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  • IgAN
    The IgA Nephropathy Foundation’s mission is to be a patient-centric organization focused on finding a cure for IgA Nephropathy
  • IgANCare Program | IgA Nephropathy Foundation
    Find an IgAN Health Specialist For Healthcare Providers The IgA Nephropathy Foundation is a patient-centric 501 (c) (3) charitable organization focused on finding cures for IgA Nephropathy There is an urgent need to raise awareness about IgAN, including how it differs from other chronic kidney conditions, and to help assure more timely diagnoses Nearly half of patients (48%) faced delays
  • What is IgA Nephropathy? [Immunoglobulin A (IgA)] Learn Here
    IgA Nephropathy (IgAN) is an autoimmune disease that attacks the kidneys It affects how blood is filtered in the small blood vessels of the kidneys IgAN occurs when an abnormal protein damages the filtering unit (glomerulus) inside the kidneys It is estimated that 20-40% of the people who have IgAN will develop end-stage kidney disease, which means they will need dialysis or kidney
  • IgAN Ambassadors | IgA Nephropathy Foundation
    IgAN Ambassadors Our Ambassador Team Find an Ambassador Near You IgA Nephropathy (IgAN) remains poorly understood For far too many people, the journey with IgAN is a struggle, often filled with misinformation, sometimes years of medical uncertainty, or not knowing where to turn It’s easy to feel alone and isolated We are set to change this!
  • Go Global Canada | IgA Nephropathy Foundation
    Go Global Canada In Canada, the incidence of IgAN is 1 6 per 100,000, and approximately 260 Canadians are diagnosed yearly As part of the IgA Nephropathy Foundation’s Go Global initiative, we’ve expanded our advocacy and educational efforts into Canada to address the urgent needs of patients navigating limited treatment options
  • Igan Basics | IgA Nephropathy Foundation | February 17, 2021
    There is a lot of technical language around IgAN and it can seem confusing and overwhelming when receiving a diagnosis for yourself or a loved one You may | IgA Nephropathy Foundation February 17, 2021
  • Go Global Australia | IgA Nephropathy Foundation
    As part of The IgAN Foundation’s expansion, the Go Global Network will establish a stronger presence in Australia, fostering new partnerships and resources to support Australian IgAN patients and their families
  • Diagnosed with IgA Nephropathy? What You Need to Know
    Diagnosed with IgA Nephropathy? What You Need to Know If you or a loved one has been diagnosed with IgA Nephropathy, also called IgAN for short, it’s normal to feel scared or uncertain
  • IgAN FAQs
    IgAN was thought relatively benign when it was first identified in 1968 by the French doctor, Jean Berger, but gradually researchers realized that in up to 50% of the cases, the disease very slowly progresses to end-stage renal failure, requiring major lifestyle changes, dialysis, and possibly transplantation





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