We got to see my oncologist today. She had seen in the report from my surgeon that my dad had died and was very tender and nice, offering her condolences and stuff. I was touched by her compassion and humanity.
The funniest part of the visit was getting the results of my tumour markers. When I had my Pamidronate infusion changed for the port, the nurse I talked to said that the tumour marker blood draw (which was to be done later that week) would be included in the blood done on Pamidronate day. On that day, the nurse had no orders for the tumour markers, went back to check, and came back and said that we were doing some. So they did do a tumour marker test that day; the trouble is, it was the wrong test. I was tested for CA125 (an ovarian cancer test) instead of CA15-3 (my test). At least the CA125 came back normal, meaning I have no ovarian problems. That's good, because I have no ovaries :)
So, umm, we're going to re-do the tumour marker test this next week. I hope that we end up getting the right test done this time. :) I can call and ask for the results a week after the test; if they're ok, then the nurse will call me back with them and otherwise I'll hear from my oncologist herself.
In other news, the FISH test from the last biopsy came back negative meaning that my cancer is Her2neu negative. This is actually good news, because if the FISH test showed that I was Her2 positive then the cancer would be more aggressive.
The doctor found the thickening in the latest lumpectomy scar and said she hadn't had enough experience with that scar to know whether or not that there was a real thickening. She called my surgeon and they've decided that he's going to do a follow-up biopsy. My oncologist left a message on my answering machine saying that my surgeon's office would call and set up a different kind of biopsy - I assume that this means that I'll get a core biopsy instead of the fine needle one that he did before that gave no meaningful results.
I asked her what would happen if there was a recurrence in the breast and she said that the whole treatment would change. We could do a mastectomy - some recommend it, and some don't. I think that she also implied that I'd be off of the Femara and onto something else. Hopefully we won't have to make that kind of decision.
My oncologist is scheduling a CT scan of my entire chest, abdomen, and pelvic areas as well as a bone scan. We hope to have these done before I see my oncologist again in two months. We'll also re-do my tumour markers in a month.
Oh - one final thing..... I asked about the bruising over the catheter from the port-a-cath after curling. She said that I'm not to be doing any kind of really vigorous activity because that catheter can move. So if I want to curl in bonspiels, I need to skip (call) the games - something I've tried very hard not to do. And it means that I definitely can't paddle regularly on a dragonboat team. I think I'm ok to continue bellydancing and stuff as well as most of my other activities.
Overall it was a very productive 20 minutes. I really do like my oncologist and I'm so glad that I have her as my primary oncologist.