September 29, 2025

David Baldwin

David Baldwin

Noah's Dad

We’re on day 19 of induction 1, 9 days past chemo. I’ll hit the medical highlights right off the top here:

A critical thing we’re looking for now is to see his ANC (Absolute Neutrophil Count) start to rise. Neutrophils are white blood cells that heal injuries and fight infection. The ANC has been zero for a number of days now and I am not without anxiety about that. We’re hoping to see that go up soon, but every “body” is different in that recovery.

At the same time, there are at least a few things that are better signs:

  1. Monocytes are another type of white blood cell that typically compose about 5% of white blood cells. A rise in these cells after going to zero can sometimes be a precursor to neutrophils starting to come up. Noah’s monocyte composition has risen by one percent each of the last three days from zero to three percent.

  2. Noah’s energy level is really good. He’s been doing a lot of FaceTiming, Fortniting, and Robloxing. He’s eating and drinking well and maintaining weight. It’s great to see him smiling and active and a bizarre contrast with what we know is happening in his body.

  3. Knock on wood, he’s evaded infection during this time at zero. He does receive some amount of antibiotics regularly and will continue to be closely monitored for fevers.

The hair is starting to come out quickly now and we had planned to shave his head today. He decided to keep it for just one more day as he’s doing a video call with his class tomorrow. I think he’s about ready to get rid of it because the fallen hairs on the bed, couch, shower, etc. are annoying him.

The response and support from family, friends, neighbors, classmates, etc. continues to be immense. We can’t thank you all enough for the love and caring you’ve shown us. From our families showering us with love, to friends making meals, to schoolmates making creative and uplifting cards, to people we don’t even know sending gifts and well-wishes, to our neighbors taking part in the Light The Night walk; the list goes on.

Speaking of neighbors, Steve Williams (whose daughter is in Noah’s grade) has even designed apparel and setup a fundraising webstore with all profits going to Noah at https://midwestshirtco.chipply.com/fornoah

Administrative Notes:

  • A few people had asked for more information regarding bone marrow transplant donations. NMDP was formerly known as “Be The Match” and the “National Marrow Donor Program”. I guess they’ve now gone for the abbreviation of that original name. At any rate, this is the place to go for more on joining the registry… https://www.nmdp.org/get-involved/join-the-registry

  • A “reactions” feature has been added to this site. You can now add one or more of the heart, pray, smile, and sad emoticons for any post or comment.

That’s all for now. We love you all and over and out.

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Comments (5)

Ben Wehrspann

Ben Wehrspann

Thank you for sharing Noah’s News with us. We continue to pray for him, you and your family and all of the doctors and staff taking care of Noah. I took the liberty of printing few copies of your writings for the folks at church who don’t have access to the internet. Remain positive and do not dispair! Ben
Mary Anne Harrold

Mary Anne Harrold

Thank you so much for keeping us informed. While I don't understand everything you write, I know our Lord does. And He is walking with you. Prayers to you all, especially your precious son. Love to you.
Lois Sinram

Lois Sinram

Sending much love your way and praying for you all
Sabrina Lucas

Sabrina Lucas

I love to hear the positives in the midst of all the unknown! We’ve been praying for Noah since we met you on the floor at Peyton Manning. Mayumi guided us and helped us through our first days. Praying for you all!
Amy Mier

Amy Mier

Hello, you all do not know our family at this time but I stumbled upon this page and it was meant to be . Our daughter , Hallie , who started kindergarten at Oak Trace this year also was diagnosed with Leukemia ( T-cell ALL) 1 year ago almost to this day- September 2024. I know it’s a different treatment journey that your sweet boy is on but just know I’m thinking and praying her you all. Their resiliency and strength is amazing isn’t it? May his strength continue in the fight! Please reach out if you have any questions.

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