This story has been on my heart for a very long time. Seeing the recent attention given to decisions public figures have made about the lives of unborn children gave me the encouragement I needed to finally complete this project. My hope is that sharing a little of Shyanne’s story will offer parents and children helpful information in a simple, relatable way—and bring comfort to families who are facing the fears that can come with an unexpected diagnosis, something we understand all too well.
There is a quiet, beautiful truth our family has carried close for the past six years: faith can walk right beside fear, and hope can remain even when we do not know what comes next.
When our sweet daughter Shyanne was born, our world suddenly filled with unfamiliar medical words, hospital rooms, and a long list of complicated diagnoses. From the NICU to heart surgery, from hydrocephalus to a courageous battle with acute myeloid leukemia, her journey from birth to age six has included some incredibly difficult chapters.
And yet, through every hard moment, there has also been an abundance of love, a joy-filled spirit that shines brightly, and the steady reminder that Shyanne is fearfully and wonderfully made.
For years, I have wanted to help bridge the gap between sterile medical terms and the vibrant, beautiful heart of a child. I wanted to create something that could comfort parents walking a similar path, help siblings understand medical equipment without fear, and encourage children to see the person beyond a diagnosis.
Today, with a heart overflowing with gratitude, I am so thankful to finally share her story with you.
Introducing: Sweet Shyanne: The Little Girl Who Could
