Canadian-made exoskeleton helps kids with health challenges walk, but price is a barrier

Max Labelle’s face lit up the first time he tried out a Trexo Robotics exoskeleton. At just four years old, Max was born with hypotonic cerebral palsy, a condition that affects the stability of his muscles, making basic movements like sitting, standing, and walking challenging. The exoskeleton proved to be a game changer for Max, providing support for his torso and helping him lift his legs as he practiced taking steps during physiotherapy sessions.

However, accessing the exoskeleton was not an easy task for Max and his family. They had to travel from Maple Ridge, B.C., to the Canadian Centre for Development in Calgary, one of the few places in Western Canada that had the device. Despite the distance, Max’s mother, Jamie Labelle, noticed significant improvements in Max’s posture and leg usage within just a week of using the exoskeleton.

The excitement of seeing Max benefit from the exoskeleton was quickly overshadowed by the hefty price tag of $40,000, which was not covered by public health insurance. Labelle described the cost as a “gut punch” and turned to online fundraising to help cover the expenses. Many families facing similar situations have resorted to crowdfunding to afford the life-changing device.

Time is of the essence for children like Max, as early intervention is crucial for their development. Julie Rubin, the executive director of the Canadian Centre for Development, emphasized the importance of providing support to children with cerebral palsy at a young age to maximize their abilities in the future.

Despite the financial challenges, families are determined to provide their children with the best possible care. Trexo Robotics, the company behind the exoskeleton, acknowledges the high cost of the device but recognizes its transformative impact on families. Marc Robert, Trexo’s customer success manager, shared his own experience of fundraising for his son’s exoskeleton, highlighting the device’s ability to improve daily activities like grocery shopping.

For Max’s family, the initial shock of the exoskeleton’s price has not deterred them from pursuing the device for Max. Through ongoing fundraising efforts, they have made significant progress towards their goal. Jamie Labelle expressed her determination to continue raising funds until they can afford the exoskeleton for Max.

The journey of Max and his family reflects the challenges faced by many families navigating the costs of specialized medical equipment. Despite the obstacles, their resilience and determination to provide the best care for Max showcase the power of love and community support in overcoming adversity.