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, 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...
Wednesday, April 6, 2016

You All Gonna Be Here When I Wake Up?

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A few days ago I said that the slow and trudging journey to a functioning immune system had finally begun with Jayne's being fully deple...
Sunday, April 3, 2016

This Place Gives Me An Uncomfortableness

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Today is the day that we were waiting for.  Jayne finished his chemo four days ago and since then it has been quite the tedious wait for his...
Saturday, March 26, 2016

No Power In The 'Verse Can Stop Me

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Most people love to share, be it their cookies, life stories, their opinion of Facebook, just about anything that can be passed on from one ...
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