The Boy They Call Jayne

Jayne Wood is my four month old son who was diagnosed with AML, a type of leukemia. Because this type of leukemia, and the subsequent chemotherapy, depletes his immune system to almost nothing, this blog will document, capture, and extol the journey of Jayne, his parents, the medical staff, and his family while battling cancer before he could even walk. "Jayne stood up to cancer and gave it what for, our love for him now ain't hard to explain, the hero battlin' cancer, the boy they call Jayne."

Wednesday, June 8, 2016

Made By A Person Who Longed To See A Swan

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This week has been a week of lasts.  Sometime this evening will be Jayne's last chemo injection.  It is both an immense relief and a sub...
Saturday, June 4, 2016

And If We're Very Very Lucky, They'll Do It In That Order

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The home stretch lies before us.  Within a month or so, the hardest part will be past.  His MRDs have all come back at 0%, there doesn...
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Wednesday, May 11, 2016

But These Apples Are Healthsome Good

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It has been two weeks since we began his third course of chemotherapy and we're still waiting for his ANC to drop to zero.  Part of the ...
Wednesday, May 4, 2016

Whose Color Is He Flying?

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Little more than two days out from his last chemo injection and Jayne is having the worst time so far.  Since day five or so of his injectio...
Monday, May 2, 2016

Well My Days Of Not Taking You Seriously Are Certainly Coming To A Middle

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Well, it's certainly been a while but today, at around 2 in the morning, was Jayne's last chemo treatment for his third round of che...
Sunday, April 17, 2016

Planet's Coming Up A Mite Fast

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The past few days have been quite eventful indeed.  Not only has wee baby Jayne been crawling around the entire hospital room roaring like a...
Thursday, April 7, 2016

He Was Non-Specific As To How

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So, while not everything has righted itself with Jayne's inevitable recovery, there is a bit of light amidst the hazy gray of a hospital...
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