Well, I’m slightly more rested (only having to make bathroom trips every hour and a half), but feeling beaten down from the Neulasta. I got more hydration yesterday, but the labwork was still showing some blood coming through, so I have to go back for even more today.
At the moment, we’re not sure what’s going to be happening next to me. Well, we know that I get this hydration today and some bloodwork on Monday, but chemo-wise, things might be changing. After the way the ifosfamide (the “I” in “ICE”) treated my urinary system, Dr. C’s thinking we might need to try something else. He’s mulling over the options and will be talking to Dr. D soon to come up with the new gameplan, possibly something that doesn’t involve the ifosfamide.
I am so ready to be done with this.