I've been on the same treatment plan since my last post and expect to be on it a while longer. I feel good most of the time and am living my "normal" life.
I'll have a CT scan in December to check on things. My white blood count has been decreasing with each treatment (an expected side effect), and if it goes below a certain level I'll need to take a break from chemotherapy to allow it to go up.
Since I tested negative in 2012 for the BRCA1 and BRCA2 gene mutations, four additional genetic tests have been discovered that can show a higher risk of getting breast cancer. I just got my blood drawn to be tested for those and will learn in about three weeks whether I have any of those gene mutations.
If I'm negative, then my daughters will be negative for them too. That will be six genes they don't have to be concerned about.
If I'm positive for any of them, I'll learn what the implications are, and M and C could opt starting at age 18 to be tested for them. If they are positive, it will affect the decisions they make with their doctors in the future regarding what cancer screenings they receive at what ages.
I'm amazed by the advances in the cancer and genetics fields. There's such a long way to go, but there's also so much progress every year.