Megan Madison
Dedicated Advocate, Diagnosed with Granulomatosis with Polyangiitis (GPA)
Megan Madison’s journey with vasculitis is one of resilience, perseverance, and turning personal challenges into meaningful action. After nearly a decade of unanswered questions and misdiagnoses, she was diagnosed with Granulomatosis with Polyangiitis (GPA) in 2023—finally gaining clarity after years of uncertainty.
Rather than facing that journey alone, Megan chose to help others do the same. Motivated by her experience, she became a dedicated advocate—sharing her story, organizing fundraising events, and raising awareness so others can find answers and support sooner. “I didn’t want another person to feel alone in their journey,” she shares, a mission that continues to guide her work.
Through the Vasculitis Foundation, Megan found connection both locally and nationally, building relationships that have become a vital support system. Today, she continues to strengthen that community—helping others navigate diagnosis, find encouragement, and keep moving forward with hope.