Today
my bloods are closer to normal than they have been since this whole
thing started. They’ve been up. They’ve been down. There was nowhere
else to go. My wcc today is 17 (a little high). My HB 94 (a little
low). My platelets 271 (OK) and my neutrophils 14.8 (close enough).
On
my pathology request form today I noticed my condition as ‘CML with
blast crisis.’ That’s bad. I told them I’d feel a lot better if it just
said ‘CML’.
Today,
I said to my doctor that I’m thinking, optimistically, these first two
months of investigations and getting me stablised could be the worst
part of the whole disease. That is, if the bone marrow biopsy in a few
weeks shows no accelerated or blast cells. She said that’s possible. And
hopeful. Once I’m stable, I could tick along on my medication (the side
effects are not so bad on the lower dose, although I’m still needing a
nap every day) with a blood test every few months to just check I’m
still OK. However, if the bone marrow biopsy shows no remission, I might
be moving onto more aggressive treatment, and that means chemo and/or
a bone marrow transplant.
Here’s hoping the worst part is these few months.
Apparently, I’m looking normal. Lets hope the inside soon matches the outside.
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