Melissa Baumbick is the CEO of the Facial Pain Association, a rare disease patient advocacy organization with a 35-year legacy. She brings more than a decade of nonprofit experience, following 17 years in corporate and small business marketing. Melissa combines strategic vision with deep expertise in brand development and communications; all grounded in a strong commitment to mission-driven work. Her passion for serving those affected by rare conditions drives her efforts to raise awareness, build community, and create lasting impact.
