I recognize most of them, and most of them recognize me. That's how it works when you become a semi-regular patient at the hospital. Even if it's on an out-patient basis. Why do I bring this up now? Because I spent most of my day in one of their semi-comfy beds yesterday.
In the morning I had a bloody nose that wouldn't stop and bleeding gums that wouldn't stop. I was a mess. Add to that some kind of funky vision problems and it was time to call the clinic. They ran some tests, did some basic stuff, then sent me off to the hospital for a unit of blood and some platelets. Dr K also added another drug to my daily regime, something that will hopefully get all this bleeding under control. Unfortunately it's 2 pills, 4 times/day. That's a lot more pills to start sending through my system. And I imagine there will be side effects to one extent or another.
The sun is shining here again today. Time to ride along with Brian to go get some fresh fish for the pond. Ours did not fare too well this past winter. A road trip may do me some good...
Have a great weekend, everybody!
skip to main |
skip to sidebar
Hats can say a lot about people
Hats can say a lot about people
About Carol
- KB (for dear Carol)
- WRITTEN BY CAROL: January, 2001: found a lump on my own. Initial diagnosis of breast cancer. Had a lumpectomy, clean margins, no lymph nodes involved. February, 2001: began 4 sessions of chemo (AC) July, 2001: underwent radiation to the right breast Sept, 2001: started Tamoxifen June, 2004: cancer metastasized to my bones July, 2004: had an oophorectomy (removal of my ovaries). Radiation to the neck. Started taking Aromasin, followed later by Femara. Began Zometa infusions August, 2005: Switched to Faslodex injections, along with the Zometa March, 2006: Still on the Zometa, started radiation to the left pelvic area. Will radiate right pelvic immediately after the left (20 sessions each) Plan is to start chemo pills, Xeloda, once radiation is complete
No comments:
Post a Comment