Brave Like Brynlee

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

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

We’ve had a good, quiet week over here, and if you know anything about this life, you know quiet is exactly what we dese...
08/22/2026

We’ve had a good, quiet week over here, and if you know anything about this life, you know quiet is exactly what we deserve. No big appointments. No scary news. No rushing from one thing to the next. Just a little space to breathe, enjoy each other, and let life feel normal for a minute.

And speaking of normal, Brynlee found out who she’ll have for kindergarten, and she could not be more excited. She is so ready to start school with everybody, see her friends, learn new things, and just be a kid again. There is something about watching her get excited over something as simple as going to school that gets me every single time. After everything she has been through, these ordinary childhood moments feel anything but ordinary to me.

Next week gets busy again. She finishes speech therapy at Briarwood and will continue receiving speech at school. She also starts PT again on Monday, and once school begins she’ll be receiving both PT and OT there as well. She has her open house next week too, so she’s already excited to walk back into school and see some familiar faces again.

And through all of it, she is just doing amazing. Truly. She keeps growing, learning, getting stronger, and showing me more and more of herself every day. I am so incredibly proud of her and how far she has come.

Tonight we went out to dinner together and just had a good time. Nothing huge, nothing fancy, just one of those simple nights where I got to sit with my girl, watch her smile, listen to her talk, and soak it all in.

After a life that has felt anything but simple, I think I’ll always have a special kind of gratitude for weeks like this. Quiet. Happy. Normal.

Exactly what my girl deserves. đź©·


Today felt like summer is supposed to feel. Brynlee spent the day outside, running around, eating pizza, laughing, and e...
08/16/2026

Today felt like summer is supposed to feel.

Brynlee spent the day outside, running around, eating pizza, laughing, and enjoying these last few weeks before summer starts slipping away. Nothing fancy, nothing planned, just one of those simple days that somehow ends up meaning so much more than you expect it to.

I found myself watching her a little closer when she was trying to run. She’s definitely not all the way there yet, and sometimes it’s more of a really fast walk than an actual run, but the difference I’m seeing in her confidence is huge. She’s trusting her legs more. She’s moving faster without hesitating as much. She’s starting to believe in her body again, and that alone makes me so incredibly proud.

There was a time when so much of her independence was taken away from her. Her strength, her balance, her confidence in her own body. So seeing her outside now, trying to keep up, pushing herself a little more, and just enjoying being a kid feels bigger than I know how to explain.

I’m so proud of how far my girl has come. Not because she has to prove anything, and not because recovery has to happen on anyone else’s timeline, but because I know how hard she has worked for every little piece of herself she has gotten back.


Sometimes I look around at all the love that has found its way to Brynlee, and it gets me right in the heart.The cards i...
08/15/2026

Sometimes I look around at all the love that has found its way to Brynlee, and it gets me right in the heart.

The cards in the mail. The little packages. The toys picked out just for her. The sweet messages tucked inside from people who simply wanted to make her smile. Some of you know her personally, some of you have followed her story from miles away, and some of you have never even met my girl, but you still took the time to remind her that she is loved.

Thank you. Truly.

After everything Brynlee has had to see and experience at such a young age, one of the things I want most for her is to still believe there is so much good in this world. I never want cancer, hospitals, fear, or all of the hard things she has been through to become the loudest part of her childhood. I want her to remember the kindness too. I want her to remember that people showed up. That strangers became friends. That an entire community wrapped their arms around her and celebrated every little piece of her being here.

Every card she opens and every surprise that makes her face light up is another little reminder of that.

So thank you for loving my girl. Thank you for thinking about her. Thank you for giving her reasons to smile and for showing her, over and over again, that even after some of the darkest days, there is still so much good waiting on the other side.

I don’t think I will ever be able to fully explain what it means to a mom to watch people love her child so well. But I hope you know I notice it. I remember it. And I will always be grateful for every single person who has helped make Brynlee’s world a little brighter. 🩷


Today was a speech therapy day, and somehow these appointments have a way of making me feel proud and heartbroken at the...
08/12/2026

Today was a speech therapy day, and somehow these appointments have a way of making me feel proud and heartbroken at the exact same time.

Brynlee is doing so good. Right now, one of the biggest things we’re working on is emotions. Not just recognizing them, but learning how to explain what she is feeling without becoming so overwhelmed that she shuts down and doesn’t want to talk about it anymore. That sounds like such a simple thing until you’re sitting beside your child watching her try so hard to find the words for something happening inside of her.

There are moments when I can see the frustration all over her face. She’ll be trying to remember something or understand what she’s being asked, and when it doesn’t come to her right away, she gets so upset with herself. That part hurts my heart more than I know how to explain. I wish I could reach into her little brain and make everything easier for her. I wish I could take away that frustration and remind her that she isn’t doing anything wrong just because something takes her a little longer to grasp.

But then she gets it.

Today she was so proud to show me how she was matching all of the animals together in the picture, pointing everything out like, “Look, Mom!” And of course I looked. I will always look. Because after everything she has been through, I don’t think I’ll ever take those little proud moments for granted again. Watching her learn, remember, communicate, and keep trying even when something is difficult feels enormous to me.

And apparently she wasn’t finished making me proud today.

Last night, Brynlee slept in her own bed ALL NIGHT. And the best part is that she decided to do it completely on her own. Nobody pushed her. Nobody made it a big thing. She just decided she was ready.

I know sleeping in your own bed might sound like the most normal childhood thing in the world, but normal things hit differently around here now. Every little piece of independence she takes back feels like another tiny piece of childhood finding its way back to her.

So today I’m proud of the little girl who is learning how to put her feelings into words. I’m proud of the little girl who keeps trying when remembering something feels harder than it should. I’m proud of the little girl who proudly shows me every animal she matched correctly. And I’m really, really proud of the little girl who crawled into her own bed last night and decided all by herself that she could do it.

Hopefully this is the beginning of many more nights in her own bed. 🤞🏻 But even if it takes time, she’ll get there the same way she has gotten through everything else.

One brave little step at a time. đź©·


Today was Brynlee’s six month checkup with neurology, and thankfully, she is doing really good. Her doctor is happy with...
08/11/2026

Today was Brynlee’s six month checkup with neurology, and thankfully, she is doing really good. Her doctor is happy with how she’s doing, and that is something I will never take for granted.

But today still felt weird.

Somehow, an entire year has gone by and today I found out for the first time that my baby has a metal plate in the back of her head.

A whole metal plate.

I know that probably sounds like just another medical detail after everything she went through, but hearing it caught me completely off guard. I sat there thinking about how much happened to her little body in such a short amount of time, and how there are still pieces of it that I’m learning even now.

We also talked about the skin around her scar. It is still very thin because of the chemotherapy and radiation, but over time it should begin to thicken again. Another small reminder of what treatment took from her body, even while it was saving her life.

That is the strange part of all of this.

Brynlee is doing good. She is happy. She is moving forward. She is growing, learning, laughing, and becoming more herself every single day.

And yet appointments like today have a way of pulling me right back into everything she had to survive to get here.

Sometimes I look at her and she just looks like my happy little girl again. Then someone mentions radiation damage, scar tissue, a metal plate in her head, or something else left behind from treatment, and suddenly I remember just how much her tiny body has been through.

I think that is why my emotions feel so all over the place today.

I am so incredibly grateful for where she is now. I know how lucky I am to hear that she is doing well.

But I also think there will always be a part of me that aches when I’m reminded of everything it took to get her here.

A year later, I’m still learning pieces of her story.

And somehow, I’m still trying to process it too.


Lately, I’ve been trying to figure out when I became so angry.Not just angry about one thing. Angry in this deep, exhaus...
08/11/2026

Lately, I’ve been trying to figure out when I became so angry.

Not just angry about one thing. Angry in this deep, exhausted way that seems to sit right under my skin all the time. I can have a perfectly normal day and still feel it there. I can be making dinner, folding clothes, driving somewhere, listening to Brynlee laugh from the other room, and suddenly I can feel this ache in my chest that I don’t even know what to do with.

I think a lot of it is resentment.

And that is such an ugly word to admit when you are also so unbelievably grateful.

I am grateful that Brynlee is here. I am grateful that she is in remission. I am grateful for every ordinary thing I used to take for granted. Watching her play. Hearing her talk. Seeing her excited for school. Listening to her laugh. Watching her be a little girl again.

But somewhere along the way I realized that gratitude did not erase what happened to us.

It did not give me back the mother I was before cancer.

Before all of this, I worried about my kids the way mothers do. I thought about accidents. I worried when they were sick. I wondered if they were happy or if I was doing enough. But there was still this quiet belief underneath all of it that our lives were basically safe. That really terrible things happened somewhere else. That if something was wrong, a doctor would figure it out, we would fix it, and life would keep going.

Then cancer walked into my house through my daughter.

And once you have watched the worst thing you can imagine happen to your own child, you cannot make your brain forget that it is possible.

That is the part I struggle to explain.

I can look at Brynlee now and see a happy little girl, but I can also remember what it felt like to be terrified of losing her. I can hear her complain about something completely innocent and feel my stomach drop before I even have time to think. I can tell myself a hundred times that she is okay and still have that little voice in the back of my head asking, “But what if she isn’t?”

I hate that voice.

I hate that I know exactly how quickly normal can disappear.

I hate that there was a time I did not know what medulloblastoma was, and now I could probably explain more about childhood brain cancer than I ever wanted to know in my entire life.

I hate that I can never go back to being the mother who hears a headache and just thinks, headache.

There is always another thought behind it now.

And it is exhausting.

It is exhausting to love someone this much and also know, in the most real way possible, how badly the world can hurt them.

I think that is where so much of my resentment lives.

It lives in the life I had before I knew any of this.

It lives in the fact that my daughter had to lose pieces of her childhood to hospitals, treatments, scans and fear.

It lives in every part of me that still feels like I am waiting for the other shoe to drop even on the happiest days.

It lives in the fact that life did not stop needing things from me just because I was traumatized.

There were still children who needed me. Still meals. Still schedules. Still school. Still appointments. Still laundry. Still decisions. Still a million tiny things that somehow needed to get done even when I felt like I could barely hold myself together.

And sometimes I get so tired of being the person who has to keep everything moving.

That is probably the hardest thing for me to admit.

There are days when I feel like I am carrying the emotional weight of what happened to Brynlee while also carrying all the regular weight of motherhood, and I am just tired.

Tired of remembering everything.

Tired of worrying about everything.

Tired of thinking ten steps ahead.

Tired of being scared.

Tired of trying to look normal when my mind still doesn’t always feel normal.

And then the guilt comes, because how dare I feel anything except grateful when my daughter survived?

But I have slowly realized that those things are not opposites.

I can be grateful that she survived and furious that she ever had to.

I can be thankful for remission and still hate the fear that came with it.

I can love this life because my children are in it and still hate what parts of this life have done to me.

I can look at Brynlee and feel so much love that it hurts, while also grieving the version of motherhood I lost when cancer taught me that loving your child with everything you have does not make them untouchable.

That knowledge changes you.

It changes the way you sleep.

It changes the way you hear certain words.

It changes the way you sit in waiting rooms.

It changes the way you look at a normal fever, a headache, a tired afternoon.

It changes the way you imagine the future.

And some days I resent that more than I know how to say.

I resent that fear follows joy now.

I resent that even the happiest moments can come with this quiet plea in my head.

Please let me keep her.

Please let this stay good.

Please let us have more time.

I hate that those thoughts exist at all.

I hate that childhood cancer has made me angry at a world that somehow keeps moving while children are still being diagnosed, still being treated, still dying, and families are still being forced to live through the exact nightmare I would not wish on anyone.

I hate how little people realize what childhood cancer leaves behind.

Because remission is beautiful, but remission is not a magic eraser.

It does not erase what your child went through.

It does not erase what you saw.

It does not erase the fear.

It does not erase the anger.

Sometimes it just means the crisis becomes quieter.

And now you are left trying to figure out how to live with everything that remains.

I wish I could say I have figured that part out.

I haven’t.

Some days I am hopeful. Some days I am grateful beyond words. Some days I feel almost like myself again.

And some days I am angry that this is my life.

I am angry that cancer touched my baby.

I am angry that it changed me.

I am angry that I am scared of things I never used to think twice about.

I am angry that I can never unknow what I know now.

And underneath every ounce of that anger is the same thing.

Love.

The kind of love that makes fear unbearable because there is nothing in this world I want more than to watch my children grow up.

So I keep going.

Not because I have made peace with any of this.

Not because I am always strong.

Not because remission somehow fixed me.

I keep going because Brynlee is here.

And I will spend the rest of my life being grateful for that.

Even on the days when I am still furious about everything it took to get here.


This week, I caught myself smiling more than I have in a while.Not because anything huge happened. There wasn’t some big...
08/07/2026

This week, I caught myself smiling more than I have in a while.

Not because anything huge happened. There wasn’t some big milestone or life changing appointment. It was just one of those weeks where I got to watch Brynlee be exactly who she’s meant to be.

Every morning she has been excited to get up and go to summer school. She talks about her day before we’ve even made it home, bouncing from one story to the next, making sure I know every little detail that made her smile. I love listening to her because she tells stories with her whole heart. Half the time she’s so excited she can barely get the words out fast enough.

She’s doing so well with her speech, and this week she got to work with OT too. It’s so easy to look at those things as therapy sessions, but to me they’re little pieces of her confidence growing. Every week I see a little more independence, a little more determination, and a little more of the little girl she’s always been shining through.

The biggest difference lately, though, has been her energy.

She doesn’t slow down.

She’s talking, laughing, dancing through the house, making up games, asking a million questions, and somehow still finding enough energy to keep all of us on our toes. I swear our house feels brighter when she’s in one of her happy moods.

I think as parents we spend so much time waiting for the next appointment, the next scan, the next therapy, the next thing..that we forget to stop and notice the beautiful weeks in between.

This was one of those weeks.

A week filled with learning, laughter, happy little stories after school, and a little girl who reminded me that joy doesn’t always come from the biggest moments. Sometimes it shows up in backpacks by the front door, excited chatter all the way home, and hearing, “Mom! Guess what happened today!”

Those are the moments I’ll hold onto forever. And I couldn’t be more proud of my girl. 🩷


I’ve realized that I haven’t really been thinking about kindergarten.I’ve been thinking about preschool.The last time I ...
08/04/2026

I’ve realized that I haven’t really been thinking about kindergarten.

I’ve been thinking about preschool.

The last time I watched Brynlee walk into a classroom, she was just a little girl. She had no backpack full of hospital memories. No scars. No therapies. No word called remission attached to her name. She was just my baby, running into class without either of us knowing that a brain tumor was already quietly changing the course of our lives.

If someone had stopped me that morning and told me it would be the last time I’d watch her walk into a classroom before cancer took over our world, I never would’ve believed them.

Not long after, everything changed.

Instead of getting ready for Young 5’s with the other kids, our days became filled with MRIs, surgeries, chemotherapy, radiation, therapies, homebound lessons, and learning how to survive a life I never imagined we’d have to live. Childhood kept moving forward around us while ours stood completely still.

And now, after all of that..

My little girl is getting ready for kindergarten.

People see a first day of school.

I see answered prayers.

I see every doctor, every nurse, every therapist, every teacher who helped carry her to this moment. I see every night I sat beside her bed wondering what tomorrow would bring. I see every scan that stole my breath before I heard the words I was praying for. I see every impossible day that somehow brought us here.

I love her school with my whole heart. I always will. Her preschool teachers were some of the first people to notice that something wasn’t right. They saw changes in Brynlee before we had answers. They listened. They cared. I don’t know if they’ll ever truly understand how grateful I am for that.

So this isn’t about not trusting the people she’ll be with.

It’s about learning to trust the world with the little girl I spent over a year fighting to keep in it.

That is so much harder than I ever imagined.

For so long, my job was to protect her from everything I could. Every fever made my heart race. Every appointment felt like it could change our lives. Every single day I knew exactly where she was, because that’s what cancer does to a parent. It teaches you that everything can change in a single phone call.

Now my job is different.

Now my job is to smile when I walk her into kindergarten, help her hang up her backpack, kiss her goodbye, and let her go be an almost six year old.

I hope she falls in love with school.

I hope she finds friends who make her laugh until her cheeks hurt.

I hope she comes home talking about recess, art class, silly stories, and everything in between.

I hope nobody makes her feel different for the parts of her story they can’t possibly understand.

Most of all, I hope that when she walks through those classroom doors, she isn’t carrying the weight of everything she’s survived.

I hope she’s just Brynlee.

Because cancer has already taken enough from my little girl.

This chapter..I pray it gives a little piece of her childhood back. đź©·


Today, we attended Relay for Life, and it was such a beautiful reminder of just how many stories can exist in one place....
08/01/2026

Today, we attended Relay for Life, and it was such a beautiful reminder of just how many stories can exist in one place.

During the survivor and caregiver lap, I carried Brynlee around the park while we walked beside so many people who have fought battles of their own. Survivors, caregivers, families, and loved ones, all carrying memories, fear, hope, grief, strength, and so much love with them.

Looking around, I couldn’t help but think about everything represented in that one lap. Every person there had a reason for walking. Every family had a name, a diagnosis, a story, or someone they wished could have been there beside them. It was emotional, but it was also incredibly beautiful to see so many people come together to honor those still fighting, celebrate the survivors, and remember the ones who are deeply missed.

One of the sweetest parts of the day was sharing it with Kensley and her family. Kensley and Brynlee are both survivors of medulloblastoma, and seeing the two of them together made my heart so full. Two sweet girls who have been through far more than they ever should have, surrounded by people who understood just how meaningful it was for them to be there.

As I carried Brynlee around that park, I felt so proud of her, but I also felt so much love for every person walking beside us. Cancer changes entire families, and days like today remind us that none of these stories should ever be forgotten.

I am so grateful we were able to be apart of such a meaningful day and stand beside so many incredible survivors, caregivers, and families. đź©·





Jada Brooks

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Manchester, MI
48158

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