The CT scan reveled something different. It detected the spot in the impression.
At first the doctor I felt tried to blow it off. But being the nurse and annoying patient I am, I questioned why they described it as sclerotic, a word used to describe my other mets. I sent an email to the team asking for a second radiologist to read the scans. Quickly after, I received a call from my oncologist and now on Sept 10 I get to have another bone scan, a CT scan, and an MRI of my T7. All on the same day. Pays to be persistent. If this actually comes back as another Mets, it will change my whole treatment plan. I will restart Ibrance, the $14,000/month before insurance, oral chemo and faslodex injections. Which I hear the side effects are bad. So here’s to waiting a month worrying again of what is growing in me.