In this episode, we sit down with Nitin Ambardar and Angus MacKay, clinic owners with Kids Physio Group, to talk about their journeys in pediatric physiotherapy and the impact of introducing Trexo into their clinics.
They share what inspired them to specialize in pediatric physiotherapy, why they chose to bring Trexo into their practice, and powerful stories of children taking their first steps with this technology. You’ll also hear their thoughts on creating fun, family-centered clinics, supporting kids with complex neurological needs, and leading teams that keep care both innovative and approachable.
This is a must-listen for parents, therapists, and anyone interested in the future of pediatric physiotherapy, child mobility, and assistive technology.
In this episode, we’re joined by Tracy Collier, Executive Director of Ontario Track3 Adaptive Sports Association. Tracy’s journey with Track3 started as a supporter, but it quickly became deeply personal when a young family member with cerebral palsy joined the program - and learned to ski before he could walk.
Tracy brings over 20 years of leadership experience and a passion for creating inclusive spaces where children with disabilities can thrive.
We talk about:
The transformative power of adaptive skiing and snowboarding
What inclusive sport really means for families
How Track3 builds confidence, connection, and independence through movement
The personal side of leadership - balancing career, motherhood, and mission
Why early access to adaptive sport matters more than ever
Whether you're a parent, therapist, educator, or someone who believes in making the outdoors accessible to everyone - this conversation will leave you inspired.
🎧 Follow the podcast and stay tuned for more stories at the intersection of mobility, innovation, and inclusion.
In this powerful episode, we sit down with Billy, co-founder of BILLY Footwear, to explore how he transformed personal adversity into a global mission of inclusion. Billy shares the story behind his adaptive shoe brand, the challenges of designing for accessibility, and how he's reshaping the future of fashion—one foot at a time.
Follow and share if Billy’s story inspires you. It definitely inspired us.
#Inclusion #AdaptiveDesign #BillyFootwear #DisabilityAdvocate #Entrepreneurship #Motivation #Paralysis #AccessibleFashion #FounderStory
In this episode, we’re joined by Kiran Mann, Chief Happiness Officer of M2M Business Solutions Inc. and CEO of Brar’s, to explore how joy, resilience, and visionary leadership can transform businesses from the inside out.
Kiran introduces us to her powerful frameworks: The Happy Organization (THO) and the JOY Movement (Just Overcome Yourself). Voted one of the Top 10 Most Inspiring CEOs and a Woman of Influence, Kiran shares her wisdom on how to build cultures that thrive through change.
Brar’s is proud to partner with Trexo Robotics in a shared commitment to supporting our community and driving meaningful impact together.
In this impactful episode, we speak with Brenda Agnew — parent and family advocate, Marketing Director at Gluckstein Lawyers, and mother to two sons, including Maclain, who has severe Cerebral Palsy and profound hearing loss caused by Kernicterus, a rare but preventable brain injury from untreated jaundice.
Brenda shares her journey navigating the complex worlds of healthcare, special education, and disability services, while becoming a powerful voice for families of children with neurodiverse needs.
💬 Topics We Cover:
Living and parenting with a child with disabilities
Advocating for children with complex medical needs
Building inclusive systems in education and healthcare
Brenda’s leadership as a school board trustee and Chair of the Special Education Advisory Committee
🌟 Why This Episode Matters:
If you’re a parent, educator, healthcare professional, or disability ally, this episode offers valuable insights into real-world advocacy, system change, and building inclusive communities. Brenda’s story is one of resilience, empowerment, and creating space for every voice to be heard.
🔔 Follow for more episodes on disability advocacy, parenting children with special needs, and inclusive policy-making.
In this episode, we talk with Parag Gad, neuroengineer and CEO of SpineX Inc., about the future of neurorehabilitation and mobility innovation. With 17+ years of experience in spinal cord research and bioelectric medicine, Parag shares how his transition from academic research to medtech entrepreneurship is driving real-world impact. He dives into the science behind SpineX’s non-invasive neuromodulation device — and how it's helping individuals with spinal cord injuries, stroke, and cerebral palsy regain mobility. Discover how cutting-edge spinal stimulation is unlocking new possibilities in neurological recovery.
In this episode, Dr. Elizabeth Condliffe, a leading expert in neurorehabilitation and pediatric-onset disabilities, discusses how robotic gait training with the Trexo is changing outcomes for individuals with cerebral palsy and other mobility impairments. Backed by clinical research and real-world case studies, Dr. Condliffe shares insights into assistive technology, neuroplasticity, and the impact of robotics in physical therapy.
Whether you're a clinician, caregiver, researcher, or simply curious about the future of mobility and disability innovation, this conversation offers powerful insights into what's possible when research meets real-world impact.
In this episode, we sit down with Eric Jorgensen, an expert in disability planning, whose decades of experience have helped families navigate the complexities of public benefits, financial strategies, and long-term support for individuals with disabilities. As the Director of Special Projects at the First Maryland Disability Trust, Eric shares how he bridges the gap between legal tools and the real-life needs of families. We explore his journey—from serving in the Navy to becoming a devoted caregiver and a dedicated advocate. Whether you're a parent, professional, or planner, this conversation offers valuable insights!
In 2021, Navi’s life changed dramatically after a diagnosis of Guillain-Barre Syndrome (GBS), a rare neurological disorder that led to paralysis. Over the years, Navi has shown remarkable progress in recovery, transitioning from a wheelchair to using a walker and crutches with AFO braces, despite ongoing challenges with partial paralysis in the legs and feet and limited fine motor skills in the hands.
Before GBS, Navi thrived on an active lifestyle, frequenting the gym daily—sometimes twice a week—and finding solace in running as both therapy and exercise. Losing that freedom was a profound challenge, yet Navi remains determined to embrace life fully, facing each day with unwavering resilience.
This episode features Jaime Labelle, mom of 2 boys - one of them a CP warrior and Trexo user. She talks about juggling all the balls and what happens when you feel like you've dropped a ball. Her, Marc & Sara (hosts) chat about real life and that you can't control it all. Perfect example - a plumber showed up at Jaime's house while recording the episode. We easily edited that out of the podcast - but you can't always edit things out of real life!💞
Jaime's reason for coming on the podcast, in her words: "This road can be lonely and I want to help change that."
Tune in to listen to Jim, former NHL player with the Calgary Flames, Stanley Cup winner, Olympian, and Chairman at Properly Investment Company. Listen to him discuss his experience as a grandparent to a kiddo with a rare disease (and a little hockey talk). Some very interesting conversations!
Abby, known as Advocacy Abby shares her story, and talks about how she can help families get the support they need to find financial resources. She offers solutions that help take the burden off parents who are going through it alone with searching for financial resources and funding options. Abby is a friend of Trexo, and we are thrilled to work with her! Let us know what you think about this episode!
It's Cerebral Palsy Awareness Month! In this inspiring episode, we dive into the remarkable journey of the Mertens family. Alex, who has cerebral palsy, opens up about her personal challenges and triumphs, sharing her experiences with Trexo and the impact it's had on her life. Her mom, Carol, and her sister, Katie, also join the conversation, offering their unique perspectives on the family’s journey. Tune in for an uplifting conversation!
Instagram: @thealexscoop
https://thealexscoop.com/
Trexo CEO and co-founder Manmeet Maggu sits down with Liberal Leader candidate and Canadian businessman Frank Baylis. They discuss medtech and innovation, healthcare in Canada, Frank's history, the fascinating story of his mother and more. An open and interesting conversation.
Hosts Sara Valenzuela and Marc Robert engage in deep conversations with Effie Parks, podcaster and advocate for rare disease. They discuss the challenges and joys of parenting children with disabilities, the significance of Rare Disease Day, and the importance of community and connection among parents. Effie hits on some key points for parents and shares advice based on her experience.
In part 2 of episode 1, Sara opens up about her incredible journey, sharing the challenges she faced from her time as a cop in the U.S. to her battle with cancer, and the difficulties she encountered with childbirth. Her story is one of resilience, strength, and determination. This powerful and emotional episode is a reminder of the strength we can find in ourselves even during the darkest times.
In this episode, Manmeet and Marc discuss their paths leading up to and during their time at Trexo Robotics. Manmeet reflects on the challenges of failed prototypes and the dedication it took to become the CEO of Trexo Robotics, bringing the Trexo to life. Marc also shares his personal story of raising a child with a disability and how that journey led him to become a sales specialist at Trexo Robotics.
Don’t miss part 2 of this episode, where Sara shares her deeply emotional story—make sure to have some tissues nearby!
