Stories
Every young person’s journey with rheumatic disease is different. These stories share the lived experiences of youth who are navigating challenges, building confidence, and finding their voice.
Through connection, support, and community, these young people are showing what’s possible — and helping others feel less alone along the way.
#KidsCantWait: Harley’s Journey
Harley is our tiny warrior. Just after turning 2, in August 2022, Harley started having difficulty walking one day out of nowhere. It pained her to tears and she had to hold onto someone to walk or be carried. She was on Amoxicillin for an ear infection, and had also…
Where Are They Now: Zahra’s Story
In this special Rare Disease Month edition of “Where Are They Now”, we caught up with Zahra Alidina. In 2023, Zahra shared what life was like living with an autoinflammatory disease that is so rare it doesn’t even have a name. We’re so honoured to share this update from Zahra below.…
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 Calgary, where I’ve had the opportunity to work on projects…
From Patient to Pediatric Rheumatologist: Dr. Molly Dushnicky
Dr. Molly Dushnicky’s story sounds like a lot of her patients’: When she was just 18 months old, she stopped walking, her knees wouldn’t bend easily, and she wasn’t her usual happy self. That’s when she was diagnosed with Juvenile Idiopathic Arthritis (JIA). Now, Dr. Dushnicky is a Pediatric Rheumatologist…
Raising Awareness, Sharing Hope: One Family’s Journey with SJIA
We’re so excited to introduce Tamara Schnarr, one of our new parent ambassadors for the Kitchener-Waterloo region! Tamara, a Realtor with a background in marketing, graphic design, and event management, is passionate about giving back to her community and is looking forward to supporting Cassie + Friends’ mission – a…
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…
Attacking Barriers: Fencing with JIA
For a lot of kids, being diagnosed with a rheumatic disease, like Juvenile Arthritis (JIA), means adapting to a whole new way of life. Today, we’re honoured to share the story of Paula and her son Simon, who was diagnosed with Enthesitis-Related Arthritis (ERA) two months ago. While navigating this…
Navigating Medical School: Alejandra’s First Year
Our Youth Mentor, Alejandra, reflects on her experience in medical school and shares what it’s been like as she navigates her first year. Many youth with chronic illnesses, like JIA, often aspire to be doctors or other healthcare providers, as they are inspired by their own lived experiences to help others. Thinking…
Alison Legge: Navigating the Workplace with a Rheumatic Disease, Part 2
Earlier this year, we heard from Alison, who shared her story about navigating the workplace with a rheumatic disease. Now in her new role, Alison shared an update with us about her journey, and how what she has been through over the last few months has shown her that she made…
Building Community and Mental Health Support for Students with Rheumatic Diseases: Ciara’s Story
Living with a chronic condition like a rheumatic disease can be especially challenging for young people, not only physically but also mentally. It’s no surprise that 40% of youth diagnosed with a rheumatic disease experience symptoms of anxiety, depression, or panic disorders. However, a strong support system and connection with others…
#WhyIRun – Audrey’s Story
In this #WhyIRun, we hear from the Rose family, who share their daughter Audrey’s journey with Juvenile Idiopathic Arthritis (JIA). Audrey and her family will be participating in our upcoming run/walk at Hamilton’s Road2Hope marathon on November 2, 2024, where they are not only the top fundraiser for Cassie +…
True North Resilience: Kira Young’s Story
At Cassie + Friends, we believe that every child and family should have access to timely and optimal rheumatic disease care. That’s why we launched the C+F Northern BC Project, to better understand the barriers to diagnosis, care, and patient support for families living in remote/rural communities and explore how we…