Membranous Nephropathy Day: Let’s Talk MN

🚨 MN AWARENESS DAY — FULL CONVERSATION NOW AVAILABLE Our Membranous Nephropathy Awareness Day livestream didn’t reach everyone as planned tonight — so we’re making sure the FULL conversation is available right here on YouTube. No edits. No highlights. The complete conversation. In recognition of Membranous Nephropathy Awareness Day, The Enlisted Kidney Foundation and NephCure brought together patient advocates Seferiana Day and Dan Holmes for an honest conversation about what living with MN actually looks like. We talk diagnosis. Treatment. Setbacks. Transplantation. Self-advocacy. Finding the right care. And what it takes to keep moving forward when you’re living with a rare kidney disease. If you registered for tonight’s event but weren’t able to get in — this is your chance to watch. And to our West Coast kidney warriors — MN Day isn’t over yet. We’re here. Whether you’re newly diagnosed, have been living with MN for years, care for someone with the disease, or simply want to understand it better, this conversation is for you. Watch now. Share it with another kidney warrior. And help us close out MN Awareness Day together. Presented by The Enlisted Kidney Foundation × NephCure No kidney patient should ever navigate this journey alone. #MembranousNephropathy #MNAwarenessDay #NephCure #EnlistedKidneyFoundation #FilterLIFE #KidneyDisease #RareKidneyDisease #KidneyWarrior