March 2025

#KidsCantWait: Christina’s + Isabella’s Journeys

By |March 18th, 2025|#KidsCantWait, Blog, JIA, Ontario, Stories, Toronto|

#KidsCantWait: Christina's + Isabella's Journeys Hi, my name is Joscelyn Daskalopoulos, and this is our family’s story of living with Juvenile Idiopathic Arthritis (JIA) — a disease that affects two of our three children. Our journey began when our second child, Christina, was diagnosed at just one year old. She [...]

#KidsCantWait: Olivia’s Journey

By |March 18th, 2025|#KidsCantWait, Blog, JIA, Ontario, Stories, Toronto|

#KidsCantWait: Olivia's Journey Our daughter’s journey with Juvenile Idiopathic Arthritis (JIA) has been a difficult process but one that has taught us many things, including resilience and patience. Olivia was diagnosed at 15 months of age but started showing symptoms around 10 months. She first presented with symptoms of neck [...]

February 2025

From Patient to Pediatric Rheumatologist: Dr. Molly Dushnicky

By |February 10th, 2025|Advice, Blog, Hamilton, JIA, Ontario, Research, Stories, Work + Careers|

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 [...]

January 2025

Paige’s Journey with Juvenile Idiopathic Arthritis

By |January 6th, 2025|Advocacy, B.C., Blog, JIA, Stories, Vancouver|

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 [...]

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