Brokers Who Care voted and we are pleased to announce that we will be sending a cheque in the amount of $10,000 to Chico - Battling Cancer our Recipient of the 2nd Quarter 2026 vote. Thank you Rosa Bovino for bringing this Cause to our attention. Chico is a loving husband and father who has always given back to his community, family, and friends. His life changed unexpectedly when he suffered a sudden seizure and was diagnosed with an inoperable brain tumor. His family has stood by his side through every challenge, and he has been unable to work due to his condition. Despite exhausting all conventional treatment options, there is still hope. Optune Gio is a device that could slow the tumor's growth and give Chico more precious time with his loved ones. However, the cost of this life-extending treatment is overwhelming, and his family urgently needs support to afford it. Chico's journey has been incredibly tough, but the community has rallied around him. Your support, no matter the size, will go directly toward his care, easing the financial burden on his family during this difficult time. Together, we can help Chico access the treatment he needs and allow him to focus on what matters most—spending time with the people he loves. Thank you for your kindness and generosity during this critical time.

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.