Faith Journey, Medical, Opsoclonus Myoclonus Syndrome

When the Siblings Are Watching

speaking the language of rare – part 1 (4)

When your child is sick, your entire family gets pulled into the storm. What some people may forget is that there are other siblings in the home. This is about When the Siblings Are Watching – The Ripple Effect of Chronic Illness.

In our home, the impact of Opsoclonus Myoclonus Syndrome didn’t stop with one diagnosis. It hit every room, every relationship, every rhythm. And while H was the one in the hospital bed, the ones in the waiting to hear the news of his improvements or tests were his siblings—watching, holding, adapting.


The Invisible Load They Carry

They missed birthdays. There were some missed holidays.
They learned to whisper when he was home and sleeping.  My kids learned how do his exercises with him and adapt to his new way of living.

They saw fear in my eyes when I tried to be brave.
There were (still are) big emotions as they watched their baby brother shake, scream, regress—and come back again.
They learned the names of medicines most adults have never heard of.

In the end, they prayed, they played, and they waited.

And they kept loving.


How It Shaped Them

I won’t say it was easy.
It wasn’t.

But it shaped them.

They are more empathetic. More patient and more aware of invisible struggles.
They know what it means to serve without being asked, to show up without being noticed.
And I believe they are better humans because they lived through this with us.


How We Support Them

We’re not perfect, but we try.

  • Open conversations about what’s happening and why

  • Time alone with us, just them, even if it’s brief

  • Therapy, when needed

  • Acknowledgment—because their sacrifices matter

  • And lots and lots of grace


“Carry each other’s burdens, and in this way you will fulfill the law of Christ.”
— Galatians 6:2


💛 Heartbeat Moment

If you’re a parent walking this road—don’t forget the ones standing beside the bed. The siblings who are hurting and healing, too.

Let’s not just fight for the one who’s sick.
Let’s fight for the whole family.

💛 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

What You Don’t See – Life Today with OMS

What You Don’t See – Life Today with OMS

These days, life looks different than it did during the thick of H’s treatments. We’re no longer spending weeks on end in the hospital, juggling chemo, IVIG, ACTH, and emergency room visits. But just because we’re out of that season doesn’t mean the journey is over.

Life today is still challenging.
It’s just a different kind of hard.


👀 What You Don’t See

From the outside looking in, especially when he’s asleep, H looks like a typical 11-year-old boy.
He’s tall for his age. Handsome. Bright-eyed. A full head of hair. If you didn’t know him, you might never guess what he’s been through. He loves to ride his bike, play legos, listen to music, and look through books.

But then you see him around his peers—and it becomes clear that things are different.


🧠 Behind and Brilliant

H is significantly behind both academically and behaviorally. He struggles to connect with kids his age because… well, he’s never really had the chance to be “just a kid.” If you think about it, he spent a good chunk of his early life in hospitals and in isolation due to COVID-19.

He relates beautifully with younger children and older adults. It makes sense—he was raised around adults. His closest sibling in age is 8 years older and his oldest sibling is 18 years older. His world has always been full of people far ahead of him in life.

It’s no wonder he doesn’t fit into the traditional mold.


🍽️ What You Might Notice

Watch him try to eat a meal and you’ll see:

  • He might hold his fork differently.

  • Sometimes, he switches to a spoon when his tremors are worse.

  • He brings his mouth closer to his plate to avoid spills.

These aren’t bad habits. These are adaptations—skills he’s taught himself to compensate for what his body can’t always do.

He has had to relearn everything:
Sitting. Standing. Walking. Running. Jumping. Talking. Feeding himself.
Even sleeping.

That kind of restart at three years old?
That’s massive.


💪 He’s Worked So Hard

He’s had years of physical therapy, occupational therapy, and speech therapy.
And every ounce of progress has been fought for.

But even now, tremors in his hands affect his fine motor skills. Writing, buttoning, tying shoes—these are not simple tasks for him.


🏊‍♂️ And Then There’s Vitiligo

When you see H swimming, you might notice patches of skin that look lighter than others. That’s called vitiligo—a condition where the body stops producing pigment in certain areas of the skin. It’s harmless, but it makes him look a little different.

And for a kid who already feels different, every stare can feel loud.


🧨 Big Emotions, Big Triggers

H also lives with behavioral challenges linked to medical trauma, neurological inflammation, and life experiences no child should have to endure.

  • His coping skills are still developing.

  • His emotions sometimes erupt unexpectedly.

  • And between OMS moments, puberty, and trauma, things can get spicy around here.

We’re working on it. Therapy. Daily conversations. Emotional tools. So much prayer.


🤧 When Sick Isn’t Just Sick

One of the hardest ongoing realities of OMS is that when H gets sick—it’s not just a cold.

A mild virus can send him backward.
He might lose his speech for a time.
Or he loses his ability to walk.
And often, he’ll need steroids to get back to his baseline.

Once, he had the flu and couldn’t walk. Another time, a cold took his speech away.
These are not exaggerations—they are real, terrifying parts of our life.

This is why we are so careful. So protective. So hypervigilant.

We avoid crowded places during flu season.
>We sanitize. We plan.
>We protect him—not out of fear, but out of wisdom born from experience.


🙌 A Hidden Mercy

Oddly enough, H doesn’t get sick very often.

Is it the protocol we followed?
Is it because we’ve been so cautious all these years?

I don’t know.
But I do know this: I’m thankful.
Every healthy day is a mercy I don’t take for granted.


“The Lord is my strength and my shield; my heart trusts in Him, and He helps me.”
— Psalm 28:7


💛 Heartbeat Moment

He’s made it through things most adults will never face.
He’s braver than he knows, and stronger than most people realize.

So the next time you see a kid struggling to eat, or a boy who’s acting “young for his age,” or a mama who looks tired and guarded—pause.

What you’re seeing is just a glimpse.

The full story is deeper. Sacred. Hard. Holy.

H’s life may look different—but it is beautiful.
And he is doing amazing.

💛 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

Understanding Opsoclonus Myoclonus Syndrome (OMS)

Understanding Opsoclonus Myoclonus Syndrome (OMS)

Understanding Opsoclonus Myoclonus Syndrome (OMS):

What It Is and Why It Matters

As part of this series on navigating life after a rare diagnosis, I wanted to take time to share more about what Opsoclonus Myoclonus Syndrome (OMS) actually is. It’s a disorder many have never heard of, yet for the families affected by it, it becomes the center of their world overnight.

Whether you’re here because you’re walking through this with your own child, supporting someone who is, or simply trying to understand more—thank you for leaning in.

What Is OMS?

Opsoclonus Myoclonus Syndrome (OMS) is a rare neurological disorder that most often affects young children, typically between 6 months and 3 years old. It is believed to be an autoimmune condition, where the immune system mistakenly attacks healthy cells in the nervous system, particularly in the brain.

OMS is often associated with either a recent viral illness or a neuroblastoma (a type of cancer found in the nerve tissue), although in rare cases, no clear cause is ever found.

Key Symptoms of OMS:

  • Opsoclonus: Rapid, uncontrolled eye movements in all directions (sometimes described as “dancing eyes”)

  • Myoclonus: Sudden, jerky muscle movements or spasms (also referred to as “dancing feet”)

  • Ataxia: Loss of balance and coordination, which can make walking or even sitting upright difficult

  • Irritability or behavioral changes: Mood swings, aggression, and sleep disturbances

  • Speech regression or delays: Children may lose words they previously had or stop speaking altogether

Symptoms often appear very suddenly and worsen quickly, leading to a medical emergency that requires urgent attention.

Diagnosis of OMS

Because OMS is so rare—affecting roughly 1 in 5 to 10 million children—it’s often misdiagnosed or misunderstood. There’s no single test to confirm OMS. Diagnosis is typically based on a combination of:

  • Clinical presentation of symptoms

  • MRI scans to rule out other neurological conditions

  • Urine and blood tests for tumor markers (especially if a neuroblastoma is suspected)

  • Sometimes, spinal taps or EEGs

Treatment Options

There is no cure for OMS, but early and aggressive treatment can dramatically improve outcomes. Common treatments include:

  • High-dose steroids (IV or oral)

  • IVIG (Intravenous Immunoglobulin)

  • Chemotherapy agents like Rituximab or Cyclophosphamide

  • Plasmapheresis (plasma exchange)

  • Physical, occupational, and speech therapy

Treatment typically requires a team of specialists, and relapses can happen—often triggered by illness, stress, or tapering medication. Long-term care is often needed.

What OMS Is Not

OMS is not:

  • A result of poor parenting

  • A behavioral disorder

  • A temporary condition that children just “grow out of”

  • Well understood by most general practitioners

Raising awareness is key because early diagnosis and treatment can prevent long-term neurological damage.

Faith in the Unseen

For families walking this road, the diagnosis of OMS can feel like being dropped into the middle of a storm with no map. The fear, the unknown, the way life changes in a single day—it’s all overwhelming.

But even here, in this space of confusion and questions, God is not absent. He is present in the waiting rooms, in the hospital corridors, in the shaky prayers whispered late at night. He is faithful through every test result, every unanswered question, every slow and painful recovery.

OMS may have changed the story—but it doesn’t get to define the ending.

Why This Matters

There is power in sharing knowledge. There is purpose in raising awareness. And there is hope in knowing that even in the most complex, heart-wrenching diagnoses—God still writes beautiful, redemptive stories.

This post is here so others don’t feel as alone as we once did. It’s for the parent Googling symptoms at 3 a.m., the friend wanting to, the family member unsure how to help. It’s for the ones standing in the gap and believing for healing.

Thank you for being here. Thank you for caring.

Coming Up in This Series:

  • Personal reflections on how the diagnosis reshaped our daily life

  • A post (hopefully!) in my son’s own words, sharing what he remembers

  • How faith carried us—and continues to carry us—through the unknown


Have questions about OMS or want to share your own story? Feel free to reach out or comment. This is a space of grace, education, and encouragement. You are not alone.

💛 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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The Importance of Little Acts of Kindness