#KidsCantWait: Laila's Journey The Start of Our Journey Laila’s journey started when she was just six years old. She began complaining of leg pain, something that many parents might chalk up to growing pains. We thought, like most parents, that it was just a phase—something that would pass [...]
Blending Lived Experience with Research: Brittany's Story Hi! I’m Brittany – and I’m here to share with you a bit about my experience as someone who works in health research and lives with Ankylosing Spondylitis! I currently work as a Senior Research Associate at the University of [...]
#WhyIRun - Jana + Roam's Story Parenting a teen can be tricky. Parenting a teen with a painful rheumatic disease like Juvenile Idiopathic Arthritis can be heartbreaking. But it can also be incredibly inspiring, as you'll learn from Roam's mom, Jana. She was reminded of her son's strength and resilience during our Team Cassie [...]
My name is Maryse Hendi and I live in Calgary, AB. In 2012, at age 10, I was diagnosed with lupus. Lupus is a disease in which the immune system becomes hyperactive and attacks healthy tissue, joints, and organs in the body. On May 1st, I celebrated a milestone in my lupus journey: my [...]
There are lots of ways to show your support for the Juvenile Arthritis community on #GivingTuesday - like, share, educate and, of course, donate. To get inspired, we thought you might like to meet Jeremy from our Calgary CREW. On Nov 30th, we hope you'll join Jeremy and our CREW of parents/friends all across [...]
Road trip Alert! Starting Monday, April 29th, Cassie + Friends at School Puppet program will tour ten Calgary-area elementary schools to educate over 2500 students, parents and educators about Juvenile Arthritis and help affected kids at school. The tour is part of a huge push we are making to expand our Cassie and Friends' [...]
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