Hi there TNBC sisters. I was diagnosed 6/2015 and am now approaching my 8 year anniversary (end of treatment). I had stage 2b with no nodes involvement. 12 taxol, 4 AC, lumpectomy, 36 rads and then xeloda (I had to fight for that). I followed with Zometa (I also had to pursue on my own).
At the time I completed treatment I was told they would not be scanning me or running blood tests to keep an eye on things. There is a part of me that is okay with that and a part of me that is not. I would love to know what all of you have been doing and what you were told the procedure would be for when you were all done. I was treated at UCSD in San Diego and to be honest, my Dr made me feel like it was a hopeless cause and that I was going to die anyway. Ended up with PTSD from her.