To recognize Juvenile Arthritis Awareness month, we're highlighting stories from the youth in our community: their diagnosis, their journeys, what they’ve learned, and most importantly, their advice. At Cassie + Friends, we believe that all kids deserve to live pain-free. In Canada, 24,000 children, teens and their families will be affected by Juvenile [...]
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COVID-19 Vaccination Study Children's Healthcare Canada and ScienceUpFirst, with funding from the Public Health Agency of Canada, have declared February 23, 2023, to be National Kids and Vaccines Day 2023. As such, we wanted to bring you an important update from our research partners, the [...]
To recognize rare disease day, we want to shine a light on all rare diseases, including the story of Zahra, whose rare autoinflammatory disease is still unknown, despite extensive genetic testing. Rare diseases affect 300 million people worldwide, and many of the 24,000 children in Canada in the pediatric rheumatic disease community are [...]
We would like to share a message from one of our Cassie + Friends families whose journey with Juvenile Arthritis has been made just a little bit easier, thanks to donors and friends like you. My 5 year old daughter, Eve and I are thankful for your constant support. Eve was diagnosed [...]
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. [...]
Our family's journey with Juvenile Idiopathic Arthritis (JIA) and genetics doesn’t begin with our son’s experience - it actually begins with mine. I was diagnosed with JIA at the age of 7; I faced a difficult time with poor control of my symptoms, which led to significant damage by the time I was [...]
Congratulations to Jake Shiell and Emma Linsley, recipients of the 2022 Cassie + Friends National Youth Leader Awards! Read Jake and Emma's full bios and project descriptions below. Interested in being considered for an award in 2023? To learn more about the Youth Leader [...]
"I was known as the 'girl who gets sick easily' within my family. This really impacted my mental health and acceptance for JIA for years." Did you know? Living with Juvenile Arthritis (JA)and other childhood rheumatic diseases like Lupus and JDM can increase your child's risk of depression [...]
All of these biologic changes are stressful and confusing! Over the past year, the landscape of biologic treatments available, and coverage for these treatments for children with JIA and other rheumatic diseases has changed. The biggest changes have been a shift to coverage of biosimilar treatments in many provinces, biologic shortages, and phasing out [...]
If you or a loved one is dealing with Juvenile Arthritis or any rheumatic disease, you're not alone. Sign up now for access to vital resources, news, and events. Join a supportive community that gets what you're facing. Together, we can make a difference in your Juvenile Arthritis journey.
Join us in creating a pain-free future for kids by becoming a monthly donor! Your support will give kids and families across Canada the care, education and resources they deserve. Click here to learn more!
