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Dr. Blair Kiser, NephCure’s Director of Government Relations & Advocacy, will share exciting news surrounding the NephCure Action Network, our government relations and grassroots advocacy program. Our goal is to advance legislation, funding, and awareness to ensure that patients with rare, protein-spilling kidney disease receive the support they need. Learn how you can transform your lived experiences as a rare kidney disease community member into an inspiring call-to-action to affect change nationwide!
