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Living Beyond Limits with IgA Nephropathy

IgA nephropathy (IgAN) may reshape your path, but it doesn’t define your destination.

Your experience with IgA nephropathy holds power to comfort, enlighten, and inspire.

Share your “Me &” story to show how you live beyond limits with IgAN, reminding our community that we are each so much more than our diagnosis.

More Than a Diagnosis

IgAN is a rare kidney disease that affects approximately 1 in 100,000 people each year, silently building deposits of immunoglobulin A in the kidneys that can gradually affect their ability to filter waste. For many, the journey begins unexpectedly; perhaps with tea-colored urine or persistent fatigue that signals something isn’t right. While each experience is uniquely personal, the questions and uncertainties often echo across our community: navigating the complexity of symptoms that come and go, understanding test results that fluctuate, and finding ways to embrace life’s fullness despite the unpredictability of this condition.

Yet within these shared challenges lies our collective strength. We are more than individuals affected by a rare kidney disease—we are adventurers, dreamers, and champions of our own stories.

Finding Support

Your journey with IgA nephropathy doesn’t have to be walked alone. Dedicated advocacy organizations stand ready to illuminate your path with resources, community, and hope at every turn.

The IgA Nephropathy Foundation and NephCure have curated reliable resources and information specifically designed for our community. From educational webinars to peer connection programs, these organizations transform isolation into belonging and questions into empowerment.

Finding Support

Resources That Empower

Knowledge transforms challenges into pathways. Explore these carefully curated resources from our advocacy partners to strengthen your IgAN journey:

From the IgA Nephropathy Foundation:

Voices That Resonate: Community Stories

Every story shared creates ripples of possibility for someone else navigating life with IgA nephropathy. These voices from our community remind us that beyond the medical appointments and lifestyle adjustments, there are moments of joy, triumph, and everyday courage waiting to be celebrated.

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View full stories from real people

Tanya C.Tanya C.
IgAN

When I was first diagnosed it was very difficult to absorb. I was only 8…

Rachel M.Rachel M.
IgAN

You are so tough and smart. Your childhood medical challenges will help you later…

Sarah L.Sarah L.
IgAN

You, yes you, put that textbook down for a minute. I have some important words of…

María L.María L.
FSGS
IgAN

In this life you have to be strong, yes, oh yes! You are going to have to…