I saw the oncologist yesterday - he was "running late". We waited well over an hour after a blood-letting and the usual check on vital signs by a nurse. Nothing to read other than signs on the wall about prostate cancer, lung cancer and such like.
Anyway, it seems my blood count is reasonable, low in places but no lower than expected, and not low enough to cause more time off the Ibrance or other meds. I reported to the doctor that, lately, I've been suffering arthritis-type pains in all my finger joints, and in my shoulders and elbows. I assume it is a side effect from either Ibrance or the estrogen blocker Anastrozole. He agreed, and said if it gets bad enough that I can no longer grip properly, we'll have to do something about it. Hmmm. I'd rather hoped for more, but as I can still manage to knit and type and do most things, other than opening bottles and cans, if a little more painfully than usual, I must grin (cynically) and bear it.
On the positive side, round about the same time as those new joint pains arrived, my left femur problem has seemed to lessen somewhat. I surmise that the medications have taken this amount of time to do anything noticeable enough for me to actually feel. They could have reached deep enough in my system for other, stronger side effects to emerge, along with any positive hoped for effects. Side effects so far have been some hair thinning and appetite suppression, with loss of weight (also partially caused by the lyphacitic colitis I also had diagnosed in the midst of everything else).
Anyway, my next appointment with the oncologist is at the end of February, with another CT scan to be arranged shortly before that. The doctor wants to make sure that nothing has changed in the 3 months since the last CT scan. More anxiety about results await, but I'll have a few weeks' grace before I need to worry, so I shall try to push it out of my mind.