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 [...]