Hi @Locksley and @Blossom1961,
I don't know if dye will be used as I haven't had the first ct since treatment started at the end of October but my guess is that if will have dye based on others experience.
Not sure how often a pet scan will happen but perhaps this will happen if they suspect a progression or the oncologist might do a pet every 6 months. I just don't know yet. I am trying not to get ahead of myself worrying about what next because this whole mets thing is stressful. I am best just going day by day.
I am just on the 3rd round of Fulvestrant and Kisqali and really hopeful it works. They do have good success but I guess I have to wait and see. Sorry it didn't work for you @Julez1958. At my next round in January I will ask the oncologist for a contrast ct to see if it's working. I will also see if the ca15 markers in the blood are showing anything. I can feel some pain in my spine where the mets were found and that concerns me a little because I had radium there and had no pain for months. Then again it could be from picking my grandson up.