Wherever you are on your IgA Nephropathy (IgAN) journey, you belong here. Join our monthly Patient Support Group to connect with others who truly understand what it’s like to live with IgAN. Whether you’re newly diagnosed, managing treatment, living with stable disease, or facing new challenges, this virtual gathering offers a welcoming space to share …

Caring for someone with IgA Nephropathy (IgAN) comes with unique challenges, questions, and emotions—but you don’t have to navigate them alone. If you know and care for someone living with IgAN, we invite you to join our monthly Caregiver & Care Partner Support Group. This welcoming, virtual gathering is a safe space to connect with …

Each Congress, the IgA Nephropathy Foundation advocates for federal legislation to improve treatment options, foster innovation, and increase research funding for IgAN patients and the kidney community. We are heading back to Washington, D.C. Sept 29 – Oct 1, 2026 for our 3rd Hill Day and looking for patients/family members interested in attending. US based members only. Travel Assistance …