top of page
  • Linkedin
  • Facebook
Search

Part Seven - Day 100 and Beyond

  • Writer: Kevin Pashuk
    Kevin Pashuk
  • Jul 25
  • 2 min read

Chapter 17

The Sentence That Let Me Breathe

April 14, 2026

Day ninety-six.

Almost there.

I was tapering steroids, which was good because they had turned me into a ravenous teenager. There were no snacks in the cupboard and no leftovers in the fridge.

I underwent another bone marrow biopsy, pulmonary testing, and chimerism bloodwork.

The gas tank remained small, but the doctors were pleased.

Then the bone marrow report arrived.

At first, I misread the title of the document as the result and felt my stomach sink.

Crap.

What does this mean?

How do I tell Leslie and the family?

Something prompted me to read the entire report again.

This time, I saw the truth:

No measurable residual disease.

That was the result we had wanted, prayed for, and inwardly hoped that it would be the finding.

The sentence represented more than relief. My body, donor cells, doctors, nurses, medications, researchers, donors, prayers, and the mercy of God had all been moving toward those words.

Statistics remained statistics.

Remission was not immortality, despite my occasional behaviour suggesting otherwise.

But the result gave me room to breathe.

It also provided a lesson that probably belongs on a mug:

Read the whole damn report before panicking.

Day One Hundred

We reached day one hundred.

One hundred days since transplant.

One hundred days of medication, monitoring, isolation, fatigue, infection precautions, complications, appointments, and waiting.

Milestones matter.

This one mattered a lot.

The cells had grafted.

The blood factory was working.

The testing showed no measurable residual disease.

Gratitude was the only reasonable response.

April 28, 2026

I was officially finished with the intensive treatment phase and moving more fully into recovery.

The doctor stopped or tapered several medications, including some that had been difficult for my organs.

It was a very good day.

Freedom after treatment did not look the way I had imagined.

I had pictured a door opening and me walking into bright sunlight with a soundtrack playing.

Instead, I received a medication taper, lingering fatigue, kidney monitoring, and instructions to remain careful.

Still, it was freedom.

The sensible-shoes version of freedom.

 
 
 

Recent Posts

See All
Prologue to this "Book"

This book began as a series of updates. At first, the updates were practical. People wanted to know what was happening, and I needed a way to tell them without repeating the same information dozens of

 
 
 
Part One - Entering the Valley

Chapter 1 The Call That Changed Everything Early on July 5, 2025, a Saturday morning, my phone rang. I did not recognize the number, so I did not answer. Persistent telemarketer, I thought. This was n

 
 
 
Chapter 2 - The Enemy Has a Name

Leukemia was now part of my vocabulary. Not exactly the word I had been hoping to add that week, but there we were. The doctors were waiting for the final biopsy details. They knew enough to begin pla

 
 
 

Comments


© 2035 by K.Griffith. Powered and secured by Wix

bottom of page