Triform Therapy

10/10/2026

Happy birthday to our one and only Blake! We hope you have the best day!

Six years of YOU. Six years of prayers, miracles, overcoming the odds, and witnessing God’s goodness in ways we could have never imagined.

Blake, your story is one that reminds us every single day that God is still in the business of miracles. From your months in the NICU to the countless battles you’ve fought, you have shown us a strength that is beyond anything we could ever put into words. There have been scary moments, hard days, and so many prayers whispered through tears, but God has been by your side through it all. And look at you now, SIX YEARS OLD!

We are SO proud of how far you’ve come. Every milestone, every smile, every laugh, and every little victory means more than most people will ever understand. We know what it took to get here, and we will never take for granted the blessing of watching you grow. You are so much more than your diagnosis or the challenges you face. You are joy, you are light, and you are living proof that God’s plans are greater than our own.

You are a miracle, Blake Garrett, and we thank God every single day that He chose us to be part of your story.

Happy 6th birthday, sweet boy! May this next year bring more smiles, more milestones, more beautiful memories, and countless reasons to praise God. We love you more than words could ever explain!

SIX YEARS OF GRACE. SIX YEARS OF MIRACLES. SIX YEARS OF BLAKE. 🙏🏼💙

“I praise you because I am fearfully and wonderfully made.” — Psalm 139:14 🤍

09/28/2026

✨ We’re growing and looking for the right people to grow with us! 💙💚🩷

Triform is hiring Pediatric PTs, OTs, and SLPs who are passionate about kids, families, and making the impossible feel possible.

⭐ DMI certified? Even better!
🗓️ Full-time OR create a schedule that works for you.

📩 [email protected]

Tri. Transform. Triumph.

09/19/2026

Sometimes the hardest part of being a therapist is not always knowing what a child is capable of until you’re willing to push them to their limit. To challenge them a little more. To believe there might be something in them that even they haven’t discovered yet. Quite frankly, I’m sure some of these parents think we’re crazy and delusional.

Today, we got to watch a child experience walking for the first time. We got to watch “maybe one day” become today. It never gets old… and always stops us in our tracks. How grateful we are to have the privilege of giving him the opportunity to discover what he is capable of.

09/10/2026

💜 **September is STXBP1 Awareness Month, and this one is personal for us.**

Meet our girl, Charlie. 💜

Charlie has **STXBP1 disorder**, a rare genetic neurological condition that affects the way brain cells communicate. In the simplest terms, the messages her brain sends to her body don’t always travel the way they should. Things most of us never think twice about—moving our bodies, communicating what we want, learning a new skill—can require an incredible amount of work for children like Charlie.

Charlie has been part of our Triform family for over three years, both weekly therapy and intensive therapy sessions. We have the privilege of seeing firsthand just how much determination can live inside one little girl.

For Charlie, progress may come through hundreds and hundreds of repetitions. It comes through hard days, tired muscles, frustration, perseverance, and a family that refuses to stop believing in what is possible.

Charlie is strong. She is determined. She is deeply loved. And she has an entire team standing beside her, fighting for every possibility. 💜

This month, Charlie's family is raising money to help support STXBP1 research and the families who are desperately waiting for more answers, better treatments, and ultimately, a cure.

If Charlie's story touches your heart, please consider donating or simply sharing her story. Every dollar, every share, and every person who learns the name **STXBP1** matters.

💜 **Donate in honor of Charlie:**
https://give.stxbp1disorders.org/fundraiser/7499604

Charlie, we are so proud to be a small part of your story. Keep showing the world what's possible. We’ll keep fighting right beside you.

09/04/2026

💙 Every child deserves a voice.

With many of the children we treat, difficulty speaking doesn’t mean they don’t have something to say. AAC (Augmentative and Alternative Communication) gives children a way to share their thoughts, make choices, tell jokes, say “NO,” and communicate like the kids they are.

AAC can also be an important part of intensive therapy, giving children a voice while they work hard toward greater mobility, independence, and participation.

💙 This is our friend Caffrey. Follow his page to see videos of him using his AAC device to communicate like a typical boy would do:
Follow Caffrey’s page⁠

A child who cannot speak clearly still has something to say. Let’s make sure they have a way to say it.

09/01/2026

💙 HELLO, SEPTEMBER 💙

This month, we’re taking time to recognize, educate, and celebrate the incredible children and families whose journeys may look a little different.

Throughout September, we’ll be sharing about diagnoses, disabilities, communication differences, adaptive equipment, and—most importantly—the amazing KIDS behind all of it.

At Triform, we believe a diagnosis can help us understand a child’s needs, but it will never define their potential.

We don’t see children only for who they are today.

We see them for what they can become. 💙💚💗

08/11/2026

🎓 PT GRADUATE ALERT! 🎓

Big cheers for Scottie, who officially graduated from physical therapy at Triform! 💙

We are so proud of all the hard work, determination and progress this little guy has made. Watching our patients grow stronger, gain confidence and reach their goals is one of the very best parts of what we do. Getting a front row seat to all of their hard work makes graduation days extra special! 🥹

Way to go, Scottie! We’ll be cheering you on as you keep moving and growing! 🌟💪

08/04/2026