I went to see my oncologist this morning. I live in a city and go to locally well known cancer clinic associated with an research hospital.
I was there for a three month check in and blood work as I have been stable on AI and Ibance for the past year. The last six weeks had been rough, due to a cold which resulted in horrible fatigue. I have really been struggling and also had some new joint pain that I posted about earlier. I know things could be worse, and I am grateful for stability.
The doctor did say that if that happens again that I could message her office and perhaps hold the Ibrance for a bit to help recover from the cold. She didn't even wait for my blood results. I probably saw her for five minutes. I think she is a good person and physician, they just don't know or care about you (every time I go in there they think that I am on Zometa, which I have declined for now). She seemed very rushed to get to her next appointment. I don't know what I expected but it is so depressing to feel unimportant. Luckily, I have a very good MD ND that I can take my complaints to re side effects. I just wish our system was better. I'm in the US and I know that we have access to things others don't. Just voicing my frustration and wishing that things could be more personal.
Letrozole weight gain
Likely secondary cancer but no information
Finished Breast Cancer Treatment
Questionable Hospital bills…
Insomnia with new brand of Tamoxifen 
