Meet Azariah

Azariah was only three months old when her family learned that she had a rare form of kidney cancer called Wilm’s Tumour. It was rare enough for someone as young as Azariah to be diagnosed, but even rarer to have tumours on both kidneys.

Over the last three years, Azariah has been an absolute trooper, handling all of the tests and treatments along the way. It has been so incredibly tough on her parents and her siblings, and this whole family could benefit from some of the hope and joy that comes from a dream come true.

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Meet Karmyn

What started out as a few random fevers throughout the summer of 2018, turned into an emergency room visit and news that turned our whole world upside down. During the early hours of August 25, 2018, we found out that our little 6-year-old Karmyn had cancer.

A few days later, she was formally diagnosed with Acute Lymphoblastic Leukemia. Two weeks after that, it was concluded that Karmyn had Philadelphia Positive ALL, which is very rare in pediatric Leukemia in that less than 5% of kids have it. Since then, Karmyn has turned 7 and her days have been mainly filled with trips to clinic at CancerCare, and admissions at Children's Hospital on CK5.

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Deadlifts For Dreams

Elevator doors opened up to reveal Maya, who had just finished a round of chemo, singing Lion King songs at the top of her lungs, delighting the other patients and parents in the Children’s Hospital cancer ward.

“She loves Lion King,” Maya’s mother, Sarah says, laughing. “But she doesn’t really know the words, so she just sings what it sounds like to her.”

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Meet Maya

Maya is a strong, determined little girl who hasn’t let cancer stop her from doing the things she loves, like playing with her big sister Brielle, singing and dancing. She LOVES singing along to Barbie movies with her sister. She is a little girl with a BIG attitude and knows exactly what she wants.

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Meet Colten

My name is Darrell Poirier. On November 14th, 2014 my wife Melissa and I, along with our son Liam were very excited to welcome our newest addition to our family, Colten. Or as we call him, Coco.

Colten came to us without any complications, but as Melissa was snuggling her beautiful new baby, she noticed a small scab on the back of his head. Little did we know, this would be the start of his battle with the ever so stubborn and rare Langerhans Cell Histiocytosis (LCH). At 4 weeks, another scab appeared on his neck. Then, by 8 weeks old, his torso was covered front to back.

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WPG CYCLE: Spinning For A Dream!

This January, local entrepreneurs and owners of WPG Cycle Christy Weiss and Jamie Murray decided that they wanted to make a difference. They were going to make a dream come true. 

Christy and Jamie strive every day to build a community that is safe, inclusive, and positive. It was nothing short of destiny when they learned that there was a little girl out there dreaming of finding exactly that: community

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