Trexo Robotics

03/10/2026

Bringing world-class mobility right into your living room. 🏠🤖

Movement should be a part of a daily routine, not just a weekly therapy appointment. For children with Cerebral Palsy (GMFCS III-V), SMA, Spinal Cord Injury, and other neuromuscular conditions, the Trexo Home provides an opportunity to stay upright and active in a familiar environment.

This technology turns your living space into a place for weight-bearing and over-ground walking, allowing robotic movement to fit seamlessly into your family’s everyday life. It is designed to help kiddos with mobility challenges experience the world from a standing perspective whenever they are ready to move.

If you are wondering if Trexo is right for your kiddo, fill out the form at the link in our bio.

03/08/2026

To all women, across every field and every border: your vision defines our progress.

On International Women’s Day, we celebrate the incredible contributions of women everywhere. From medicine and engineering to education and advocacy, women are the driving force behind the world's most critical advancements.

Today we honor your brilliance, your grit, and your unwavering commitment to building a better world for everyone.

Happy International Women’s Day to every woman making the impossible a reality, from all of us at Trexo.🥹🐾

03/05/2026

Our mission has no borders because every child deserves the chance to walk. 🌎✨

From launching in Australia and Hong Kong to connecting with families at conferences in Dubai and beyond, it’s been a whirlwind of a year. But we aren’t slowing down, our team is headed to Spain this month! 🇪🇸

The goal has always been simple: expand our reach so that every kiddo who needs a Trexo has the access to get one. Whether it’s through new launches or global partnerships, we are committed to bringing life-changing mobility to every corner of the world.

We’re expanding because our community is growing. Tag a family or a clinic in Spain who needs to know we’re coming, or drop a comment with the country you want to see us visit next!

03/05/2026

You go little champ 🐾
You are doing so well 🙌🏼

03/04/2026

This technology is redefining what movement looks like for kids with mobility challenges. 🤖👇

Watching this technology move on its own is a glimpse into the future of mobility. It is designed specifically to help children with mobility challenges navigate the world in an upright position. This robotic system supports kiddos with a wide range of diagnoses, including Cerebral Palsy, Spinal Cord Injury, Stroke, and other neuromuscular conditions.

By using robotics to assist the body, we can bridge the gap between sitting and walking, creating new opportunities for exploration. This innovation is about giving every child a chance to walk, regardless of their diagnosis, the chance to experience the world from a standing perspective.

How to connect 👇
👋See if Trexo aligns with your child’s height and mobility needs. Fill the form, link in our bio.

👋Follow Us: Join our community to see the journey unfold and learn more about mobility solutions.

03/03/2026

We know that choosing the right technology for your child’s journey is a big decision.

What questions do you have for us about the Trexo Treadmill?

Drop them in the comments below! 👇

03/03/2026

A moment of pure wonder reflected on every face; the parents, and even Marc and Rukaiya's from the Trexo team.

03/02/2026

03/02/2026

Kendrick is ready for a new week in his Trexo 💕🥹

03/01/2026

More smiles. More milestones. More movement. ✨

Every day at Trexo, we are driven by the hope and resilience of the families we serve. Our mission is global, our team is growing, and our vision is clear: we won't stop until this technology reaches every family who needs it.

Your support is the engine behind our innovation. Thank you for being with us every step of the way.

DM us if you have any questions or leave them in the comments below ⤵️

03/01/2026

🚨 Monday just got a million times better 🚨

Baby Marley dropped the most precious video on us saying "I am walking backwards, Dada" 🥰💕🤗

This little human just reminded us that progress doesn't always look like moving forward - sometimes it's about mastering those backward steps.

🫠Who else is absolutely MELTING right now?

Curious about Trexo? Send us a DM and let's chat!⤵️

02/28/2026

The joy, the "fumble," and the visibility of rare families.

Today is Rare Disease Day. 🦓 In our community, "rare" isn't just a medical category,it is a lived experience of grit, laughter, and a different kind of magic.

Today, we are honored to share Ford’s story, exactly as written by his mom:

“Ford wakes every morning and with a grin, asking for his Gaga and teases me by hiding under his blankets. He is 9 years old and was born with CTNNB1 syndrome, an ultra-rare genetic disorder that touches 550 kids worldwide, Ford navigates a world that didn't quite build paths wide enough for his wheelchair or words soft enough for his triumphs. Doctors once whispered limits with a that is uncertain. But Ford? He listens to his own rhythm. With fierce love from his family and friends cheering every milestone, he pedals his adaptive bike like it's a rocket ship, squeals and wheels his wheelchair and Ford Loghtning, ask his dad to kick the football on the roof and taunts him with "fumble!" If he misses. He lights up rooms with laughter that saves our family every day. ] For Rare Disease Day, Ford's story reminds us that community saves, telling your story helps move research, and that living in the moment is such a gift and is critical to living and loving this life. One gene changed eve”

To our families navigating rare genetic journeys: We see you. We see the kids who rewrite the rules of physics and the parents who build the paths the world forgot to pave. You are the heartbeat of Trexo. We see your fight, we celebrate your "fumbles," and we are so proud to be in your corner.