PROUD TO SUPPORT PRESLEY JANE MECHAM WESTERN RECIPIENT 1ST QUARTER 2023

Brokers Who Care • Mar 17, 2023

Brokers Who Care voted and we are pleased to announce that we will be sending a cheque in the amount of $10,000 to Presley Jane Mecham and family, our Western Recipient of the 1st Quarter 2023 vote.


Thank you to McKay Wood for bringing this Cause to our attention.


The Nomination Story:

Presley was a normal one and a half year old. Cheerful, active, and busy, she was all go and no stop. The month of August 2022, however, proved difficult for her to function normally. After various trips to the ER on Aug 27th an unlikely nightmare, Presley had cancer and was diagnosed with Acute Lymphocytic Leukemia, an extremely aggressive form of cancer that can overrun one’s bone marrow, blood, and central nervous system in a matter of a few short weeks. The pain and trauma that Presely has endured over the past 6 months has been monumental. 

She and her mother were flown to Vancouver within a matter of hours, joined the next day by Father Daylon, and her older sister Nova. Due to her weakened bones and muscles, Presley didn’t walk for the next few months, losing all of her hair and has spent much of the time in a hospital room, most of it sitting or lying on a bed.


She recently turned 2 years old (Happy Birthday) and has been progressing through her treatments like a champion. The chemo treatments however have degraded her immune system and she has had several extra visits to the ER just to help fight infections. A small bug can mean 10 straight days in the hospital. Once, she developed a colon infection and was not allowed to eat for several days. All nutrients had to come through the IV. When she first arrived at the hospital she had two different surgeries just to insert a port-a-cath that would work. The first port became infected and had to be removed. They later inserted a new on the other side of her chest. She now bears matching scars on either side. 


In December, the treatments caused her adrenal glands to not function properly and she became hypoglycemic. Finger pokes every four hours and force fed juice or syrup when blood sugar got too low. Due to forced fasting and nausea from treatments Presley lost her appetite
as well. In order to get enough calories through the day she has been given a NG tube. A tube shoved up the nose and down into the stomach. She despises this more than treatments, needles, or ER visits. The tube has to be flushed throughout the day to keep it flowing. The
water stiffens the tube in her nose and causes an uncomfortable sensation as water she didn’t
drink hits her stomach. 


Presley has a long way to go over the next few years but she is brave and determined and showing progress. She is now able to walk again which is a huge step forward. There will still be a lot of ups and downs but she’s happiest with both her parents and her sister by her side. It has been a big adjustment for the whole family to be present and 100’s of kms away from home (Vanderhoof). 


In September, just weeks after her diagnosis the family moved into a newly purchased home that Presley has never been to and has been sitting empty for months. Mom has been the primary caregiver during this time and Dad is sole provider for the family. He has struggled to work remotely from Vancouver for the first several months. He has applied for a leave of absence but was not granted this and so last resort to try to qualify for compassionate care leave which is dependent on Employment insurance which is 55% of insurable earnings capped at $650 a week. Costs of a new home, travel, and prescription drugs have been staggering and the family is not sure what they are going to do to pay for the mortgage and support Presley in Vancouver. Ronald Mcdonald house has graciously provided accommodations in Vancouver but having used up most of their savings and with limited family support they are struggling to know the future, bracing for the worst and wondering if keeping their home with their new mortgage is what they should do. They are however committed to uplift and support their powerful 2 year old Presley who is the light and life of their world. 


By Brokers Who Care 12 Feb, 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 Shelly Thorpe and her daughter Heather, our Eastern Recipient of the 1st Quarter 2024 vote. Thank you to Monica Chrysler for bringing this Cause to our attention. The Nomination Story: Shelley experienced a tramatic birth of her daughter 26 years ago. Her daughter Heather had fetal distress and was without oxygen for several minutes leaving her with permanent brain damage. Heather has never walked, has never been able to sit up, or even feed heself. She is 100% at the mercy and dependent of others to care for her. She is aware of her surroundings, but trapped inside her body, trying to fit into society. Shelley has done everything a Mother could possibly give over the years, but her small home did not have the capacity to offer the care that Heather needed. When Heather turned 18, she went into a home care facility. Shortly afterwards the world turned upside down from the pandamic and Heather fell into a deep depression without having any visitors or even being able to get out for the day. Heather's immediate community worker has recently resigned, and she has been given an eviction notice from the facility as she is behind on her lodging and medical bills. Since Heather is in a special customized wheelchair, the only way she can travel is in a wheelchair assessible van, which they don't have funds for. Shelley and her daughter are extremely distraught because she is completely disabled and will soon have no where to live, unless they can catch up on these bills. Elevator pitch: Heather is unable to speak, walk, or take care of herself, but her spirit just loves to interact with others, or even hold the hand of a stranger. Heather and her Mom have been through so much, and now their difficult financial situation has landed an eviction notice from the lodging care facility she has been at for the past 4 years. Heather's brain damage at birth has left her at the mercy and care of others her entire life. The funds would help her to keep a roof over her head, continue with her care, and even help her to find a way to take a day trip out of the facility for even 1 day to the mall or beach this summer. She is trapped inside her own body, and her Mom has done everything a human can do to provide, but they need help....and I'm hoping and praying Brokers Who Care is the answer to their prayers....
By Brokers Who Care 12 Feb, 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 The Nicholls Family, our Western Recipient of the 1st Quarter 2024 vote.  Thank you McKay Wood for bringing this Cause to our attention. Their Story: We were a happy and healthy family of four living in Lake Country. My husband Matt had started his own company in security system technology, I was a busy Mortgage Specialist and our two young children were going to preschool together. In July 2021 things took a turn once we noticed that our almost three year old daughter Rylie had developed a limp. This limp progressed and one day she wouldn’t put weight on her legs at all. After trips to two different emergency rooms, we were admitted to run further tests. Within a day and a half, we were being transported down to B.C. Children’s Hospital with an MRI showing significant disease in her skeleton. We found out on our seventh wedding anniversary, that our little girl, just shy of her 3rd birthday was diagnosed with Stage 4 aggressive Neuroblastoma. Our world stopped. Everything changed in that moment. Statistics showed that she only had a 50% chance of survival, and if she made it, would then have a 60% chance of relapse with minimal chance of survival. I had to advise my employer that I could no longer work as I had to care for my daughter full time. Our family decided to divide and conquer - my husband and my 4 year old autistic son at home, and Rylie and myself fighting for her life in Vancouver. She went through 18 months of intense, traumatic treatments for her cancer. This included 6 rounds of induction chemo, 12 rounds of radiation, multiple surgeries, two rounds of high dose chemotherapy with autologous stem cell transplants, a trip to Sick Kids Hospital in Toronto for a month for high dose radiation contrast therapy, 6 months of immunotherapy and more. During her treatment we almost lost her a couple of times due to the treatment. But in January 2023 she rang the bell for being done treatment and cancer free. There wasn’t much joy however with the news as she had developed serious side effects during the treatment. Not only had she lost significant hearing, she wasn’t able to gain weight and had failure to thrive. The biggest concern however were her lungs. In November of 2022 she also lost her best friend Savanna, her twin flame who lost her life to the same cancer, Neuroblastoma. In 2023 even though she was done treatment, we were airlifted to Vancouver 5 times for lung related illnesses. We were able to go on her Make a Wish vacation in April before everything went downhill. In May, my children lost their grandmother, and I lost my mom. From cancer as well. She was only 66. The day after my mother’s funeral, Rylie and I were back in Vancouver for a lung biopsy to try to figure out what was going on. This procedure landed her in the PICU on life support and we were prepared that it may take her. But she pulled through. While we were in Vancouver recovering, my children’s other grandparents - my in-laws, lost their home in the Kelowna fires. This was devastating as their home was a safe place for my children. After Rylie’s stint in the PICU, we were able to make some more memories fortunately due to her resilience. We were able to go to cancer camp as a family, and celebrated her 5th birthday. She was also able to attend a few days of school in September. But by October, she was struggling more. And we were once again airlifted to Vancouver. Once she was strong enough she had a sedated CT, where we found out her lungs were in end stage failure. We made it to Canuck Place Hospice for some respite - but she knew it was her time. I told her Savanna and grandma were waiting and she took her last breath. Rylie’s life was remarkable. She is the poster child of B.C. Children’s hospital as her image is on buses, signs and all over social media. She battled every obstacle of her short life with grace. She is now at peace with no more treatments or hospital visits, but the rest of us will need a lifetime to recover. Rylie’s older brother Cameron by only 16 months has experienced more grief and loss these last couple years than any child should. And because of his grief he hasn’t been able to go back to school. He is needing counselling and therapies for his trauma. Matt’s still running his company but I haven’t been able to return back to work from being Rylie’s full time caregiver to her brother Cameron’s full time caregiver. We have experienced so much trauma and grief over the last couple years. But I do hope to use the heartache and grief and turn it into a life of advocacy, anwareness and philanthropy. I want to thank you all so much for taking my family into consideration.
By Brokers Who Care 21 Dec, 2023
Brokers Who Care voted and we are pleased to announce that we will be sending a cheque in the amount of $10,000 to Michael Hallett, our Western Recipient of the 4th Quarter 2023 vote. Thank you to Dustan Woodhouse for bringing this Cause to our attention. The Nomination Story: Many of you know this name, because Michael is an active Broker who shows up for our community on the regular, just last month volunteering to be grilled one-on-one at a CMBABC event. This could be written as a heartbreaking submission… This could be written as a rallying cry, rah-rah, submission… But none of our hearts need any more breaking, and I can confirm that Michaels spirit is not breaking. Nor are the spirits of his wife & their 16yr old son. An accident on Aug 31 put Michael on his back, and in the hospital, where he remains for some time to come. Limited movement, a ventilator, and a long road ahead are the current reality. But, he’s alert, and he’s all there from the shoulders up, although communication is limited by our (variable) lip reading skills due to the ventilator. This experience is coming at the Hallet family hard & fast, with many unexpected costs, the physical, the emotional and of course the financial. As prepared as each of us thinks we are for whatever life throws our way, sometimes we could still use a hand. Family and friends have rallied, levels of support for Michael, and for one another, have been amazing – more than anyone would expect. A testament to how much Michael has given to those around him throughout his 47 years. And while the path forward isn't yet entirely clear, one thing is – his new path will be an expensive one. Michael has been an amazing face for the Brokering industry, he has made us all look good. Now is the time to say thank you in this wonderfully meaningful way. Please rally for Michael & his family.
Show More
Share by: