Two nights ago, Caemon had the tiniest of blips on his white blood cells. Since his conditioning, his white cell count, along with his neutrophils and other forms of white blood cells, have shown up on his readouts as < 0.1, or, in other words, pretty much nothing. That’s what the conditioning chemo is meant to do. It obliterates the marrow and all these cells so that the new marrow can take over. The blip a couple of nights ago brought his white blood count (WBC) to a meager 0.2, but it was just a blip. It was an indication that things might be percolating, or perhaps that there was something there that could do some percolating. Yesterday, the count came right back down to 0.1, but it had been nice to think about.
Yesterday, the medical team came in smiling for the first time since we’ve been here, really, but not about the blip. When they entered, our boy was standing on the bed holding onto me and talking–well, protesting their entry, actually, and demanding I not talk about him–but it was talking they hadn’t heard. They were beaming, and pleased his liver numbers were decreasing, that he hadn’t had a fever in nearly a day, and that he was up and had the energy to be surly and objectionable. I was too, for as challenging as a cranky crocodile can be, it’s better than a lethargic, apathetic, constantly sleeping crocodile. A crabby croc is one with fight.
Last night, Caemon needed blood and platelets, had a bit of a fever, and was having some pain that prevented him from swallowing again. The need for blood certainly wasn’t unexpected, as he receives blood products every day, but seeing him in pain again and seeing him start to retain fluid again bothered us. His practitioners had it under control, though, so I left to get some sleep, leaving Jodi to stand watch over the boy. He had a restless night. Neither of them slept well.
Perhaps growing cells makes it harder to sleep. This morning, our son had both neutrophils and white blood cells show up on his complete blood count (CBC). His neutrophil count was 40. His WBC was 0.3. While these are still just tiny jumps, they are cells that will grow into an immune system in Caemon’s body. They are his first signs of recovery. A little more good news came in the form of lower liver numbers–the lowest they have been in some time. I cannot begin to explain the sort of hope this fosters in me.
We still have a long road ahead of us, and we can’t know until we’re on the other side of this whether we have found the darkest of the dark days or not yet, but in this moment, those sparks and flares sure do look like traces of dawn.
Yay! So wonderful to hear. Here’s to many more bleeps and hopefully some sleep for Croc and the test of the family.
Tiny steps make you appreciate your destination even more!! Way to go Caemon!
So happy to hear about his new cells. Keep growing little, croc!
Woohoo!
The dawn comes in on little croc feet. Looks like that sun is starting to break over the horizon just a bit. I can feel the light growing. Yes!
Three cheers for the surly croc! P.S. Carol, I love “the dawn comes in on little croc feet.”
Glad to hear the good news, and continuing to keep all of you, especially Carmon in healing thoughts and prayers…Praying medical staff have compassion, courage and skill/knowledge….Special prayers for Caemon’s Moms.
Blessings to Caemon and ALL that pertains to him,
Lena
Wonderful, wonderful, wonderful! It’s good to celebrate all the tiny moments of hope and victory! I’m so happy to hear C is emerging and his body is doing some truly amazing work.
Well done, Croc–Keep healing! You’re teaching us all about resilience and will, and these are lessons I keep with me everyday.
Tiniest beacons will become rays and then bursts of light! Way to go Caemon!