Trexo Robotics’ cover photo
Trexo Robotics

Trexo Robotics

Medical Equipment Manufacturing

Mississauga, Ontario 7,492 followers

Re-imagining pediatric rehabilitation

About us

Tréxō Robotics is on a mission to redefine mobility solutions for all people. We want to create devices that are designed with the user in mind, and can be used at home. Fundamentally, we are driven by the belief that people should have access to enabling technologies. Currently, we are building a wearable robotic device designed to help children with disabilities experience walking.

Industry
Medical Equipment Manufacturing
Company size
11-50 employees
Headquarters
Mississauga, Ontario
Type
Privately Held
Founded
2016
Specialties
Robotics, Medical Devices, Health & Medicine, Rehabilitation, and Disability

Locations

Employees at Trexo Robotics

Updates

  • View organization page for Trexo Robotics

    7,492 followers

    This video from MaRS Discovery District captures a great snapshot of what Trexo is. Thank you! We are thrilled to be part of the Mobility Unlimited Hub and are grateful for the Toyota Mobility Foundation and their support. MaRS Discovery District we can’t wait to hold our next event in another one of your spaces! We haven’t officially announced it yet, so more details to come soon! Keep your eyes on our social media to learn about our info session and Trexo demo for physical therapists. #marsdiscoverydistrict #mobility #mub #tmf #trexorobotics

  • Congratulations to CHEO for being listed as a Top 40 Research Hospital! We are grateful for the work you do and the difference you make. #CHEOResearch #ResearchHospital #healthresearch

    View organization page for CHEO Research Institute

    9,989 followers

    CHEO is the first acute care pediatric hospital to introduce an implied consent model for its permission-to-contact program to enhance recruitment for studies at the CHEO Research Institute. Called Research Connection, this trailblazing program gives every child, youth, and family who receives services at CHEO the chance to learn about research opportunities at CHEO. “It's incredible how life-changing this research is for kids. It makes such a big difference," said Melanie Radley, mother to four-year-old Hazel who took part in a CHEO research study involving the Trexo Robotics walker. “I feel so much hope for all kids with disabilities."  Learn more about Research Connection ➡️ https://lnkd.in/eGSscxZ9 Thank you to the Ontario Hospital Association for including us in the Top 40 Research Hospital February edition of Health System News. #CHEOResearch #HealthResearch #ResearchHospital H.J. Jardine Jason Berman Jennilea Courtney Lindy Samson Michelle Larin  

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  • View organization page for Trexo Robotics

    7,492 followers

    🎙️ The Mobility Mindset episode 2 is live! 🎙️ Sara & Marc chat with Effie Parks; mom, podcaster and rare disease advocate. 💥 I would say it's passionate and positive while also touching on the feelings of isolation and sadness, as they explore the challenges and joys of raising children with disabilities, discuss the significance of Rare Disease Day, and the vital role of community and connection for parents. Effie shares powerful insights and practical advice from her own journey, offering encouragement to families navigating similar paths. We are grateful Effie could join us - and it was even better than we had hoped for! 💞 Check it out at the link in our comments. Please share or tag anyone you think may be interested. #podcast #trexo #themobilitymindset #onceuponagene #raredisease #rarediseaseday

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  • View organization page for Trexo Robotics

    7,492 followers

    🗓️ Tuesday February 18th, episode 2 drops. Effie Parks shares her insights, energy and has a great conversation with Marc and Sara. Marc and Sara ask important questions and also share their thoughts and experiences. 🥹This is another episode that will really speak to parents, especially ones early in their journey with a kiddo that has a rare disease or disability. 🔗 If you want to share your story, or have a resource or something that will help the families in our community, click the link in comments and submit your request. We will review and get in touch with you! 🎙️ This podcast is in service of our community who are in search of connection, resources and support. Our goal is to create something that may entertain parents, or provide them with new resources or offer inspiration and connection. The possibilities are endless, with the guests we have lined up. 💗 #onceuponagene #raredisease #podcast #themobilitymindset #mobility

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  • I am so excited to share a small clip of The Mobility Mindset episode we just recorded with Effie Parks, (she hosts the Once Upon A Gene podcast). Effie is a long time fan and supporter of Trexo, and we return the love for her and all that she does. This episode is filled with insights into the journey parents go through when their kiddo has a disability or rare disease. The way Sara, Marc and Effie related to each other is exactly why we do this. Parents need support, they need to be seen, they need to see themselves in others. On February 18th this episode drops. We can't wait to hear what you think. There some great tips and resources you will be glad you caught. Link in the comments for our podcast page on our site. I'll also post here the day it drops. - Jenn #podcast #themobilitymindset #trexorobotics #onceuponagene #raredisease

  • View organization page for Trexo Robotics

    7,492 followers

    A mom reached out and shared the following feedback on our first podcast. 🔥 “HOLY SMOKES!! This first episode is so awesome!!!” 👏 🥰 We are grateful for the feedback and kind words. 🎙️If you haven’t checked out The Mobility Mindset yet, we invite you to now. The link is in the comments. 🔗 📆Next episode drops on February 18th and our guest is Effie Parks - mom, advocate, and host of Once Upon A Gene podcast. You won’t want to miss her! 💪If you don’t know Effie, she is a powerhouse who works tirelessly to advocate, share info and resources, help parents with kiddos with rare diseases and more. She’s a wealth of knowledge. I’ll send a reminder so you don’t miss it! 💗 #podcast #themobilitymindset #trexorobotics #onceuponagene #raredisease

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  • The Mobility Mindset with Trexo Robotics is live! Our first ever podcast episode. We are proud of this episode and all that we have planned for the show going forward. Thank you to Sara and Marc for laying it all out there. Your stories matter, they will help other families feel seen, understood and might encourage them to share their stories too. Thanks to Manmeet, who shared his story and then turned the focus on Sara and Marc - while he offered support and compassion. You can find the episodes on Spotify, iHeartRadio, YouTube and Apple. The links are on the page linked in our comments or you can search for The Mobility Mindset and you will find it! Please follow the show, engage with the episodes and share! Our goal is to reach any parents or family members of a kiddo with a disability. We want to support them, share resources and start meaningful conversations. PTs, OTs, and doctors that work with kiddos with disabilities will also be interested in this podcast! We are grateful for shares, comments and likes on this post. If you want to be a guest, click the link in the comments. #trexorobotics #podcast #pediatrics #kidswithdisabilities #pt #physicaltherapist #physiotherapist #themobilitymindset

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  • The Mobilty Mindset podcast launches on Tuesday, February 4th. We are proud of the inaugural episode. The emotion is raw and the conversation is powerful. Our goal with this podcast is to share resources and support for families. Sara & Marc opened up and shared deeply personal details of their stories. The hope is other families will open up and share, maybe not with us, but with someone. The hard conversations can stir up pain, but in the long run, they are important for your mental health. We hope this episode inspires you, and touches your heart. Manmeet also shares his story, which most of us know is so inspirational. Visit our site (link in comments) to let us know if you would like to be a guest on the podcast. You can (and should!) also follow us on your favorite podcast platform. Stay tuned for more details and all links once the first episode is live! #trexorobotics #podcast #themobilitymindset #mobility #disability #ability

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  • To anyone in our community that is in San Diego, check out this event for Rare Disease Day on February 28th. #rarediseaseday #sandiego

    View profile for Effie Parks

    🧬 Host of Once Upon A Gene Podcast 👨👩👧👦 Empowering families navigating rare diseases 🌍 Building a supportive community 🔍 Advocacy | Support | Education 🌟 Subscribe & follow for hope, help & connection

    ✨ It Was Rare & I Was There ✨ Join us on Rare Disease Day - February 28th for an evening of connection, celebration, and community! We’re gathering at Brigantine Portside Pier downtown from 3:30–6:30 PM for food, drinks, music, and rare disease festivities. At the end of the event, we’ll walk across the street for a group photo in front of the San Diego Administration Center, which will be lit up in honor of the rare disease community. 💜 This event is for families, researchers, biotech leaders, and anyone passionate about rare disease advocacy. Let’s come together, share stories, and raise awareness in these precious hours we have together. A huge thank you to our sponsors for making this happen! We are so grateful for your support! 🔗 Tickets are available now—link in comments. Hurry - Space is limited 🦓 E. Gay GrossmanSteve Grossman Jane Maine, CMP LundbeckLa Jolla Labs Inc. PacBio Ultragenyx Fore Genomics Encoded Therapeutics Inc.Trexo Robotics

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  • This platform is such a great tool. When you combine it with working with Advocacy Abby directly, you are armed with the best. Stay tuned for a case study on one Mom’s success in getting her Trexo covered while working with Abby. We have seen parents struggle with funding, not knowing where to turn. We found resources and helped as much as we could. What this platform and Abby offer is next level. Parents now have a place to turn. We are grateful. And we are again reminded of the importance of community. Coming together with people who care and want to help, is how we can all really make a difference in this world. Thank you Abby and Support Now. 💗 #grants #funding #community Connect with Abby or check out the platform and explore it on your own. Link in comments.

    View profile for Jordan Arogeti

    Supporting Supporters I Founder I Investor | Tired Mom

    💡 What if I don’t have a community to lean on? 💡 Are there other ways to cover healthcare costs beyond fundraising? We heard you. With medical expenses on the rise, we know families are looking for real solutions to cover medical expenses without the weight falling entirely on their, or their community’s, shoulders. In partnership with Advocacy Abby (Abby Zachritz) we’ve built Connect, a game-changer for families facing healthcare challenges. 🌍 The largest searchable database of active grants — specifically designed for medical equipment, therapies, and ongoing care. 🔍 Search by location, diagnosis, grant type, and more. 💸 Completely free to use. No strings. No barriers. Whether you're a parent, a PT clinic, a nonprofit, a hospital, or just a caring family member, Connect makes it easier to find the help you need when you need it most. It’s time to change the game for families everywhere. Start exploring grants today. Link in comments. ❤️ #support #familygrants #technology SupportNow Scott Arogeti Morgan J. Lopes

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