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 [...]

October 2023

Lily’s Journey to Diagnosis, Methotrexate, and Finding A Community of Support

By |October 19th, 2023|Injection, JIA, Medication, Methotrexate, Newly Diagnosed, School, School Toolkit, TMJ|

Meet Lily. One morning, at the young age of 2, our daughter Lily woke up limping and her left knee looked slightly swollen. She didn't seem to show that she was in pain, but was refraining from putting weight on her left leg. We had no idea what happened and didn't recall any [...]

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