October 2022

A Pain-Free Future for Kids – One Step(pingstone) at a Time

By |October 18th, 2022|Blog, Hamilton, Movement, News, Research, Stories|

Three-year-old Katherine can keep up with other kids now, but that wasn't always the case... When Alana noticed her daughter was limping at the playground, she didn't know what to think - especially when the limp didn't go away. She decided to bring her to a doctor to be examined. After weeks of testing [...]

September 2022

When life gives you lemons…

By |September 9th, 2022|JIA, London, Medication, Ontario, sJIA, Stories|

Make lemonade! At least that’s what Jacob Shiell did when he was diagnosed with Systemic Idiopathic Juvenile Arthritis (SJIA) on his eighth birthday in October 2021.  Jacob’s journey began with unexplained foot pain and swelling. Over the next few weeks, the pain and swelling worsened and spread to his right knee, elbow and wrist. [...]

June 2022

Jenna’s Story – Enthesitis related arthritis

By |June 20th, 2022|Advice, Blog, JIA, Medication, Physical Activity, Stories|

We have been asking youth with rheumatic disease to share their story! Sharing stories helps build community and connections. We hope that Jenna’s amazing story inspires you to share your own story.  My name is Jenna Kedy. I am 18 years old and live in Halifax, Nova Scotia.  As a child, I was often [...]

May 2022

Read Why I’m a Team C+F Youth Ambassador

By |May 16th, 2022|About JIA, Advice, JIA, Physical Activity, Resources, School, Stories|

In early 2022 we launched the Team Cassie + Friends Youth Ambassador program to support youth in raising awareness of JA and other rheumatic diseases within their school community. Soleil is one of our first Team C+F Youth Ambassadors! This month she will give a presentation to her entire school on Juvenile Arthritis and [...]

March 2022

Meet Addie!

By |March 22nd, 2022|JIA, Northern BC|

Addie, Prince George, BC 14 years old, Psoriatic JIA I used to hike and play school sports like basketball and volleyball. Now, I’m not able to because my arthritis hurts too much in my elbow, ankles and knees. This last year I started on the volleyball team, but had to stop playing because of [...]

Q+A with Carrie Ritchie, C + F Board Member, on her daughter’s recent JIA diagnosis. 

By |March 11th, 2022|About JIA, JIA, Stories|

Meet Carrie Ritchie! Carrie is a member of the Cassie + Friends National Board of Directors and a parent of a child with Juvenile Idiopathic Arthritis. We caught up with Carrie to learn about her family's journey with juvenile arthritis over the last 2 years. As a board member, Carrie looks forward to helping [...]

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