stories

For this edition of, “Where Are They Now?”, we caught up with Ravia Frison. You may remember Ravia from our What is JIA video, where she poignantly shares what it is like to live with an often invisible disease like JIA. We’re so honoured to share an update from Ravia, including some…

nternational Youth Day Edition: Tyler Mah + Gauri Raj For International Youth Day 2024, we’re delighted to announce a new series called “Where Are They Now?” At Cassie + Friends, youth are at the heart of everything we do, and we love being able to support them as they continue…

#ConnectingJA transforms Misinformation. “Cassie + Friends has been such a great resource for my husband and I, our son, and even Lily to understand the disease more.” Parent of a child with JA, SK #ConnectingJA transforms Opportunities. “While I have completed the Future Leaders Program, these new skills will continue to serve…

For those of us who live each day affected by juvenile arthritis or another rheumatic disease, it can often feel like there is no one who can understand what we are going through. Although this can feel isolating, when we share our juvenile arthritis and other rheumatic disease stories with…