Brave Like Brynlee

Brave Like Brynlee A little girl doing big, brave things. Medulloblastoma warrior.
(2)

DX: April 2025
Here for awareness, honesty, and hope.🎗️🦄 May 2026 Little Victor 💙💛

GREAT NEWS!!!!Today is the kind of day I wish I could bottle up and hold onto forever.Brynlee’s scans are clear. No sign...
03/19/2026

GREAT NEWS!!!!

Today is the kind of day I wish I could bottle up and hold onto forever.

Brynlee’s scans are clear. No signs of reoccurrence.

And this one carried a different kind of weight, because this was her very first MRI after finishing treatment. This was the scan that quietly holds the question every cancer parent lives with in the back of their mind, the one I don’t always say out loud but feel in every part of me… did it work?

Today, I got that answer. Treatment worked.

I don’t even know how to fully explain what it feels like to hear those words after everything I’ve walked through with her. After the fear that never really lets go, the waiting, the nights that felt endless, the moments where it felt like my heart was living outside of my body just trying to keep up with it all..today, I finally got to breathe a little deeper.

And as if that wasn’t already more than enough, I was also told her MRI schedule is moving from every two months to every three. That might not sound like a big change to most people, but for me, it means more space to live in between the appointments. More time for her to just be a kid without everything constantly revolving around the next scan. More moments where cancer doesn’t get to take up quite as much room.

And then, just when I thought my heart couldn’t hold anything more..

I found out our Make-A-Wish trip is coming sooner than I expected. Disney is doing something special for Michigan Make-A-Wish families this June, and once our coordinator finalizes the dates, we will be heading to Disney World to celebrate our girl.

To celebrate her life, her strength, and everything she has fought through to still be standing right here.

From hospital rooms to castle dreams.

I keep looking at her and thinking about everything her little body has endured, everything she has overcome, and somehow she’s still the same bright, beautiful, strong little girl at her core. You did it, baby. You really did it.

I am so unbelievably proud of you, Brynlee. My warrior, my miracle, my light.

Today isn’t about fear or waiting or what comes next.

Today, we celebrate. 🩷✨


I saw a comment today that said, “hopefully you’ll move on with your life,” and I’m going to be honest..it didn’t hurt m...
03/19/2026

I saw a comment today that said, “hopefully you’ll move on with your life,” and I’m going to be honest..it didn’t hurt my feelings, it made me angry in a way I can’t even fully explain.

Because what you’re really saying when you say that isn’t kind, and it isn’t supportive. It’s that you’re uncomfortable. You’re uncomfortable with the reality that some of us don’t get to go back to who we were before cancer walked into our lives and tore everything apart. You’re uncomfortable with the fact that remission doesn’t magically restore a mother’s mind, her body, or her heart to the person she used to be.

So let me say this in a way that actually means something..

You are asking a mother to move on from the months of knowing something was wrong with her child and being dismissed over and over again. From the gut feeling that wouldn’t go away, the quiet panic that grew louder every single day, and the helplessness of watching your child change while being told everything was fine. You are asking me to move on from the moment my daughter stopped just being a little girl and became a patient, from the night my entire world shifted into something unrecognizable, from the fear that sat in my chest so heavy I could barely breathe.

You are asking me to move on from standing outside operating room doors wondering if my child was going to come back out to me. From the sound of machines, from the sterile hospital rooms, from the reality of watching my baby go through things that most adults wouldn’t survive. You are asking me to move on from the trauma of being right, from knowing deep down something was wrong and feeling what it’s like when no one listens until it’s almost too late.

That is not something a person just moves on from.

That kind of pain doesn’t disappear because time has passed or because a scan looks good. It doesn’t leave just because the word remission is written in a chart. It settles into you. It lives in your body, in your thoughts, in the way your heart drops at the smallest change, in the way sleep never really feels like rest anymore. It follows you into every good moment, because you know exactly how quickly everything can be taken away.

My daughter is alive, and I will be grateful for that for the rest of my life. But don’t mistake that gratitude for healing, because they are not the same thing. Surviving something like this doesn’t put you back together the way you were before. It changes you in ways people will never fully understand unless they’ve lived it themselves.

There is no moving on from this.

There is only learning how to carry it. Learning how to keep going while holding something this heavy every single day. Learning how to smile for your child while your mind replays the worst moments of your life in the background. Learning how to exist in a world that once almost took everything from you.

So no, I won’t move on. I will move forward, and I will do it loudly. I will tell her story even when it makes people uncomfortable. I will speak on the parts people would rather ignore, and I will never shrink what we’ve been through just to make it easier for someone else to digest.

Because this is not a chapter I can close and walk away from. This is something that lives in me, in her, in every part of our life now.

And if that’s too much for some people to hear, then maybe the problem isn’t that I haven’t moved on… maybe it’s that you’ve never had to survive something like this.


First post treatment MRI plus a lumbar puncture. Keep my girl in your prayers today. đź©·
03/18/2026

First post treatment MRI plus a lumbar puncture.

Keep my girl in your prayers today. đź©·



Tomorrow we go back.Back to the place that changed everything. Back to the halls that once held some of the worst moment...
03/17/2026

Tomorrow we go back.

Back to the place that changed everything. Back to the halls that once held some of the worst moments of my life. Back to the machines that don’t care how far she’s come, only what they might find.

It’s just an MRI to most people. A scan. A picture.

But when you’ve lived this life, it’s never just that.

It’s the memories that come rushing back without warning. The sound of doctors explaining things you never wanted to learn. The feeling of standing there while your whole world hangs in the balance of something you can’t control. The kind of fear that doesn’t go away, no matter how much time passes.

Brynlee will walk in tomorrow the same way she always does..brave, quiet, stronger than she should ever have to be at her age. She doesn’t carry the full weight of what these scans mean, and in some ways I’m thankful for that. Because as her mom, I carry it for both of us.

I carry the what ifs.
I carry the memories.
I carry the fear that sits in the back of my mind no matter how good things have been.

And I also carry the hope. The same hope I’ve held onto since the very beginning. The belief that she has already beaten so much, and that she will keep beating this too.

So tonight, I’m asking for something simple but heavy.

Pray for her.

Pray for peace over her little body as she lays there tomorrow.
Pray for strength for me, because scan days will always take something out of me.
And please, pray for clear results.

We have fought too hard to not believe in good news. đź©·


Sometimes I catch myself looking in the rearview mirror longer than I probably should.Today it wasn’t because something ...
03/16/2026

Sometimes I catch myself looking in the rearview mirror longer than I probably should.

Today it wasn’t because something was wrong. It wasn’t because I was watching monitors, waiting for a nurse, or checking to see if she was okay like I did so many times before. Today she was just sitting in the back seat, wrapped up in her pink blanket with a little bunny book in her hands, quietly flipping through the pages.

To most people, it would look like a completely ordinary moment. Just a little girl reading in the car.

But when you’re the mother of a child who has fought a brain tumor, moments like this never feel ordinary. They feel almost surreal. I look back there and I don’t just see my little girl reading a book. I see the same child who laid in a hospital bed while doctors explained scans and surgeries. The same child who has faced things most adults would struggle to carry. The same little girl who still lives with feeding tubes, medicine schedules, and the constant shadow that cancer leaves behind even after treatment.

And yet somehow, through all of it, she is still just Brynlee.

Still curious. Still gentle. Still completely captivated by something as simple as a bunny hiding under the flaps of a children’s book.

Cancer tried to interrupt her childhood in ways that will never fully make sense to me, but it never took away who she is at her core. Watching her sit back there today, quietly turning page after page, reminded me that survival isn’t always loud or dramatic. Sometimes it shows itself in the quietest moments, in the back seat of a car, where a little girl who has already fought so much is still able to find joy in a story about a bunny.

And as her mom, those quiet moments will always mean everything to me. đź©·


Tonight was one of those nights that quietly reminds me how far Brynlee has come and how many good people are still out ...
03/14/2026

Tonight was one of those nights that quietly reminds me how far Brynlee has come and how many good people are still out there in the world.

She got to go to her school’s carnival this evening, and she had such a good time. What meant the most to me, though, was the thoughtfulness behind it. Her school made sure there was time set aside for kids who need a little more space and a little less crowd, and because of that Brynlee was able to walk in and truly enjoy it. No overwhelm, no rushing through it, just a little girl getting to experience something fun like every other kid. As her mom, seeing that kind of care from a school means more than words can really explain.

Of course, one of Brynlee’s favorite parts of the night was getting her face painted. She absolutely loves it. Anything colorful, creative, and a little bit girly is right up her alley, and she sat there so excited watching it all come together. When she saw herself afterward, that smile said everything.

After the carnival, I took her out to dinner so we could end the night together. While we were sitting there, the sweetest woman came over to our table. She had asked if she could hear her story. We talked for a few minutes, and before she left she prayed for us right there. It was one of those unexpected moments that just stops you for a second and reminds you how powerful kindness and faith can be.

Tonight was filled with laughter, painted cheeks, a full little heart, and a mama who walked away feeling incredibly grateful. Grateful for a school that makes sure every child is included, grateful for the strangers who take a moment to care, and most of all grateful that Brynlee is here getting to experience nights like this. đź©·


This morning was one of those moments that quietly reminds me just how far Brynlee has come.Today she went in for her 30...
03/13/2026

This morning was one of those moments that quietly reminds me just how far Brynlee has come.

Today she went in for her 30 minute one on one homebound time at school, and I can’t even explain how much better this has been for her compared to sitting behind a computer screen. For a five year old, learning and connecting through a screen just never felt natural. Being able to walk into her school, sit with one of her teachers, and be part of a real classroom moment. Even for just a short time, means so much more to her.

Watching her participate like this fills my heart in a way that’s hard to put into words. There were so many months where normal things like school felt impossibly far away, and now seeing her slowly step back into pieces of childhood again is something I will never take for granted.

I’m incredibly grateful to Brynlee’s school and her teachers who take time out of their busy days to make sure she is included, supported, and never forgotten. That kind of care means the world to a little girl who has spent so much of her life in hospitals and appointments.

And tonight she gets another special moment, Brynlee will be able to participate in the school carnival during a small 20 minute window set aside for kids who need a little extra space and a quieter environment. It’s such a thoughtful way to make sure children like her can still enjoy the fun without the overwhelm of big crowds.

Moments like these may seem small to some people, but to us they are everything. They’re pieces of normal life slowly finding their way back to her, and I couldn’t be more proud of how brave and resilient my girl continues to be. 🩷


03/12/2026

Today Brynlee was doing her makeup, completely in her element.

If you know her, you know how girly she is. She absolutely loves it. The brushes, the colors, the little routine of sitting in front of the mirror and carefully putting everything on like she’s getting ready for something big. She studies herself so seriously while she’s doing it, and when she’s done she always smiles at herself like she knows she nailed it.

Watching her today, I just stood there for a minute taking it in.

Because the truth is, our life still isn’t what most people would call normal. Brynlee still has her feeding tube. Our days are still organized around medication schedules. And every two months we walk back into the hospital for scans that carry more weight than most people will ever understand.

Those parts of our life are still very real.

But so is this.

A little girl who has been through more than most adults could imagine, sitting happily in front of the mirror doing something she truly loves. Completely herself. Completely confident. Completely Brynlee.

To most people it might just look like a kid playing with makeup.

But to me it’s a reminder that even in the middle of everything we still carry, her spirit is untouched. She still finds joy. She still loves the little things. She still gets to be the girly girl she has always been.

My brave girl. My warrior princess. My Brynlee.

And every day she reminds me that strength can look a lot like a little girl smiling at herself in the mirror.


There is a version of me that existed before my daughter had brain cancer, and sometimes I try to remember what that wom...
03/10/2026

There is a version of me that existed before my daughter had brain cancer, and sometimes I try to remember what that woman felt like.

She slept at night. She trusted doctors when they said everything was fine. She believed that if something was truly wrong with her child, someone would catch it before it became life altering. She didn’t live in a constant state of fear, and she didn’t know what it felt like to have her entire world ripped apart in a single conversation.

I don’t live inside that version of myself anymore.

What people see now is Brynlee’s survival story. They see a little girl who fought brain cancer and lived. They see her smile, her strength, the way she’s slowly getting pieces of her childhood back. They celebrate the miracle, and believe me, I celebrate it too, because there are families who don’t get the ending we got.

But surviving cancer didn’t just leave our family with gratitude. It left me with something else that people rarely talk about.

It left me with PTSD.

Not just the kind people imagine when they think about hospital rooms and treatment, but the kind that started long before the diagnosis ever came.

The kind that comes from knowing something was wrong with your child and feeling like no one was truly hearing you.

The kind that comes from watching your child slowly change right in front of you while being told over and over again that she was fine. That nothing serious was going on. That it was probably something small, something harmless, something that would pass.

And somewhere deep inside of you, your instincts are screaming that something isn’t right.

That something is very wrong.

But the world keeps moving around you like you’re overreacting.

That kind of trauma doesn’t leave a mother’s body easily.

Then comes the day when the truth finally crashes into your life all at once, and suddenly the thing you were terrified of is real. Suddenly the words brain tumor exist in your child’s story, and everything you thought you understood about life disappears in the span of a few minutes.

People talk about the trauma of treatment, and yes, that trauma is real. But there are moments burned into my memory that I don’t think I will ever fully escape.

The trauma of watching my child physically change in front of my eyes and not knowing why.

The trauma of waiting outside operating room doors during emergency surgery, knowing that my daughter was on the other side of that wall and that there was nothing in this world I could do to protect her in that moment.

The trauma of sitting in hospital rooms trying to stay strong while your entire nervous system feels like it is collapsing under the weight of what your child is facing.

The trauma of living in a body that never truly relaxes because once you have watched your child almost die, your brain learns how fragile life actually is.

And even now, in remission, the trauma hasn’t disappeared.

If anything, some parts of it are louder.

Because now I carry the PTSD of the future.

The fear that lives in the back of my mind every time she says her head hurts.

The fear that creeps in when she seems more tired than usual.

The fear that wakes me up in the middle of the night just to make sure she is still breathing beside me, because she hasn’t slept in her own bed since the day cancer entered our lives.

She sleeps next to me now. Every night. And sometimes I lay there running my hand over her head while she sleeps, remembering the surgeries, the scans, the things that little head endured before she even had the chance to understand what was happening to her.

I am thankful beyond words that my daughter survived brain cancer.

But I would be lying if I said the experience didn’t shake me to my core in ways that changed me forever.

My body carries the physical toll of that time. The exhaustion that never quite leaves. The stress that lived in my chest for months while I watched my child fight something no child should ever have to face. The way trauma settles into your bones after you have spent so long in survival mode.

And the truth is that every parent who walks this road processes it differently.

Some parents find a way back to the person they were before.

Some parents learn how to breathe again once treatment ends.

And then there are parents like me, who are grateful every single day that our child survived, but who know deep down that a part of us will never return to the innocence we once had.

I am proud of my daughter. I am in awe of her strength. I am thankful that I still get to hold her, tuck her in, watch her grow.

But the reality of loving a child who survived brain cancer is that the world will never feel as simple or as safe as it once did.

Because once you have stood in a hospital and heard the words that your child might not make it, something inside of you changes forever.

And even though Brynlee survived that monster, the experience left scars on my heart that I will carry for the rest of my life.

That is the part of this story that people don’t always see.

Not the miracle.

But the mother who is still learning how to live in the world after it almost lost her child.


Today is International Women’s Day, and I keep thinking about the smallest woman I know..the one who changed my entire u...
03/08/2026

Today is International Women’s Day, and I keep thinking about the smallest woman I know..the one who changed my entire understanding of strength.

My daughter, Brynlee.

When people hear the word “strong,” they usually picture grown women who have lived decades of life. Women who have had time to learn, to fall down, to get back up again. But my daughter showed me that strength doesn’t come from age. It comes from the heart.

Brynlee was only a little girl when her world suddenly became hospital rooms, machines, and words no child should ever have to hear. Words like tumor. Brain surgery. Chemotherapy. Words that shake even the strongest adults.

But somehow, my daughter stood in the middle of that storm and fought.

I watched her walk into hospital rooms that terrified her. I watched tears fall down her cheeks while she still found the courage to be brave anyway. I watched a tiny girl carry a battle that most people could never imagine, and she carried it with a strength that still leaves me in awe.

People always say she’s my hero, but the truth is, Brynlee represents something so much bigger than that.

She represents the kind of strength that lives inside girls everywhere.

The kind of strength that keeps going even when your body is tired.
The kind of strength that shows up scared but refuses to quit.
The kind of strength that grows quietly inside little girls until one day the world realizes just how powerful they really are.

My daughter may be small, but her story is mighty.

She has faced things that would break most adults, and somehow she still laughs with her brothers, still finds joy in the little things, still reminds me every single day that courage isn’t loud. Sometimes it looks like a little girl simply deciding she is going to keep going.

On this International Women’s Day, I am celebrating my favorite girl.

The one who taught me what bravery actually looks like.
The one who showed me that warriors don’t have to be grown.
And the one who reminds me every day that the future is full of powerful girls who will change the world.

My daughter is one of them.



Today felt like one of those days I used to dream about when life was flipped completely upside down.Brynlee had such a ...
03/08/2026

Today felt like one of those days I used to dream about when life was flipped completely upside down.

Brynlee had such a good Saturday with her brothers. Just watching the three of them together again. Laughing, being loud, being silly the way siblings are supposed to be, filled my heart in a way that’s hard to even put into words. There was a time when days like this felt so far away, like something we might never fully get back.

Tonight we even got to go see Hoppers together, and we all had such a good time. Sitting there watching my kids laugh at the movie, whispering to each other. It might seem like something small to most people, but to me it felt like everything.

Moments like this are the ones I used to pray for in hospital rooms. The ordinary moments. The ones where my kids are just kids again.

Being able to get back to making memories with my babies like this means more to me than I could ever explain. Watching Brynlee laugh with her brothers, seeing her enjoy life again, reminds me just how much she fought for these moments.

Tonight my heart is just really full. đź©·


Yesterday was a really special little step forward for Brynlee.She went to school for her 30 minute homebound time, and ...
03/05/2026

Yesterday was a really special little step forward for Brynlee.

She went to school for her 30 minute homebound time, and while she was there she got to spend some time with her friend Delilah. Watching the two of them together again honestly melted my heart. Delilah was so incredibly sweet and gentle with Brynlee, checking on her, talking with her, just being the kind of friend every parent hopes their child has. After everything Brynlee has been through, seeing her sit with a friend, laughing and just being a kid again..it meant more than I can even explain.

So I just want to say thank you to Delilah’s parents ( Gabby ) for raising such a kind and caring little girl. Those moments of normalcy mean the world to us.

Today was another big step too. Brynlee had a dentist appointment. I knew going into it that it might be hard for her, and it was. The only thing we were able to do today was count and look at her teeth, and honestly that alone took a lot of courage from her. Going back to normal things like this can be really overwhelming after everything she’s been through medically. Places, sounds, people looking in her mouth..it all brings up big feelings for such a little girl.

But I cannot say enough good things about our dentist office. They truly put Brynlee first and followed her lead instead of pushing her to do more than she was comfortable with. They showed so much patience and understanding, and they even referred us to a pediatric dentist so she can be in an environment with extra support and care for her anxiety moving forward. That kind of compassion means everything to me as her mom.

And to top it all off, Brynlee received the sweetest card in the mail from Card Care Connection. Little surprises like that remind her just how many people are cheering her on.

Some days the victories are big.
Some days they look like sitting with a friend for a few minutes.
Or letting someone count your teeth.

But every single one of those moments takes bravery.

I could not be more proud of my girl. đź©·


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