Caysens Crew Inc.

05/06/2026

Camdyn is sharing how he makes his gluten free waffles in the morning using his dedicated gluten free toaster 🫶🏻

04/28/2026

Sharing Caysen’s story and this is just the beginning 🫠 It’s important to note that even through all of his toughest days, this little boy remained strong every step of the way. He is a true fighter and continues to conquer.

My hopes in sharing is to help raise awareness not only around the existence of different medical diagnoses and complexities, but to spread light on everything families face while enduring such a challenging journey.

Part 1 of Caysen’s journey can be heard here…stay tuned for part 2.

04/27/2026

Having a medically complex child is something a parent simply cannot describe. Unless you’ve faced it, you don’t fully understand. Hearing the words “your child may never walk” hits harder than you can imagine. Constantly questioning what you did wrong or even what you didn’t do. Unsure where to turn next or what “surprises” are around the corner as you watch your child endure some of the most intense moments. Wishing you could take their place but knowing you can’t. Today, we are thankful for so many things. For having a medical system that is lifesaving to many. Medical equipment to take over when our bodies need the extra help. Having the skilled and nurturing hands of many nurses, doctors, surgeons, patient care techs, etc all in one place to assure your child receives the top notch care you’re praying for. Seeing your children reunite after months of hospital stays and so much time apart. And then seeing your child not just walk but RUN with all their being after fearing the worst. I can’t help but be thankful for everything. Hallelujah.

Justin Bieber Hailey Bieber

04/24/2026

You saw his story… but here’s what daily life really looks like.

Caysen doesn’t just “have a diagnosis.”

He lives with:
🫁 A lung condition that makes it hard to clear mucus
🧠 A brain condition that required surgery
🍽️ A feeding disorder that requires a G-tube
💊 Daily medications and airway treatments

What most people don’t see:
➡️ Treatments every day just to breathe
➡️ Monitoring for infections that can escalate quickly
➡️ Appointments, therapies, and constant vigilance

There are no “days off” from this life.

And yet…

He still laughs.
He still plays.
He still shows more strength than most adults ever will.

💙 This is why we share his story.
💙 This is why awareness matters.

Every appointment.
Every procedure.
Every day… comes with a cost.

But more importantly—
it comes with a purpose.

✨ To raise awareness
✨ To support research
✨ To help families navigating rare diseases

If Caysen’s story moved you, we ask for your support.

💙 Donate
💙 Share
💙 Help us spread awareness

Together, we can make a difference.

04/07/2026

There are moments in life that split your world into before and after.

For us, it began the day Caysen was born.

What should have been a joyful moment quickly turned into fear as his oxygen levels dropped dangerously low… and our newborn was rushed away, fighting to breathe. That was only the beginning.

At just a few months old, Caysen was in and out of the hospital battling infections that wouldn’t go away. Eventually, we learned he was living with a rare genetic condition — Primary Ciliary Dyskinesia — making even something as simple as breathing a daily challenge.

Then came the seizures.
Then the MRI.
Then the words no parent is ever prepared to hear…

Brain malformation.
Hydrocephalus.
Emergency surgery.

At just 1 year old, we handed our baby over for brain surgery — not once, but three times.

We lived in the PICU.
We watched him endure unimaginable pain.
We faced complications, feeding tubes, and diagnoses we had never even heard of.

And yet…

Through it all, Caysen smiled.
He fought.
He showed us what true strength looks like.

Today, Caysen continues to face challenges — from a VP shunt to feeding struggles to Eosinophilic Esophagitis — but he keeps pushing forward with a resilience that inspires everyone who meets him.

And it’s because of him… that Caysen’s Crew was born.

We created this nonprofit so no family walking a complex medical journey feels alone the way we once did. We provide support, financial assistance, and hope to families who are in the fight of their lives for their children.

Because we know what it feels like to sit in that hospital room.
We know the weight of medical bills, fear, and exhaustion.
And we know how much it means when someone shows up for you.

This Arizona Gives Day, we’re asking you to stand with families like ours.

💛 Help us continue supporting children like Caysen
💛 Help us ease the burden for families in crisis
💛 Help us turn pain into purpose

If Caysen’s story touched your heart, please consider donating or sharing:

https://square.link/u/K8Cx2sSV

Together, we can remind families that they are not alone — and that even in the hardest moments, there is still hope.

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04/03/2026

What if $25 could change TWO lives… yours and a family in need? 💛

Right now, we’re pushing hard to sell out our 100 Jim Click Millions for Tucson raffle tickets… and we’re not there yet.

We’ve sold 11.
That leaves 89 tickets still waiting for someone to say YES.

But this isn’t just about a raffle…

This is about the mom sitting in a hospital room wondering how she’s going to pay bills.
This is about the child facing procedures no child should have to go through.
This is about families who feel completely alone—until someone shows up.

That someone is Caysen’s Crew.
And right now… we need YOU to help us keep showing up.

✨ Your $25 ticket could win you:
🚗 A brand new 2026 Nissan Frontier
✈️ A dream vacation anywhere in the world
💵 $5,000 cash

…but more importantly…
👉 it helps us support families in the middle of real, raw, life-changing moments.

💥 We can’t get more tickets until these 100 are gone.
So every single share, every single purchase matters.

🎟️ $25 each or 5 for $100
👇 Buy here:
https://square.link/u/gCXbpf4i

If you’ve ever thought… “I wish I could help”
👉 This is your moment.

And if you can’t buy right now, please share this post—you might be the reason the right person sees it.

Let’s sell these out together.
Let’s show families they are NOT alone 💛

Comment ‘DONE’ when you grab your ticket so we can thank you 💛

- Caysen’s Crew

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04/01/2026

Please help Caysen by voting for him to become the next Jr Ranger!!! You get 1 free vote every 24 hours! Please vote and share asking others to vote too 🫶🏻❤️🫶🏻❤️

Caysen Is A Warrior! Even While Facing A Tough Medical Journey, He Continues To Play And Explore Just As Any Child Should!

03/28/2026

🚨 We’re so close… but we need your help! 🚨

We’ve officially sold 11 out of 100 raffle tickets for the Jim Click Millions for Tucson giveaway… and every single ticket is helping us support families walking through some of the hardest medical journeys imaginable 💛

But here’s the catch…
👉 We need to sell ALL 100 tickets before we can get more.

That means 89 tickets to go — and we can’t do it without YOU.

✨ When you buy a ticket, you’re not just entering to win:
🚗 A brand new 2026 Nissan Frontier
✈️ Dream vacation anywhere in the world
💵 Or $5,000 cash

…you’re helping Caysen’s Crew continue showing up for families who truly need it.

These families are juggling hospital stays, diagnoses, financial stress, and uncertainty. And because of YOU, they don’t have to do it alone.

💥 Let’s sell these 89 tickets together 💥

🎟️ $25 each or 5 for $100
👇 Grab yours here:
https://square.link/u/gCXbpf4i

Even if you can’t purchase, sharing this post means everything to us.

We’re building something bigger than a fundraiser…
We’re building hope 💛

— Caysen’s Crew

03/15/2026

What local Tucson businesses would you recommend reaching out to to request event sponsorships and/or in-kind donations?

Currently planning our annual Boot Scoot & Boogie event and could use the community’s help 😅