I graduated from the University of British Columbia in 2022 with a Bachelor of Science in Biology, with a focus in Genetics and Evolution. Shortly after graduating and working in a laboratory, I came to the realization I can make a bigger impact in healthcare and biotechnology by leveraging my scientific expertise to [...]
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 [...]
Throughout my life I have been granted many titles; mom, wife, daughter, registered nurse, and writer are just a few. These are the titles that are associated with my name. I could be described as outgoing, humorous, modest, and perhaps kind too. These would be some characteristics that people from a distance would use [...]
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 [...]
"I soon began to experience extreme pain in my wrists, which would cause challenges for me whenever I would be at school or would work on school assignments." My name is Jessica Gill. I am from Toronto, Ontario, Canada. I was diagnosed with Juvenile Idiopathic Arthritis at the age of eight years [...]
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 [...]
"Throughout all of these experiences that I have had with Cassie + Friends, there is one throughline: Understanding. Understanding is a concept not to be underestimated." Meet Ciara. It was after after my body couldn’t row anymore, my hands couldn’t hold the pencil, my joints ached in pain, and after my diagnosis of [...]
Last summer, I was ready for an adventure. I wanted to trudge into unknown territory and immerse myself somewhere outside of my university town. Here's what I did to keep my arthritis in check, before, during and after my 18-day trip exploring France and Portugal with friends. Traveling with friends as a young [...]
"Hi, my name is Naina and I am 9 years old. This summer I was diagnosed with an autoimmune disease, Lupus. I hope to inspire kids like me to be brave and courageous. I want to spread the message that kids can get through anything with strength. Artwork has been a way for [...]
It is not easy being rare. Being rare means that there is not a lot of knowledge, research, and treatment options available for youth and families affected by systemic autoinflammatory diseases (SAIDs). And that is exactly what the recently formed Can-SAID advisory group, a branch of Cassie + Friends (C+F), wants to change. [...]
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