
NEWS
#KidsCantWait: Rylee’s Journey
The First Signs November 30th, 2016, Rylee Lynn Rideout arrived making us parents for the first time and becoming the first grandchild and niece in our families. The years that followed were nothing short of amazing, Rylee developed a love for life and a sparkle that we quickly knew would…
#KidsCantWait: Simon’s Journey
The Early Signs Simon’s journey began when he was around 10; he has always been an active, strong-willed child. He never complained when falling or having some scratches for his rough, playful adventures, but he wasn’t happy with our long walks. As a family, we love hiking, which seemed to…
#KidsCantWait: Rosalie’s Journey
As a parent/caregiver, you envision your children growing up happy and healthy, enjoying life to the fullest. However, life tends to chuckle at our best laid plans, and that was the case with our middle daughter, Rosalie, who was diagnosed with Polyarticular Juvenile Idiopathic Arthritis at the age of 6…
#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…
#VirtuallyAnything
Are you ready to take action for kids living with Juvenile Arthritis (JA) and other rheumatic diseases? Make an immediate impact on childhood rheumatic diseases by doing #VirtuallyAnything to help raise awareness, fund research, and support families. The problem: Awareness of rheumatic conditions in youth is extremely low—only about 20% of Canadians are…
Transforming Mental Health for Youth With Rheumatic Diseases
A recent report by Mental Health Research Canada underscores the pressing need for improved access to mental health services for youth. Vulnerable groups, including those already managing chronic conditions, face particularly steep challenges. Among these, youth with Juvenile Idiopathic Arthritis (JIA) and other rheumatic diseases experience disproportionately high rates of anxiety, depression,…
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…
A Year of Advocacy and Impact: Our 2024 Highlights
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…