Brokers Who Care voted and we are pleased to announce that we will be sending a cheque in the amount of $10,000 to Lawson-Needs Our Help our Recipient of the 1st Quarter 2026 vote. Thank you Emily Miszk for bringing this Cause to our attention. About a year ago, what appeared to be a routine illness became a life-threatening crisis. Lawson developed massive blood clots, and during a procedure, his heart stopped. He went without oxygen for up to 45 minutes and required CPR and ECMO life support to survive. Against incredible odds, Lawson is still here. He is now off life support, but he sustained significant brain injury. His recovery requires ongoing, intensive therapy, specialized care, and long-term medical support. Before this, Lawson was an active, sports-loving kid, often found at the rink supporting his older brother Cooper—a team captain who continues to show remarkable strength and leadership through it all. Today, Lawson’s family is navigating time away from work, ongoing medical travel, and the emotional and financial weight of rebuilding their lives around his recovery. Your vote is more than financial support—it’s access to therapy, care, and the opportunity for Lawson to reach his fullest potential. Lawson has already shown incredible strength. With our support, his story can continue to be one of resilience, progress, and hope.

Brokers Who Care voted and we are pleased to announce that we will be sending a cheque in the amount of $10,000 to Let's Cure Lucas - Fighting an Ultra-Rare Genetic Disease our Recipient of the 1st Quarter 2026 vote. Thank you Rocco Mongelli for bringing this Cause to our attention. Lucas Azevedo is a four-year-old with an ultra-rare gene variant affecting the RBM28 gene—a condition so rare that only one other child in the world has been discovered with it. This disease is currently unnamed and has no cure, but his smile and spirit inspire everyone around him.  Lucas lives with significant physical challenges. His ultra-rare gene variant affects all four of his limbs, his balance and coordination, his speech, his oral strength, and much more. His muscles are both tight and fragile, making even the simplest movements a challenge against gravity itself. Nothing happens automatically for him—every movement requires intention, strength, and support. The RBM28 variant affects his cerebellum, the area of the brain vital for coordinating voluntary movements, balance, posture, and motor learning. While there is currently no cure, gene therapy has been developed and has proven successful in stopping progression for many ultra-rare diseases. Lucas's family is hopeful about ongoing research and potential breakthroughs. In the meantime, Lucas works incredibly hard six days a week undergoing physiotherapy, occupational therapy, speech therapy, swallowing therapy, and hydrotherapy to build strength and independence. His goal is to walk independently, run, jump, and ride a bike. Your support directly funds the therapies and care that allow Lucas to keep fighting and growing stronger. Together, we can help this remarkable little boy achieve his dreams and contribute to the research that may one day lead to a cure. Thank you for standing with Lucas and his family in this urgent fight.