about us

Cassie + Friends is the only charity in Canada dedicated 100% to the pediatric rheumatic disease community. Rooted in our four pillars, we champion research, education, connection and support for pediatric rheumatic diseases.

Working with patients, caregivers, healthcare professionals, researchers, and other friends, we’ve created a life-changing community to help kids and families face the ups and downs of life with a chronic condition – so that no child has to live in pain alone.

We’ve shown what’s possible, but there’s lots more to do.

our story

Despite being the most common cause of chronic disability in children, affecting 24,000 kids across Canada, Juvenile Arthritis remains relatively unknown and drastically under-resourced. This is our history…

The story of Cassie + Friends, Take a Pain Check Podcast

Hear from Cassie + Friends Co- Founder and Board Chair, David Porte, as he shares how Cassie + Friends began on the Take a Pain Check Podcast!

our impact

$1,000,000+

Dollars invested in new research into safer, more effective treatments for kids

We fund initiatives that quickly use the results of research to give new hope and resources to kids and families living with rheumatic diseases. Our research partners include BC Children’s Hospital, the University of British Columbia, the Michael Smith Foundation for Health Research and SickKids Hospital.

$75,000

Direct annual support to kids and families

From financial support and equipment to connection and educational events, we make sure no child or family feels alone in their journey with rheumatic disease.

17,500

# of kids and teachers educated about JIA in BC schools

Our School Toolkit helps kids with arthritis gain more acceptance and inclusion at school.

34

# of parents trained to provide mentorship and support to others (and growing!)

Our Parent-to-Parent Support Program at BC Children’s Hospital matches experienced caregivers with parents in the first stages of diagnosis or during challenging times.

major challenges, big goals

Despite being the most common cause of chronic disability in children, affecting 24,000 kids across Canada, Juvenile Arthritis remains relatively unknown and drastically under-resourced.

  • A 2010 Ipsos-Reid poll confirmed that only 19% of Canadians are aware that arthritis can strike children.
  • There are only 35 to 50 practicing pediatric rheumatologists in Canada, largely based out of major children’s hospitals.
  • The indirect costs of a child’s rheumatic disease can be enormous. Affected children can lose several weeks of school each year, while parents deal with salary loss, missed work and frequent travel to care for their children. A Nova Scotia study found that most parents paid ~$700/year for out-of-pocket expenses, with huge variability of patient/family needs ranging up to 37% of annual household income.
  • Access to early diagnosis, affordable care and timely treatments are urgent issues affecting kids and families.
  • A 2016 study found that one in seven out of a population of 102 adolescents with JIA were found to have significant symptoms of depression.
DONATE NOW

join us

Attend an event, connect with others or stay up-to-date on our latest news and research.