June 2017

All You Need to Know About Race Day – Sunday, June 25, 2017

By |June 13th, 2017|News, Scotiabank Charity Challenge|

SPECIAL REQUEST: We're asking all of our 5km runners to meet at the Cassie & Friends booth in Charity Village (see below for location) between 9:00-9:15am so that we can all head to the starting line together for a 9:30am start time. Let's show everyone that JA matters by standing together in our C&F team shirts. [...]

May 2017

Andrea’s Tips on Managing Medications, School and Opening Up…

By |May 23rd, 2017|Injection, News|

Teens Taking Charge: Andrea’s JIA After being diagnosed with Juvenile Arthritis at the age of two, Andrea’s childhood and teen years were much different than those of her peers. Her experiences with doctors’ visits and medications from such a young age forced her to mature faster and understand things her friends could not. In [...]

April 2017

Canakinumab Access

By |April 13th, 2017|Advocacy, News|

ACT NOW: SIGN OUR ONLINE PETITION AT CHANGE.ORG JIA affects approximately 24,000 infants to teens in BC and Canada, or 3 in every 1,000, making it one of the most common causes of chronic disability in children. Ten to 20 percent of children with JIA have Systemic Juvenile Idiopathic Arthritis (SJIA), a severe and [...]

Cassie & Friends makes $140,000 gift to ease the pain of children’s arthritis

By |April 10th, 2017|News, Past Research|

Donation marks ten years of dedicated support for kids and families affected by Juvenile Arthritis and other rheumatic diseases in British Columbia and Canada. Cassie and Friends is proud to announce today our $140,000 gift to BC Children’s Hospital to support children and families affected by Juvenile Arthritis – a painful, lifelong condition in [...]

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Teen shares PFS story and tips in new website

By |April 10th, 2017|News|

A teen has created a new website detailing what it's like to grow up with Periodic Fever Syndrome (PFS). When asked to design a "Personal Project" for a school assignment, the teen knew this was the perfect opportunity to spread more awareness about PFS and maybe even help other kids and families who are newly diagnosed or struggling [...]

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