Hello Everyone,
Here I am, where none of us really wanted to find ourselves, right?
After 6 months of pretty effective chemo/immunotherapy, and a week before my planned mastectomy, we learned that my TNBC had spread to my bones. At first, we felt it was curtains for me but, after an emotional roller coaster of 3 months, we have realised that - especially if you respond well to immunotherapy - you can have a pretty good quality of life, laugh, eat, travel a bit, all the time making plans, although you have more awareness of death than most people do.
I feel humbled reading what some of you have been going through.
One day it will be my turn but NOT TODAY.
