Imbruvica Keeps Me Alive

When the docs finally realized back in 2017 why I was sick, they concluded I had a blood disorder that at the time didn’t require any treatment. As the symptoms continued and assumedly worsened, I was put on Imbruvica, a hard to get and very expensive drug.

Every morning I take a couple of pills. They cost $300 a pill, give or take a few shekels. A bottle costs $12,000 to $14,000 a month. Not sure how I can afford it; insurance, I guess. Lucky I am in remission, though I still have to take it.

Now the US Government is investigating the Chinese company that developed it or manufactured it or distributes it. They might even have a lab next to the one that developed the covid virus. Who knows?

https://www.nytimes.com/2024/04/15/health/wuxi-us-drugs-congress.html?searchResultPosition=1

At least President Biden is aware of the problem. He wants the price reduced. I sent him a note asking him to make sure all who need it get it, along with an album of my Imbruvica images. Have not heard back from him about my note or the photos. He has other things on his plate.

 

 

Author: duckshots

Lapsed lawyer. Reader. Photographer. Jewish. Strongly attached to loving, caring, wife-Sharon. Working at remaining relevant. Hoping that my body and mind outlive my dreams. Maybe something I blog will make some sense.

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