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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Meet Maia

On April 5th, 2017, our world came crashing down on us. Our 3-year old daughter Maia was diagnosed with Very High Risk Acute Lymphoblastic Leukemia. She hadn’t been herself for a few months, but there were no indicators that it was something so serious. A few weeks before her diagnosis, things changed.

She developed a fever that wouldn’t go away, had many bruises on her legs, no appetite, and little energy. The day we brought her to the Children’s ER, she had little blood spots on the bridge of her nose. Hours later, we were given the news that would change the course of our family’s life, and begin Maia’s fight for her own.  

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Meet Ella

Ella has STXBP1, but there is so much more to know about her. Ella is a lovely, happy, and loving 9 year old girl. She loves to make friends, and has a soft spot for babies and dogs. She can’t pass by anyone who is crying unless she stops to comfort them, especially a crying baby.

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