Thought I'd better write about today's hospital visit, before I forget what's what..
Saw Dr P, who informed my that my bilirubin levels are almost back to normal now. Normal is 4-22. Mine's 24. Which, considering it was 250, at in January, is good!
We don;t know if it's because of the stent, or if the chemo's shrunk the tumours, so reduced the obstruction in my bile ducts. I suppose it's likely to be a combination of both.
While my bilirubin's gone down, other liver function results have gone up a bit, which could be cause for concern.
It could mean the capecitabine's not working as well anymore. Or it could be something else that's affecting it.
It's not great that they've gone up anyway. Liver scan's been ordered.
Over the past month or so, I've been having pain in my shoulder too. We know there are bone mets there, so it's likely that they're worsening too.
I'll be having a few blasts of radiation on my shoulder, to hopefully help with the pain.
Dr P's also referring me back to Nottingham City Hospital, now we know the Lapatinib/Tykerb trial's still open (for now). I just hope I'm still eligible for it, and I manage to get there before the trial closes.
While I was there, I got my prescription for cycle 6 of capeciatbine/Xeloda.
Not much else to report today.. I'm tired from hanging around the hospital all day.
Dr P was running behind, which I never mind, because I know he doesn't rush his patients. He always has plenty of time for us.
Then I had my zometa infusion. They found veins to take blood, and for the zometa, first time, which is quite unusual for me!
Showing posts with label bone cancer. Show all posts
Showing posts with label bone cancer. Show all posts
Tuesday, 29 April 2008
Tuesday, 25 September 2007
Cancer's Back Again
Today brought my oncology appointment. Which brought MRI scan results. Which brought the news that I'd feared. The cancer's now in my bones too.. in my shoulder, and in my pelvis.
I don't know what the treatment plan is yet. It could be another six weeks before I find out. That will be over three months from having the bone scan.
They have to decide whether to do nothing. Whether to give me more chemo. Whether to give me bone strengthening drugs. Whether to give me radiotherapy to help with the pain. Or whether to give me a combination of the above.
Meanwhile, I'm left hanging, and wondering what wonderful voyage around my body, the cancer's taking while I'm waiting.
Not the happiest of bunnys, tonight.
Labels:
bone cancer,
bones,
breast cancer,
cancer,
chemo,
oncology,
pain
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