January 2025

Paige’s Journey with Juvenile Idiopathic Arthritis

By |January 6th, 2025|Advocacy, B.C., Blog, JIA, Stories, Vancouver|

Paige’s Journey with Juvenile Idiopathic Arthritis To have a chronic illness is to be fighting every day for the next. My name is Paige Simpson. I am 17 years old, I was diagnosed with Juvenile Idiopathic Arthritis, otherwise known as JIA. I have been treated for JIA for 15 years but have [...]

December 2024

A Guide to Accommodations: Acceptance, Peer Pressure, and Fear

By |December 16th, 2024|Advice, Blog, High School, Post- Secondary, Work + Careers|

A Guide to Accommodations Acceptance, Peer Pressure, and Fear We’re honoured to share this piece by Kayla Caddy, a young adult living with Juvenile Idiopathic Arthritis (JIA) who works as a job coach for people on the autism spectrum. Drawing on her lived experience and professional expertise, Kayla shares with us [...]

June 2023

Tough as Nails: A Father Reflects on his Two Daughters and Childhood Rheumatic Disease

By |June 5th, 2023|Advocacy, High School, JIA, Post- Secondary, Rare Disease, Stories, TMJ|

"We're very proud of our girls for showing the fortitude needed to not let these diseases define them." Hello families! My name is Mike Wiens, husband to Jesica and father to two girls, Vanessa 24 yrs old, and Sarah 23 yrs old. We're happy to call Port Moody, BC our home since relocating here [...]

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