PROUD TO SUPPORT TODD PACHAUER – 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 $2,000 to Todd Pachauer & Family, Recipient of the 1st Quarter vote of 2020.

Julie Anne Pachauer was born March 31,1977 and passed away April 24, 2019. She is survived by her husband Todd Pachauer and 3 young sons, Walton, Newton and Edison ( 7, 5 and 3).  Her unwavering grace & Todd’s amazing dedication to her helped them to cope with the terminal diagnosis that she received, which was ALS.

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

Nomination Story
Julie Anne Pachauer was born March 31,1977 and passed away April 24, 2019. She is survived by her husband Todd Pachauer and 3 young sons, Walton, Newton and Edison ( 7, 5 and 3). Julie was a talented artist who worked in the movie industry creating 3D props for films. Her name is in the credits for Cabin In The Woods (Horror movie) and many TV series. Her attention to detail was outstanding.

Her unwavering grace & Todd’s amazing dedication to her helped them to cope with the terminal diagnosis that she received, which was ALS. Todd had to close his successful jewelry store to stay at home and look after Julie as well as care of their 3 growing boys.

Todd’s parents have since moved into the family home to help out with the boys and to give Todd some relief.

Please see Julie’s  obituary.

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