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Welcome to your IgAN family.

Whether you or someone you love has been diagnosed with IgA Nephropathy, you have come to the right place. You are not alone.

By patients, for patients

The IgA Nephropathy Foundation’s mission is to be a patient-centric organization focused on finding a cure for IgA Nephropathy. Using the power of the patient community, we are focused on funding research, using patient advocacy to empower our patients, and building a network of support.

Latest News & Resources About IgAN

Ambassador Program

The IgA Nephropathy Foundation Ambassador Program will bring together and train a select group of inspired patients and caregivers.

Ambassador Program

Guides & Fact Sheets

Use this guide to learn more about IgA Nephropathy, including common tests used to check your kidney health, what to look for and expect at different stages, and various treatment options.

Guides & Fact Sheets

International IgAN Network

Learn more about the International IgA Nephropathy Network. For Clinicians and Patients with IgA Nephropathy.

More About IIgANN

IgAN Cookbook

We are so pleased to offer our first-ever cookbook devoted to patients and caregivers of IgA Nephropathy.

IGAN Cookbook

“Knowing you’re not alone is very powerful. So is knowing it’s not fully out of my control and I can take steps every day to help.”

CHRIS

IgA Nephropathy Facts

What is IgA Nephropathy?

IgA Nephropathy (IgAN) is a rare, 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 transplantation to survive.

How is IgA Nephropathy Diagnosed?

The first sign of IgAN is often blood in the urine. Should this occur, you should immediately consult your doctor.

How is IgA Nephropathy Treated?

There is no current cure for IgAN and that is why the IgA Nephropathy Foundation was founded.

Explore More FAQ’s

Faces of IgA Nephropathy

Our mission is to be a patient-centric organization focused on finding a cure for IgA Nephropathy. Using the power of the patient community we are focused on funding research, using patient advocacy to empower our patients, and building a network of support.As a patient run organization, we will work together with the hope of finding better treatment options and ultimate cure. By patients, for patients.

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Contact Us

(848) 298-4618

(732) 681-3462

PO Box 1322 Wall, NJ 07727

© 2023 All Rights Reserved.

May 14, Sunday: Mother’s Day & IgA Nephropathy Awareness Day

The IgAN Foundation was sparked by a mother’s love and has grown into a community sharing crucial resources and working toward a cure. This day kicks off a week of celebrating the IGA Nephropathy family all week!

May 15, Monday: Mindfulness

IgA Nephropathy can be challenging and mindfulness is an important part of caring for yourself. Take a moment today and implement a mindfulness practice, meditate, or take a few moments in reflection to check in with yourself.

May 16, Tuesday: Share Your Story

On this day, the Foundation will share the video with Warrior stories compiled (submit yours here if you haven’t yet). We encourage you to also share your own photos and videos from moments along your journey!

May 17, Wednesday: Wellness

What are you doing to feel well today? IgA Nephropathy can sometimes make life feel uncontrollable, but there are some things we can control, for example:

  • Enjoyable movement (a stretch, a walk, dancing to a favorite song)
  • Eating food that’s right for us individually
  • Checking in with ourselves
  • Meditating

May 18, Thursday: Thank those who care

Between care teams, care partners, and medical providers, a lot goes into the care that sustains us as we live with IgA Nephropathy. Take this opportunity to express your appreciation to them!

May 19, Saturday: Rally cry

When the IgA Nephropathy Foundation was created, there were no resources to treat IgA Nephropathy. Now, there are 2 approved FDA treatments and many clinical trials in the works. Our community is strong and full of hope— here’s to even more progress in the future!

May 20, Saturday: Celebration! 

We’ll be hosting an in-person celebration (details to come). We’ll miss you if you can’t make it, but please take the time to celebrate however works for you — wearing your IgAN Foundation sunglasses, spending time with loved ones, etc. — just be sure to share a photo and tag us!

References

  • Hall, Y.N., Fuentes, E.F., Chertow, G.M. et al. Race/ethnicity and disease severity in IgA nephropathy. BMC Nephrol 5, 10 (2004). https://doi.org/10.1186/1471-2369-5-10
  • Kiryluk K, Li Y, Sanna-Cherchi S, Rohanizadegan M, Suzuki H, et al. (2012) Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis. PLoS Genet 8(6): e1002765. doi:10.1371/journal.pgen.1002765