Mighty Mavs Mission

Mighty Mavs Mission Follow Maverick on his mission with Embryonal Rhabdomyosarcoma. 💙

Tomorrow begins a month that, for most of my life, meant absolutely nothing to me.SEPTEMBER.Childhood Cancer Awareness M...
09/01/2026

Tomorrow begins a month that, for most of my life, meant absolutely nothing to me.

SEPTEMBER.

Childhood Cancer Awareness Month.
I saw the gold ribbons. I saw the posts. I knew children got cancer, but I never really stopped to understand it. Because you never think it will be your child. You never think it will be your family sitting in a room listening to a doctor say words you can barely comprehend because the only word your mind can hear is “cancer”. You never think you will learn the names of chemotherapy drugs instead of new toys. You never think you will know what a port is, what blood counts need to be, what scans are looking for, or how quickly a fever can turn into a medical emergency. You never imagine watching a tiny child endure things that would bring most adults to their knees.

Until childhood cancer has a name.

A face.

A laugh.

A favorite toy.

A little hand you have held.

And suddenly, that gold ribbon means everything.

For us, childhood cancer has a name.

Maverick.

And now I understand why September matters.
Childhood cancer needs to be recognized because these aren't just statistics. They are babies, toddlers, children and teenagers who should be worrying about scraped knees, cartoons, school, birthday parties and what they want to be when they grow up. Their parents should be planning vacations and first days of school, not treatment schedules. Their grandparents should be spoiling them, not begging God to let them take their place. Their childhood should not include chemotherapy, surgeries, radiation, ports, scans, transfusions, hospital stays and words no child should ever have to know.

And yet, for far too many families, it does.

Before cancer touched my family, I could scroll past a childhood cancer post and feel sad. Now I know there is an entire world behind those posts. There is a mama lying awake at 3 a.m. listening to her child breathe. There is a dad trying to hold his family together while he is terrified too. There are siblings whose lives change overnight. There are grandparents praying prayers they never imagined they would have to pray. And there are families carrying an unimaginable grief because childhood cancer took what should never have been taken.

That is why we need to talk about childhood cancer. Not because we want sympathy. Not because we want people to feel sorry for us. But because awareness matters. Research matters. Funding matters. Treatments that are safer and more effective matter. And every single child fighting deserves to know that the rest of us are willing to fight for them, too.

So this September, when you see a gold ribbon, please don't just scroll past it.

Stop for a second.

Say the child's name.

Share their story.

Pray for them.

Support their families.

Donate to childhood cancer research if you are able.

Wear gold.

Ask questions.

Learn about it.

Talk about it.

Because childhood cancer may not be part of your world today, & I pray with everything in me that it never is, but these children need people to care before it becomes personal.

I wish I had understood that sooner.

This September, I will wear gold differently.

I will see every gold ribbon differently.

Because now, when I look at that ribbon, I don't just see childhood cancer.

I see Maverick.

I see his courage.

I see his fight.

I see every child fighting beside him.

And I see every reason in the world why we cannot look away.

September is Childhood Cancer Awareness Month.

Go gold. Speak their names. Share their stories. Pray without ceasing. Fight for better treatments. Fight for more research. Fight for every childhood cancer family.

Because kids deserve to grow up.

And until every child gets that chance, gold deserves to be seen.

🎗️ Team Mighty Mav 🎗️

No child should have to fight cancer. But every child who does should have an army standing behind them.

We haven’t updated on Mav much lately because there hasn’t been much to update on, which we’re so thankful for! Mav is d...
08/06/2026

We haven’t updated on Mav much lately because there hasn’t been much to update on, which we’re so thankful for! Mav is doing so well through maintenance chemotherapy and we are working on month 5 with only 7 more weeks to go until he’s finally finished with treatment! After treatment, he’ll get one more set of scans & then, by the grace of God, he will be declared NED (No Evidence of Disease)!

Continue to pray that he handles maintenance well & we make it to the end of this with clear scans! He is small, but he is mighty! He is 🩵

Prayers for Mav are greatly appreciated! He’s been admitted due to cellulitis in his ear, probably caused by a mosquito ...
06/29/2026

Prayers for Mav are greatly appreciated! He’s been admitted due to cellulitis in his ear, probably caused by a mosquito bite or some other type of bite. Their plan is to run antibiotics overnight and manage the swelling of his ear. We’re hoping for just a 24 hour stay! Pray that the meds work wonders & get our boy back to normal! 💙💪🏼

Tomorrow is scan day for Mav! Pray he still has clear scans & no tumor growth! Also throw a prayer in for his daddy & I,...
06/23/2026

Tomorrow is scan day for Mav! Pray he still has clear scans & no tumor growth! Also throw a prayer in for his daddy & I, scanxiety is brutal😵‍💫🥲 We also start cycle 4 of maintenance Thursday, so only 2 more to go after that! 🙌🏼

As always, he’s small, but he’s mighty! He’s ! 💙💪🏼

We got Mavs first survivor box from St. Jude today. 💛🎗️It’s so crazy how it’s been over a year now and the scary & hard ...
05/27/2026

We got Mavs first survivor box from St. Jude today. 💛🎗️

It’s so crazy how it’s been over a year now and the scary & hard stuff is nothing but a memory. We are so thankful that God carried our sweet boy through that deep valley and brought him out in a better one! We owe Him all the glory!

Mav is set to start cycle 3 of his maintenance tomorrow, & he is taking each dose so well! Only 3 more to go after this one! He’s also even almost completely potty trained! 🙌🏼

We ask that you continue to pray for Mav & our family as we navigate through the rest of treatment. We love you all so much & we’re thankful for each of you!

One whole year of St. Jude 💛🙌🏼First pic is from our very first time through the doors & the second is today before blood...
04/30/2026

One whole year of St. Jude 💛🙌🏼

First pic is from our very first time through the doors & the second is today before bloodwork! Ain’t He good yall? I just can’t stop praising Him for bringing my baby through this! 😭🙌🏼

Hey guys! We haven’t updated on our super hero in a while, so I figured today would be a good day to do so! Maintenance ...
04/23/2026

Hey guys! We haven’t updated on our super hero in a while, so I figured today would be a good day to do so!

Maintenance Chemo is going so good! No side effects or symptoms! & Mav has been feeling GREAT! 🙌🏼 We met with his new pediatrician today & had bloodwork done closer to home instead of all the way in Memphis, so we’re thankful for a shorter drive 😌 Everything went well at his appointment & he’s gaining weight & his hair is growing back yet again, hopefully to stay this time! 🥰

Continue to remember him as he goes through maintenance and as we adjust to having a pediatrician now instead of just our doctors at St. Jude. We love you guys & can never thank yall enough for yalls prayers! 💛🎗️

Big day for Mighty Mav! 💛🎗️💪🏼 Remember us today as Maverick starts maintenance chemo! Pray that the side effects are min...
04/02/2026

Big day for Mighty Mav! 💛🎗️💪🏼

Remember us today as Maverick starts maintenance chemo! Pray that the side effects are minimal & he handles this treatment like a pro just like the rest 🤪
We love you guys so much!

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Falkner, MS

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