. Mine probably should have simply been removed but they decided on chemo before surgery. Surgery was successful and I was declared “cancer free”, but I never feel free of it. Interesting to note that after genetic testing which my treating hospital declined to do, but Moffit recommended, I learned I had the ATM gene. I believe now that the protocol is that all TNBC patients should be tested. Good to know, as it affects the chemo choices made. I eat my antioxidants and do what I can. You might be interested in the MD Anderson study on statins and TNBC. I now take Lovastatin each day.
I am doing ok so far, but the concern never leaves me.
Very best to you.