PROUD TO SUPPORT – THE RUEL FAMILY RECIPIENT FOR 1ST QUARTER 2021

100Brokers • March 5, 2021

On behalf of The Ruel Family, THANK YOU for your generosity!!

100Brokers Members voted and we are very pleased to announce that we will be sending a cheque in the amount of $4,050 to The Ruel Family, Recipient of the 1st Quarter vote of 2021.

Thank you to Jodi Whalen for bringing this Cause to our attention.

Nomination Story

On December 30, 2020 Neil and Kristen received the news that no parents want to hear, their baby girl Callie has an inoperable brain stem tumor that has been diagnosed as a Diffuse Intrinsic Potine Gliomas (DIPG) tumor, which is terminal. This form of cancer is very rare, with only 3 other cases diagnosed in Canada in 2020. Callie is the light of their life, so this news is completely unfathomable.

Neil, Kristen and their 3 daughters Zophia, Lilah and Izzy need support so they can all be remain together as a family to support Callie as they navigate future challenges in her journey. The family will require financial assistance to replace lost income, provide immediate financial relief, future medical support for Callie, and counselling support for the family.

A post from her dad really had me tear up reading this.

Another day has come and gone. Sweet Callie had dark bags under her eyes but they still glimmer and shine. She looks up to her “mama” and says with a smile “I tired” followed by her fake but oh so real yawn…

Mom picks Callie up and starts walking her up to bed. I tell her I love her so much and give her a kiss on the forehead. Sometimes she tells me she loves me, sometimes she doesn’t but I know she does. Mom takes her upstairs and calls down to me. “Babe can you bring up her…” tablet, soos or both. I happily run it up and get one more look at my baby girl, give her the item and she always responds “Thank you my dad.” There is and was no better feeling. Mom and I watch through the monitor as little Callie rolls on her side and watches her tablet until she slowly closes her eyes and falls asleep.

Then reality strikes, is this the last time? Will she wake up? How are we all going to survive this loss, the pain, the emptiness that will never go away.

Mom and I look at each other and with a quiet nod we both know what the other is thinking and we start to watch a show or play on our phones to lose ourselves for a brief moment before we tuck the other children in for the night and have to go to bed. The one place neither of us wants to endure because that awful reality awaits us. Hopefully one more day is the phrase that constantly wonders through my mind.

It’s bedtime but I cannot sleep. I lay there aimlessly for hours reading random articles on my phone, checking Facebook, playing games and watching the monitor to make sure Callie is still breathing. Mom slowly falls asleep first as she is utterly exhausted from being awoken numerous times the previous night before finally being up for the day any time between 3:30 and 4:30 in the morning. I continue to lay restlessly and make sure my alarm is set for 6:00am because Mom and I have made it known that if Callie does not wake us up in the morning and suddenly passes away in the night, I chose the responsibility of finding her in the morning. It’s the least I can do for Mom as we both know she would never come back from it.

For the next few hours I contemplate the family’s future. I try to distract myself with copious amounts of planning but it all comes back to how do it fix this? Deep down I know I can’t but it is who I am and not something I can just turn off at a moments notice.

Every night it is the same, funeral, memorial, therapy, counselling, finances, another new normal at home, going back to work, and not just surviving through this myself but being the pillar my family needs to survive this pain. I think we all understand that this will always be a part of us and it isn’t something we will just “get over” in time but what can I do for everyone to move on?

I know it’s not fair but I still cannot wrap my head around knowing that there is a finite amount of time with Callie. It hurts to see her struggle, it hurts to watch her slowly regress and it kills me to know that sooner than later she will not be with me anymore.

That’s when it hits me the hardest. It happens when it’s quiet, it’s dark, everyone is asleep and I am alone with my thoughts. I tear up from this overwhelming guilt that it is her and not me, I tear up from joy remembering all of her cute little sayings and quirks and I tear up from sadness because I am going to miss her so much.

The fatigue from this different type of stress wears me out and places a heavy weight on my eyes. As strong as I think I am, I cannot fight falling asleep forever. I hope and pray it isn’t the last night but eventually concede that I cannot control this fate. Slowly I fall asleep hoping my alarm doesn’t wake me up first, hoping I hear a giggle, a scream, a cry, anything from Callie because then I get one more day. How long will this groundhog’s day continue? Every night I ask for one more day.

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.
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.
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