Faith Journey, Medical, Opsoclonus Myoclonus Syndrome

Trudging Through the Muck of Life

Trudging Through the Muck of Life

Let’s be real…parenting is hard. Here I am, Trudging Through the Muck of Life.

Parenting a child with a rare disorder like Opsoclonus Myoclonus Syndrome (OMS)? That’s a whole different level of hard. Some cases of OMS are tied to a type of childhood cancer called neuroblastoma. Others, like ours, are idiopathic—which is a fancy way of saying, “We don’t know why this happened.”

One day, our son was a typically developing, healthy child.
The next day, it was as if someone hit the reset button on his entire body.

He could no longer walk, sit, speak clearly, or feed himself. His hands and legs shook uncontrollably, much like the tremors seen in Parkinson’s disease. It was like having a newborn in a toddler’s body—except with rage, fear, and confusion layered on top.


Support, and Still Alone

We are incredibly grateful to have a loving support system. Family, friends, our church, and his team of therapists and doctors have come alongside us. There have been meals, prayers, encouragement, and plenty of tissues passed our way.

But only those of us who live in the trenches with him—every single day—really see it. The raw. The relentless. The moments we never expected to still be living.

What people don’t realize is that medical trauma leaves a mark.
Even as we’ve moved past the life-or-death stage and into what some might call “maintenance,” the emotional and behavioral toll lingers.

And that’s what we’re trudging through now.


When the Outside Doesn’t Match the Inside

Our son looks like a typical 11-year-old. But developmentally? He’s closer to 6. And when a child “looks” typical, people expect them to act typical.

They don’t see the hard wiring that’s been altered by trauma, medications, and daily battles just to stay regulated. They don’t understand that what seems like defiance or stubbornness may actually be overstimulation or fear. That his arguing isn’t about winning—it’s his way of grasping for control in a world that feels chaotic inside.

He can be fiery, impulsive, and loud.
Also, he struggles with sitting still, following instructions, managing big feelings.
He also has a heart the size of Texas, a smile that lights up rooms, and a brain that’s constantly working harder than most people will ever know.


Mourning and Readjusting

There are moments when I forget.
When I think, “We’re caught up. We’re good.”
Until he’s with peers… and the difference is painfully obvious.

And I mourn.
I mourn the “normal” I once knew and have to readjust to the beautiful, challenging, very real version of normal that we live now.

We keep trying new things. Gluten-free diets. Weekly therapy. Natural calming supplements. Educational supports. Consistency. Grace. Repetition. So much repetition.

And still—some weeks are just plain exhausting.


Naming Emotions, Naming Grace

One of the ways we’re helping him process the trauma and learn emotional regulation is through emotion cards. We’ve taped them to the fridge, his bedroom wall, and even put them in his backpack. We role-play, talk through scenarios, and practice statements like:

“I feel sad because kids at school won’t play with me.”
“I feel angry because I don’t like to be told no.”

Sometimes, we sit on the floor for nearly an hour, just naming what hurts.
Sometimes, when he’s done, he simply says, “Let’s move on.”
And we do.


What I Need You to Know

I’m tired. I’m honest enough to say that.
But I’m not giving up. Not even close.

I would choose this child—this life—a million times over, even on the hardest days.
He is mine. He is meant for me. And I will keep fighting for understanding, connection, and healing every day we’re given.

But I also need you to know this:

If you see a mama struggling with a child who “looks fine” but is melting down,
please don’t judge. Don’t offer unsolicited advice. Don’t scowl or whisper.

Offer a smile. A silent prayer. A moment of grace.

Because what you see is a fraction of what life looks like for families like ours.
Most diseases are invisible. Most battles are internal. And most of us are doing the best we can with what we have.


“The Lord gives strength to His people; the Lord blesses His people with peace.”
— Psalm 29:11


💛 Heartbeat Moment

Grace doesn’t cost you anything to give—but for someone else, it may be the only thing keeping them going.

Love more. Judge less.

And if all else fails… just be kind.

💛 If you’re navigating life’s hard places and need a safe space to heal, grow, or just breathe—Circle of Hope Counseling Services is here for you.

We offer trauma-informed, faith-filled therapy for individuals, couples, and families.

📞 Reach out today to schedule your first session (KY residents only) or learn more: Circle of Hope Counseling Services.

You don’t have to walk this journey alone. Hope starts here.

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Faith Journey, Medical, Opsoclonus Myoclonus Syndrome

Praising God in the Cold and the Storm

before the shaking began (8)

There’s this image I used to carry—me, my family, sitting around a cozy campfire, singing Kumbaya. Everything is warm, glowing, peaceful. That’s how life feels when everything’s running smoothly. When you’ve got that rhythm. That flow. Here I am, Praising God in the Cold and the Storm.

But what happens when the fire starts to die?


When the Fire Goes Out

You feel it—things shifting. The air gets colder. Your fire starts to fizzle. You frantically grab whatever you can find—scraps of paper, bits of old wood, anything to keep it alive.

Then, out of nowhere, a bird flies overhead and pees on your ember.
Gone. Just like that.

No flame, no light, and no heat.
You sit there… cold.
You think it can’t get worse.
But it can.

You realize you’ve eaten your last s’more.
>No heat. No light. No food.
It’s doable. It sucks. But it’s doable.

And then?

The monsoon hits.

Suddenly, you’re drowning in it. The weight. The grief. The fight. The diagnosis. The not-knowing. The knowing-too-much. The never-ending appointments. The medicine. The meltdowns. The rage. The silence. The fire feels like it will never come back.


This Past Year

That’s what this last year has felt like.

Once we received the official clinical diagnosis, everything changed.
And yet… nothing was fully certain.

There is no single test for Opsoclonus Myoclonus Syndrome (OMS). It’s not black and white. No MRI, LP, blood panel, EEG, or X-ray can definitively say: “This is what your child has.” It’s a combination of symptoms, observations, and the experience of doctors willing to say what others can’t.

It’s living in limbo with a name that doesn’t always behave like it’s supposed to.


Protocol After Protocol

We started the “standard” protocol.

  • High-dose steroids while hospitalized

  • Monthly IVIG

  • Four rounds of Rituximab (a type of chemo)

  • When that didn’t help, we added ACTH (daily high-dose steroid shots)

ACTH brought an unholy level of rage, insomnia, and OCD.
I watched my sweet boy disappear into something wild and constantly panicked.

He lived in fight or flight.
And so did I.


Second Opinions & the Blessing of Brutal Honesty

I got a second opinion—without permission. Because when you’re a mama in the storm, you do what you must.

This doctor was honest. Blunt. And honestly, I needed it.

She didn’t immediately see signs of OMS and she believed the progression was more aggressive. In the end, she suggested starting over—repeating all the tests.

We did.

And wouldn’t you know? While in the hospital, his ocular flutter returned.

She circled back and agreed: it most likely is OMS.

“Blessed is the one who perseveres under trial because, having stood the test, that person will receive the crown of life…”
— James 1:12


Zebra vs. Okapi

In the medical world, doctors are taught:
“When you hear hoofbeats, think horses—not zebras.”

A zebra means something rare. Something unlikely.
We were sure H was a zebra.

But we were wrong.

He’s not a zebra.
He’s an okapi.

Strange. Rare. Beautiful. Mysterious. And completely misunderstood.

And in some holy, divine humor—the okapi just so happens to be my all-time favorite animal.

Go figure.


💛 Heartbeat Moment

Praising God in the storm doesn’t always look like singing around a fire.
Sometimes it looks like sitting in the cold, soaked to the bone, whispering,
“God, I trust You,” even when your teeth are chattering and your heart is tired.

Sometimes praise is a whisper.
And sometimes it’s tears.
Sometimes it’s survival.

But it’s still praise.

Because even in the rain… even in the dark… even when the fire is out…

God is still God.

And the fire? It always comes back.

“When you pass through the waters, I will be with you…”
— Isaiah 43:2

💛 If you’re navigating life’s hard places and need a safe space to heal, grow, or just breathe—Circle of Hope Counseling Services is here for you.

We offer trauma-informed, faith-filled therapy for individuals, couples, and families.

📞 Reach out today to schedule your first session (KY residents only) or learn more: Circle of Hope Counseling Services.

You don’t have to walk this journey alone. Hope starts here.

 

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