PROUD TO SUPPORT Kim S RECIPIENT 3RD QUARTER 2024

Kirista Beckett • August 14, 2024

Brokers Who Care voted and we are pleased to announce that we will be sending a cheque in the amount of $10,000 to Kim S, our Recipient of the 3rd Quarter 2024 vote.


Thank you Sabeena Bubber for bringing this Cause to our attention.


Their Story:
Kim is a member of our mortgage family. She was trying to get a divorce and her ex husband tried to kill her because of it. In the process, when he fled, he took his own life. Kim is trying to pick up the pieces for her and her 3 daughters they shared. With the ex now being deceased she has no financial support in the way of child or spousal and now has to battle his executor to divorce from his estate and get what’s rightfully hers and the girls. She has two attorneys she has to pay; a divorce attorney and an estate attorney. He was the primary income earner. Her ex-mother in law is blaming her for his death and does not want her to receive the funds. She is also looking at having to go for reconstructive surgery for the nerve damage in her face plus counselling for the children all while being self employed and supporting three young girls. There has been an outpouring of support from many people in our industry. Let's show her that Brokers Who Care will help her to get through.

By Deploy.Mortgage April 10, 2026
Your credit score is one of the most important numbers in your financial life — especially when it comes to getting a mortgage. But for most Canadians, how that number actually gets calculated remains a bit of a mystery.
By Brokers Who Care February 16, 2026
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.
By Brokers Who Care February 16, 2026
Brokers Who Care voted and we are pleased to announce that we will be sending a cheque in the amount of $10,000 to Lisse's Family Fighting for Healing and Stability our Recipient of the 1st Quarter 2026 vote. Thank you Lauren Sbitney for bringing this Cause to our attention. Lisse and her husband Zach are facing an urgent crisis after Lisse was diagnosed with aggressive MS that threatened complete paralysis. In January 2025, emergency hospitalization revealed major spinal lesions, and she was told she could lose all mobility within months. Desperate to save her life and health, they drained their life savings and fundraised to pursue a stem cell transplant in Mexico. While the treatment has halted the disease's progression, recovery requires one to two years of intensive care and therapy. Eight months in, Lisse continues to make slow gains alongside expected setbacks. With Zach unable to work since December 2024 to care for both Lisse and their 10-month-old daughter Effie, the family is drowning in mounting debt despite living on an extremely tight budget. Their income-assistance application is still pending after six months of waiting.  They urgently need support to access therapies that could meaningfully accelerate Lisse's healing and provide their family with basic stability. Your help would ease their financial burden and allow them to focus on recovery and giving Effie the secure childhood she deserves.
Show More