My name is Kayla, I am 25 years old and have lived with arthritis for over half my life. I attended Pain Education Day at the International Symposium for Pediatric Pain last month, and it was not what I initially expected. I didn't realize I would have the opportunity to meet so many other [...]
When I first heard of the medication Ondansetron, I couldn’t help but think about how its name sounded like a character from the Transformers movies. While this medication doesn’t fight space aliens or have a special effects budget, it does hold the capacity to TRANSFORM lives. How might you ask?Methotrexate is a [...]
Inspired by the Roald Dahl Charity’s Marvellous Nurse Inventing Rooms, on August 23rd, we hosted our very own C+F Inventing Room to ask the community and together envision what our C+F Injection Coping Kits should include. With the help of medical experts, parents and youth, we dove in and got to work! We started [...]
Hi! My name is Hayley. I was diagnosed with JIA at the age of 13. Around age 12 I realized that I could not straighten my fingers. Young me was very medically inclined, so after some googling, I diagnosed myself with arthritis. It took a long time to convince the adults in my life [...]
Hello there! My name is Emily Bessey. I am 19 years old and live in Cole Harbour, Nova Scotia. My journey with JIA and TMJ started way back in 2009 when I was just 6 years old. I would go to school limping, hardly able to walk, but return home at the end of [...]
Hello, My name is Emma Linsley, and I am from Saskatoon, Saskatchewan. When I was 15 years old, I was diagnosed with JIA. Along with needing to learn to manage the physical ailments of the disease, this diagnosis brought with it a complex set of other challenges that my support network and I would [...]
6.5 million people are affected by arthritis in Canada and about 24,000 of them are children. Cassie + Friends is just for them. Kids like Audrey (pictured right) - diagnosed at just 18 months - need our help to make sure their health and futures are a priority, even beyond the dedicated care from [...]
I am the proud mother to a vibrant 3.5-year-old, Émilie, who was diagnosed with Juvenile Idiopathic Arthritis (JIA) shortly before her second birthday. We were fortunate as a family to receive a diagnosis in a relatively rapid timeframe thanks to knowledge about navigating the health care system (I work as a nurse) and a [...]
Meet Amy and Abby Mazzone - a mom and daughter duo who’ve been fighting JIA together, along with their family, for 12 years. As with many in our community, Methotrexate has played an important, yet, challenging role in their journey to find relief from pain and allow Abby to be a kid. Below, you [...]
Dear Friends + Partners, As part of our advocacy for Juvenile Arthritis Awareness Month, I am pleased to let you know about a special editorial by Cassie + Friends appearing today in the Toronto Star newspaper and digitally on healthinsight.ca. Click here for a link to the full article. Your voice is so important [...]
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