Thank you for this information! There was never a truer statement than what you said about being the coach, referee and the quarterback!!! Very well said! That’s exactly what it feels like while trying to figure out all the variables, doctors & treatments available to help me advocate for my healthcare. It’s exhausting, both mentally & physically. I really wish I was closer to a Mayo Clinic but unfortunately I’m in the Midwest. We do have Siteman Cancer Center locally & they have Cardio Oncologist’s on staff. My husband passed from cancer in 2015 & he received very good care at Siteman. At the time of my DCIS diagnosis I wasn’t thinking clearly or I would have gone there to begin with. Once I get the Oconotype for DCIS results & see the Cardiologist, I’m planning on going there if needed to see what’s suggested & probably continue my care. Part of my issue is that I don’t feel like I have a “team”. Currently, my Oncologist is deciding what she thinks I need. Each doctor feels like just a piece of the puzzle when not having the entire picture to work with so the pieces aren’t fitting. Thank you also for the information on Integrative Cancer Care! I’ve seen some posts about proven natural alternatives for estrogen suppression & I will definitely check into the information! I truly believe that the more educated we are, the better we can advocate for our healthcare.