July 2025

Navigating Morphea – Michelle’s Story

By |July 15th, 2025|#KidsCantWait, Advice, Blog, Canada, Methotrexate, Morphea, Ontario, Rare Disease Stories, Stories, Toronto|

Navigating Morphea – Michelle’s Story For most of my life, I’ve had Morphea. Starting as a red mark on my chin as a young child, it eventually turned darker and over the years, spread to areas on my forehead, and neck. Morphea, also known as localized Scleroderma, is [...]

June 2025

Growing up with JDM – Layla’s experience

By |June 6th, 2025|Advice, Blog, Canada, JDM, Montreal, Quebec, Stories|

Growing up with JDM - Layla’s experience My experience with the healthcare system started earlier than most. I was diagnosed with Juvenile Dermatomyositis (JDM), a rare autoimmune disease that affects the muscles and skin, and since then, the Montreal Children’s Hospital has been a constant part of my life, [...]

April 2025

January 2025

#VirtuallyAnything

By |January 31st, 2025|Canada, Fundraising, Virtually Anything, Volunteer|

Are you ready to take action for kids living with Juvenile Arthritis (JA) and other rheumatic diseases? Make an immediate impact on childhood rheumatic diseases by doing #VirtuallyAnything to help raise awareness, fund research, and support families. The problem: Awareness of rheumatic conditions in youth is extremely low—only about 20% of Canadians are [...]

December 2024

A Year of Advocacy and Impact: Our 2024 Highlights

By |December 30th, 2024|Advocacy, Blog, Canada, News, Research|

A Year of Advocacy and Impact: Our 2024 Highlights If it seems like we were everywhere this year - we were! We never turn down an opportunity to raise awareness about childhood rheumatic diseases or advocate for more resources for our community. That’s what makes Cassie + Friends the leading voice for [...]

October 2024

Introducing Our New Parent Ambassadors!

By |October 17th, 2024|Blog, Canada, Fundraising, Hamilton, Ontario, Toronto, Volunteer|

We are so excited to introduce you to our newest parent ambassadors, Tamara and Bobby-Jo, from our McMaster and SickKids centres! Our parent ambassadors are often the first point of contact for newly diagnosed families and are there for anyone who might be struggling or need a hand finding resources. They [...]

August 2024

A Canadian Registry for Autoinflammatory Diseases: The CAN-SAID Initiative

By |August 22nd, 2024|Canada, Rare Disease, Research|

A Canadian Registry for Autoinflammatory Diseases The CAN-SAID Initiative Great news for Canadian autoinflammatory patients of all ages: Canada is getting its own registry for systemic autoinflammatory diseases! What exactly is a systemic autoinflammatory disease? Systemic autoinflammatory diseases (SAID) currently include over 50 rare conditions that are caused by uncontrolled [...]

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