On May 25, 2018, Vancouver Skating Club (VSC) and Bantam Female North Shore Avalanche Hockey teamed up for a donate-to-skate event in support of Team Cassie and Friends. With over fifty people in attendance, the event, organized by long-time C+F community members Lorna and Naomi Bauer, raised over $600 for kids and families affected by [...]
I want to let you know why I am walking this Charity Challenge for Cassie and Friends. “Autoimmunity is the system of immune responses of an organism against its own healthy cells and tissues. Any disease that results from such an aberrant immune response is termed an 'autoimmune disease.'" My dad’s cousin Gladys Marie [...]
Team Cassie and Friends will be participating in the Scotiabank Charity Challenge Run/Walk on June 24th. Wondering what this day is all about? Here are some frequently asked questions to put your mind at ease and help you get registered before race fees go up on May 18th! What happens on race day? Race day is full of excitement! Meet at our charity booth [...]
On Thursday, April 19th, the members of the Cassie and Friends Society Board, youth leaders and parent volunteers came together for our Annual General Meeting. We are excited to share the report provided by Cassie and Friends' Co-Founder and Board Chair, David Porte, outlining the amazing things we've been able to achieve this past [...]
Each year students at St. Pius X (SPX) Elementary School in North Vancouver put their talents on display at their annual variety show to raise funds for a local charity. This year, thanks to SPX alum and C+F volunteer Alison Legge, those funds will go to help kids and families affected by Juvenile Arthritis [...]
We are excited to share this amazing coverage in the March 23rd issue of the Jewish Independent newspaper on our work to spread Juvenile Arthritis (JA) awareness in schools. The article highlighted our Kids on the Block (KOB) puppet show program, which has now been seen by well over 25,000 kids and educators all over [...]
Cassie and Friends Society, in partnership with Arthritis Consumer Experts, is leading a call for the BC Government to drastically improve the outlook of children with SJIA by allowing reimbursement coverage for canakinumab for the small number of children who need it. Our campaign for equitable access has now reached the media, Premier John Horgan and Minister [...]
Our annual Family Day conference for Juvenile Arthritis and other rheumatic diseases is just around the corner - and we can't wait! On Saturday, September 16th, we'll welcome over 80 families and 350 attendees to enjoy a day of connection, learning and fun! Interested to know what's in store? Check out our Conference Program below! [...]
One of the hardest and most nerve-wracking decisions for children and teens with juvenile arthritis (also called juvenile idiopathic arthritis) and their parents is deciding when to stop medicines. The doctors from Pediatric Rheumatology at the BC Children’s Hospital in Vancouver, BC, Canada are working with other researchers based at Rutgers University (NJ) and from [...]
I was diagnosed with Juvenile Dermatomyositis (JDM) in December of 2014. So, to help you understand; Derma, is skin and myo is muscle and sitis is inflammation. I have to take injections of Methotrexate once a week and when I was first being treated I had to take prednisone for 4 months. It is not [...]
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