From Fear to Confidence: Because Kids Can’t Wait Every day, kids and families living with Juvenile Arthritis and other childhood rheumatic diseases carry fear, uncertainty, and the challenges of lifelong illness. Your gift helps them reach a turning point — toward clarity, readiness, and confidence. Donate today Why Confidence? At [...]
Life with PFAPA: Kai’s Journey from Diagnosis to Now We’re honoured to share a guest blog from one of our incredible youth in the community, Kai. Diagnosed with PFAPA at just seven years old, Kai faced more than most kids his age. Read more about Kai and his journey below. Looking to [...]
#WhyIRun: Emma's Hope My name is Emma Linsley, and I was diagnosed with Juvenile Arthritis eight years ago, when I was 16. At last year's Saskatoon run, I had a deeply moving conversation with the mom of an adorable boy who has JA. We talked about the challenges of living with JA, and [...]
TOP FIVE TIPS FOR BACK TO SCHOOL SUCCESS WITH JUVENILE ARTHRITIS Back-to-school can be exciting—but for families and youth living with juvenile arthritis (JA) and other rheumatic diseases, it can also feel overwhelming. Between medical care, school prep, and new routines, there’s a lot to juggle. At Cassie + Friends, we’re [...]
Navigating Morphea – Michelle’s Story For most of my life, I’ve had Morphea. Starting as a red mark on my chin as a young child, it eventually turned darker and over the years, spread to areas on my forehead, and neck. Morphea, also known as localized Scleroderma, is [...]
Living with JIA – Lisa’s Journey It started out as sharp pain in my hips which I believed to be a pulled muscle; however, it soon progressed into a severe pain and stiffness. Days passed as I used crutches to simply walk around, and I remember that any [...]
#WhyIRun: Chase's Story Meet Chase, a brave and resilient 4-year-old from London, ON, who is inspiring his family, friends, and community to step up for kids affected by Juvenile Dermatomyositis (JDM)—a rare autoimmune disease that causes muscle weakness and skin rashes. This year, Chase’s family is joining Team Cassie + Friends to [...]
Growing up with JDM - Layla’s experience My experience with the healthcare system started earlier than most. I was diagnosed with Juvenile Dermatomyositis (JDM), a rare autoimmune disease that affects the muscles and skin, and since then, the Montreal Children’s Hospital has been a constant part of my life, [...]
Still Shining: Ava’s Journey with Juvenile Ankylosing Spondylitis May is Ankylosing Spondylitis (AS) Awareness Month. Many people think of AS as a condition that affects adults, but it can begin in childhood, too. Ava’s story is a powerful reminder of the resilience of kids living with Juvenile Ankylosing Spondylitis and the importance of [...]
#WhyIRun: Stephanie + Tommy's Story Meet Stephanie, who is running with Team Cassie + Friends to raise awareness for Juvenile Arthritis for her son, Tommy! Diagnosed with oligoarticular Juvenile Idiopathic Arthritis (JIA) just after his second birthday, Tommy’s journey has been full of ups and downs. Read more about their story below, and [...]
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