Hi, I’m another grade 2 diagnosed in September 2013. I found the original lump which couldn’t be seen on mammogram or ultrasound until I guided them. Lump showed up as 14mm on ultrasound and MRI scan. I opted for a double mx as it was invasive lobular cancer. After bmx the results showed 5cm multi focal - so glad I opted for bmx. Nodes came back 1/4 as microcells found in first sentinel node but no vascular. Also er+ and her2-. I’m currently waiting on oco appt on the 15th November to see what treatment I need (orgiinally told rads and tamoxifen) but after reading these posts I think chemo is now on the cards as I’m 46. So glad to read so many positive post on this forum as BC can be soul destroying if you let it.
Tracy1967 I was also told rads and tamoxifen but then was in the grey area so had to decide if I was going to have chemo. I decided to have as wanted to give myself the best chance. I started FEC x6 on 3rd Oct and have had 2 it has not been as bad as I was expecting and I chose to use cold cap which is working so far. Good luck xxx Tracy