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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PROUD TO SUPPORT Let's Cure Lucas RECIPIENT EASTERN 1st QUARTER 2026

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.

PROUD TO SUPPORT Lisse's Family Fighting for Healing and Stability RECIPIENT WESTERN 1st QUARTER 2026

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.

PROUD TO SUPPORT Andrea Mundie RECIPIENT 3rd QUARTER 2025

By Brokers Who Care • November 3, 2025

Brokers Who Care voted and we are pleased to announce that we will be sending a cheque in the amount of $10,000 to Andrea Mundie our Recipient of the 3rd Quarter 2025 vote. Thank you Marci Deanefor bringing this Cause to our attention. Andrea Mundie is a devoted mother of four—Rex, Dace, Clove, and Penn—facing the fight of her life. Already living with Stage 4 cancer, she has now been diagnosed with leptomeningeal disease, a rare and aggressive complication. Her priority is simple yet profound: to spend meaningful time with her children and create lasting memories while she can. To extend her time, Andrea has begun permanent chemotherapy. But the financial strain is overwhelming. Many of her most urgent needs are not covered by insurance. Funds raised will directly support: Health and wellness costs to ease her treatment Meals and home care for her children Educational expenses to secure their futures Despite her challenges, Andrea’s resilience shines. She celebrated her 50th birthday with loved ones, even while beginning chemotherapy. Soon after, she faced emergency surgery where her heart stopped and doctors cracked her ribs and sternum to save her life. Through it all, she has held onto positivity and humor. A grant from 100 Brokers Who Care would ease Andrea’s burden, giving her peace of mind and the ability to focus on what matters most—her children. Your support will provide comfort, dignity, and precious moments of love and memory.