PROUD TO SUPPORT SAVING SAVANNA – RECIPIENT FOR 1ST QUARTER 2020

100Brokers • March 10, 2020

100Brokers Members voted and we’re very pleased to announce that we will be sending a cheque in the amount of $10,000 to Saving Savanna, Recipient of the 1st Quarter vote of 2020.

Savanna was born on April 11, 2018. She is beautiful, sassy, spirited, warm, loving, funny, challenging and strong willed.

Savanna is a little girl who went from “normal” to “stage 4 Neuroblastoma cancer”. She is fighting the fight of her life at the tender age of 22 months. Her parents want to comfort her and spend as much time with her as they can.

Thank you to Lana Russell for bringing this Cause to our attention.

Nomination Story
Monday, January 13, 2020, Savanna’s parents noticed that her tummy was distended a little to the left, which seemed a bit off, but she was playful and happy, so they were not too worried. She had a history of irregular bowel movements. Tuesday she had been out with her daddy and her brother’s for what was a normal day for her, but post nap her tummy was clearly bothering her. Savanna slept a little extra Wednesday morning. When she got up she was walking a little funny and still bloated to the left, so off to the doctor’s office they went.

The doctor felt and listened to her tummy and thought, similar to her parents, that it could be a bowel obstruction? Her bowels seemed slow moving, so off to pediatrics at Ridge Meadows Hospital in Maple Ridge Savanna was sent for an x-ray, blood work and possibly an enema. The x-ray returned and it was not an obstruction, but there was clearly a mass. The blood work came back with signs of swelling and low hemoglobin so they were sent to Children’s Hospital in Vancouver that same day by ambulance.

After tests were complete at BC Children’s Hospital, Savanna was seen by a team from oncology. They explained to the family that although there was a chance something else was causing this mass, it was almost always a tumor. They did more x-rays and a CT Scan. On Thursday, January 16, 2020, they confirmed that it was cancer. The next testing stages were a little more invasive. Monday, January 20, 2020 Savanna had a surgical biopsy, and a CVC line was put into her chest so she wouldn’t need an IV in her arm. This would give doctors the access that they needed with as little intrusiveness as possible. She also had a bone marrow extraction.

Savanna has been diagnosed with stage 4 neuroblastoma. She is a little girl fighting the fight of her life at the tender age of 22 months. Her Mom and Dad are there fighting right alongside her, but to do that they are missing work, which, of course pays for everyday expenses, let alone extraordinary expenses. Any help that we could offer to their family right now would help to alleviate other burdens and allow them to focus on the health and life of their little girl.

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By Brokers Who Care May 9, 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 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.
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.
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