Today I had a 30 minute infusion of Zometa. Before I began, I had some blood drawn and sent up to the lab so my creatinine could be checked. It was .8 mg/dL, which is ok for me. It’s always .7 or .8. I don’t know what it was like years ago, but it would be interesting to find out.
The nurses always tell me to drink lots of water on the infusion days. I always do! Before they start, I’ve had a liter. By the end of the day, I’ll have had at least a few more liters of water.
They had Winnie the Pooh bandaids in the chemo room today. My injection site was bleeding too much for one though, so I had it wrapped up. I got my bandaid to go.
I have to go have my INR checked now!
This is the package my thalidomide is dispensed in. The cost of the 200 mg a day as prescribed is over $1500 a month. The manufacturer has an assistance program to help folks who cannot pay, but the income requirements are so low that regular middle class people don’t qualify. If my insurance didn’t cover mine, and I had to be on 200 mg/day for a long time (like some people are), I would have to sell my house to pay for drugs! It angers me when I read about our government wasting money (or choosing to spend our money in other countries) when we have US citizens who cannot afford health care and medicines they need to stay alive.