September 2024

True North Resilience: Kira Young’s Story

By |September 15th, 2024|Advocacy, Blog, MAS, Northwest Territories, Rare Disease, sJIA, Stories|

At Cassie + Friends, we believe that every child and family should have access to timely and optimal rheumatic disease care. That’s why we launched the C+F Northern BC Project, to better understand the barriers to diagnosis, care, and patient support for families living in remote/rural communities and explore how we can work [...]

May 2024

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 [...]

May 2023

Mental Health Matters: Kaese’s Journey With JA

By |May 5th, 2023|Advocacy, JIA, Mental Health, Mental Health (For Youth), Stories|

"Feelings and emotions are real, and should be felt and openly discussed." Meet Kaese and his mom, Jennifer. Together, they have chosen to share their story of being diagnosed with JIA and the many impacts that can have on a child and family's mental health. To read more Cassie + Friends' Youth Mental [...]

May 2021

May 2017

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