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Vancouver

#KidsCantWait: Ziyaad’s Journey

The First Signs Ziyaad was born on January 2, 2017, and he is now 8 years old. He has 2 older siblings, a sister, Nureen age 18, and a brother Fayaaz, age 16. He also has a cat, named Leo. Ziyaad enjoys being outdoors, swimming, biking and hiking. He is…

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Paige’s Journey with Juvenile Idiopathic Arthritis

To have a chronic illness is to be fighting every day for the next. My name is Paige Simpson. I am 17 years old, I was diagnosed with Juvenile Idiopathic Arthritis, otherwise known as JIA. I have been treated for JIA for 15 years but have been battling this condition…

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Youth Story: My experience with JIA and finding Cassie + Friends

“Throughout all of these experiences that I have had with Cassie + Friends, there is one throughline: Understanding. Understanding is a concept not to be underestimated.” Meet Ciara. It was after after my body couldn’t row anymore, my hands couldn’t hold the pencil, my joints ached in pain, and after…

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Highschool, Football, & Back Pain: Ryan’s Story

“Explaining this to fellow highschoolers was difficult, often times just resulting in being the butt of the joke. It was hard finding someone who understood and could relate.” Meet Ryan. I first started noticing symptoms as early as age 12. At that time, many just advised me that I was…

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“His friends have no idea what he has gone through.”

I don’t know if there can be a ‘typical’ journey for a young child who receives a Juvenile Arthritis diagnosis. But this is Linden’s story so far. When Linden got sick at 18 months old, we thought it was just a cold. But then came an unusual rash and his…

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Artist, Lacrosse Player, Friend, Big Sister – How I Learned to Love Who I Am

Hello, my name is Grace Parker Palidwor. I was diagnosed with juvenile idiopathic arthritis when I was 18 months old. In the first few years of my diagnosis, I don’t remember much except that I believed that every child was exactly like me. I believed that all my friends woke…

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Meet Sofia. She’s transforming lives in the JA community as a Cassie + Friends Youth Research Advisor.

A vital part of the work we do at Cassie + Friends stems from our involvement in important research in the pediatric rheumatic (PR) disease community. Over the past decade, we’ve helped endow a research chair, fund a new international post-doc, build one of only three PR labs in Canada, launch…

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Jaylene’s Story: SJIA

In September of 2014, summer ended and our three daughters headed to back school – Anika into grade 4, Jaylene to grade 3 and Claire starting preschool. With school routines starting up again, life seemed back to normal. Then, out of the blue, Jaylene began complaining about a rash she…

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