October 2024

Giving Tuesday

By |October 17th, 2024|Advocacy, Blog, Fundraising|

Be a Champion this Giving Tuesday Giving Tuesday is a day where people all over the world can do something together to make the world a better place. That’s pretty inspiring, and even more so when the cause is drastically under-represented and under-funded, like in the case of Juvenile Arthritis and childhood [...]

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 [...]

June 2024

May 2024

April 2024

Youth Mental Health Strategy Funding Announcement

By |April 10th, 2024|Advocacy, Blog, Current Research, Future Research, Home Page, Mental Health, Mental Health (Caregivers), Mental Health (For Youth), News, Research|

Youth Mental Health Strategy Funding Announcement       NEWS RELEASE Two Canadian teams awarded new funding to study mental illness in youth with rheumatic diseases. Brain Canada and Cassie + Friends unveil the recipients of the Addressing Mental Health in Paediatric Rheumatic Diseases Team Grants program. Source: Brain Canada MONTREAL, April [...]

March 2024

March is Juvenile Arthritis Awareness Month!

By |March 15th, 2024|Advocacy, CREW, Current Events|

Did you know that March is Juvenile Arthritis Awareness Month in Canada? Here at Cassie + Friends, we have been raising awareness and providing support to the JA community since 2007! We are the only charity in Canada exclusively dedicated to the pediatric rheumatic disease community and our dedication shows! From our Team Cassie [...]

October 2023

Seeing Possibilities after Diagnosis: a Uveitis Story

By |October 24th, 2023|About JIA, Advice, Advocacy, Blog, CREW, Rare Disease, Saskatchewan, Stories, Uveitis|

Throughout my life I have been granted many titles; mom, wife, daughter, registered nurse, and writer are just a few. These are the titles that are associated with my name. I could be described as outgoing, humorous, modest, and perhaps kind too. These would be some characteristics that people from a distance would use [...]

Mental Health Workgroup

By |October 17th, 2023|Advocacy, Mental Health, Mental Health (For Youth), Research|

National Pediatric Rheumatology Mental Health Workgroup Cassie + Friends has led the formation of a new workgroup on Pediatric Rheumatology Mental Health to improve mental health care and outcomes for children with rheumatologic diseases. The goal of this Mental Health Workgroup is to develop strategies to improve research, care, and outcomes about mental [...]

August 2023

C+F Inventing Room: Reinventing the Injection Experience for Kids and Families Affected by JA and other childhood rheumatic diseases in Canada

By |August 31st, 2023|Advice, Advocacy, Blog, Injection, Medication|

Inspired by the Roald Dahl Charity’s Marvellous Nurse Inventing Rooms, on August 23rd, we hosted our very own C+F Inventing Room to ask the community and together envision what our C+F Injection Coping Kits should include. With the help of medical experts, parents and youth, we dove in and got to work! We started [...]

June 2023

Get to know our Youth Ambassador of of the Year, Alejandra Van Dusen

By |June 8th, 2023|Advocacy, Mental Health (For Youth), Post- Secondary, Stories, Teen Transitions|

“As a young adult with JIA I have experienced firsthand just how much goes on at this age. School, work, relationships, newfound independence, transition… I wanted to create resources with short pieces of patient-driven advice to help others like me navigate the constant changes of life with rheumatic disease.” [...]

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