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It feels like it’s been weeks since I last created a chart for this blog. I suppose this is because it has been weeks. Today that changes.

Over on the right is the chart that’s controlled my life for the past couple of weeks. That’s not to say there weren’t plenty of others. My potassium level seemed to be of particular concern, for example, but that would make an especially boring chart since it just bounced around between 3.3 and 3.9 the entire time. (They added a bag of IV potassium to my usual daily hydration whenever it fell below 3.6.) Now that I’m home and my IV line is gone, I’m eating more bananas than usual, just to be on the safe side, but that’s about it.

But that was nothing. What really mattered was my white blood count. You can see it on the right. For some reason, the two days of actual chemotherapy are called Day -2 and Day -1, and the day of the stem cell transplant is Day 0. On that day, as you can see, my count was around 6500, which is quite normal. Then, as the Melphalan steamrolled everything in its path, it plummeted to ~0 on days 7 and 8. Bye bye, immune system. Finally, on Day 9, as the transplanted stem cells started to morph into various blood products, my count skyrocketed. By the time I was discharged on Day 14, it was back to normal levels.

Fascinating, no? Especially when it’s in chart form!

Lessee. Any other news? My fatigue is still pretty heavy, and will stay that way for 2-3 weeks. I didn’t realize it would last so long, partly because my doctor waited literally until my discharge date to tell me. But it’s for real. It took me two tries to create this post: one session to create the chart, after which I crashed, and a second session to write the text. Not exactly speed demon blogging. What else? I have a nasty metallic taste in my mouth all the time. It sucks. And I think my hair is finally getting ready to fall out completely. This morning my pillow was covered with tiny little pieces of hair, and it’s pretty obvious where they came from. On the bright side, my appetite is improving. I’m not yet at the stage where I really want to eat, but I’m mostly willing to eat, which is good enough for now. This may be partly due to the fact that I’m wearing one of those seasickness patches behind my ear to fight nausea. It seems to be working.

Oh, and I can now take a nice, normal shower without first having to spend ten minutes trying to bundle up my catheter so it doesn’t get wet. Woohoo!

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