Fellow IgA Nephropathy Warriors, My Heart Aches with Yours 😔💔🫂 Dear friends, hearing about Fabhalta (Iptacopan) fills me with fragile hope and deep sorrow... Hundreds per pill, tens of thousands monthly 💊💸😢. For ordinary families battling IgA nephropathy—managing proteinuria, clinging to kidney function—this cost feels crushing, utterly out of reach. Those sleepless nights wondering how long we can hold on... I feel your pain so deeply. You're not alone. 🥺💧 Living with this for years means daily meds, strict diets, small victories in lower proteinuria. Fabhalta and over a dozen pipeline drugs offer real promise by targeting new pathways. Yet the price breaks our hearts—who can sustain this long-term? We desperately need affordable options and better coverage so no one loses hope over money. We deserve that. 🙏 How are you coping, dear warriors? Struggling with these costs? Share your story—we're here to hold each other up, through tears and strength. You're incredibly brave. Let's keep fighting together. 🌟💪🫂 I've found helpful drug info and price comparisons on DengYueMed—worth checking if you're seeking more affordable paths. Holding on with you. Brighter days will come. Endless hugs ❤️🤗 #IgANephropathy #KidneyWarriors #WeFightTogether #NewDrugPrices