NephCure's Dr. Blair Kiser leads this NephCure U webinar focusing on 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.

Listen and 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!