Hi Everyone! My name is Ciara, and I am working as an Administrative Assistant at Cassie + Friends this summer I am 19 years old and have just finished my first year at the University of Toronto studying English Literature. One of my favourite forms of Literature is Epic poetry (ex: The Odyssey). I am [...]
In early 2022 we launched the Team Cassie + Friends Youth Ambassador program to support youth in raising awareness of JA and other rheumatic diseases within their school community. Soleil is one of our first Team C+F Youth Ambassadors! This month she will give a presentation to her entire school on Juvenile Arthritis and [...]
For Lupus Awareness Month, we asked new C+F Board Member, Dr. Deborah Levy, to share five facts about childhood-onset Systemic Lupus Erythematosus (cSLE). Dr. Levy is the Clinical Director, Division of Rheumatology at the Hospital for Sick Children (“SickKids”) in Toronto and an Associate Professor of Pediatrics at the University of Toronto. She is the [...]
My name is Maryse Hendi and I live in Calgary, AB. In 2012, at age 10, I was diagnosed with lupus. Lupus is a disease in which the immune system becomes hyperactive and attacks healthy tissue, joints, and organs in the body. On May 1st, I celebrated a milestone in my lupus journey: my [...]
At Cassie + Friends, we're transforming kids’ lives and an A+ team. As National Manager, Events and Fundraising, you be a real champion for kids and families affected by Juvenile Arthritis (JA) and other childhood rheumatic diseases. You'll drive revenue growth coast-to-coast by executing our national annual giving strategy, fuelling peer-to-peer fundraising and not being [...]
Meet Sheila and Jim! They've shared their family’s journey with the rare rheumatic disease, CRMO, below. Sheila and Jim live in Qualicum Beach on beautiful Vancouver Island. They have three sons, two of which live with Chronic Recurrent Multifocal Osteomyelitis (CRMO). Nolan was diagnosed with CRMO at the age of five in [...]
The quarterly clinic in Prince George for kids with juvenile arthritis is a saving grace for some families. For others, it's one of a handful of options for specialized treatment. This article was originally published by the Prince George Post on Mar 14th, 2022 written by Matt Scace. When Cheryl Abraham’s son accidentally fell [...]
Addie, Prince George, BC 14 years old, Psoriatic JIA I used to hike and play school sports like basketball and volleyball. Now, I’m not able to because my arthritis hurts too much in my elbow, ankles and knees. This last year I started on the volleyball team, but had to stop playing because of [...]
Meet Carrie Ritchie! Carrie is a member of the Cassie + Friends National Board of Directors and a parent of a child with Juvenile Idiopathic Arthritis. We caught up with Carrie to learn about her family's journey with juvenile arthritis over the last 2 years. As a board member, Carrie looks forward to helping [...]
Scarlett’s journey started at about 16 months old. We noticed that in the mornings, she would just sit for up to two hours. Did not want to stand or walk - she almost seemed like she had to ‘warm up’ first. After about a week of no improvement, I took her to the doctor [...]
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