The Long Road to a Name
There’s something uniquely painful about being told a hundred different things, only to be left holding nothing solid. H’s journey has been filled with more questions than answers and more…
Opsoclonus Myoclonus Syndrome
Our journey with Opsoclonus Myoclonus Syndrome—raw, real, and rooted in faith.
This category shares personal stories, resources, and medical insights from living through and advocating for OMS, a rare neurological disorder. From diagnosis to treatment to moments of miraculous healing, each post is written with honesty, hope, and the prayer that no parent walks this path feeling alone.
There’s something uniquely painful about being told a hundred different things, only to be left holding nothing solid. H’s journey has been filled with more questions than answers and more…
We got to the Children’s Hospital ER, and I remember the moment clearly. The calm I had been carrying started to fray. There’s a shift that happens when the staff’s…
A note from Brandi:This post includes H’s words and is shared with his permission as part of our family’s OMS journey. Some stories are best told in the words of…
There’s something about this verse that stops me in my tracks. Even when there was no reason for hope… Abraham kept hoping. Why? Because God had said. I was told…
The Second ER – Misdiagnosis #2 We made arrangements for the kids, packed bags, and headed 2.5 hours to Nashville. We arrived at Vanderbilt Children’s Hospital in the middle of…
A Sweet Night at the Ball Field On this day in 2017, Before the Shaking Began, I had been with my Lady, and I knew her family was coming into…
As I continue sharing our journey with Opsoclonus Myoclonus Syndrome, I wanted to highlight a resource that may help bring clarity to people who have never heard of this rare…
Medical information note:This post is shared for education and awareness only. It is based on our family’s experience and general information about OMS. It is not medical advice, diagnosis, or…
A Journey of Faith, Fear, and Finding God in the Chaos 8 Years Ago Our Lives Changed, our world shifted in a way we never saw coming. Our youngest son…
In the month of June, I’m leaning into something I’ve long put off and that is sharing more of our story, the unfiltered version. Eight years ago, our lives were…
A note from Brandi:This reflection is shared for encouragement, education, and personal reflection. It discusses faith, parenting, medical hardship, and trusting God in hard battles. It is not therapy, clinical…
New Video from NORD This video from NORD may be helpful for family members, friends, teachers, or anyone trying to understand what OMS can look like. Sometimes a visual explanation…
I have deep respect for nurses, nurse’s aides, child life specialists, and all the other “worker bees” in the hospital. They are fantastic and often under-appreciated. Over the past several…
Let Us Marinate on the picture. Open it up, enlarge it and just look. This canvas is a 16×20, and there is NO room left to put ANY type of…