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Celebrate Kidney Month this March

Spread the word: we deserve equitable care for every rare kidney disease

March is National Kidney Month, and we invite you to raise awareness about rare kidney disease. For too long, these conditions have been underrepresented, with advancements driven largely by the courage and advocacy of patients and families themselves. This March, we invite you to add your voice to the cause. Together, we can ensure that all individuals with rare, protein-spilling kidney disease have equitable access to the care and treatments that offer them the best kidney health outcome possible. 

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Access to Equitable Kidney Care Starts Here

For more than 25 years, NephCure has worked alongside patients, caregivers, researchers, industry partners, and physicians to transform the rare kidney disease landscape. When NephCure was founded, there was little scientific understanding of rare kidney disease, no FDA-approved treatments, and almost no therapies in development.

Today, that story is changing. Together, this community has helped make six FDA-approved treatments possible, supported more than 60 clinical trials, and built a network of over 40,000 families who have found knowledge, hope, and connection. 

As scientific breakthroughs accelerate, NephCure recognizes FDA-approved treatments are not the finish line, but rather the starting line. Too many families still face barriers: late diagnosis, difficulty finding expert physicians, and inequities that delay or block access to care and new treatments. To meet this moment, NephCure introduces its new mission statement:

Our New Mission: 

To ensure that all individuals with rare, protein-spilling kidney disease have equitable access to the care and treatments that offer them the best kidney health outcome possible.

Your Story Matters 

Sharing your experience helps others feel less alone and builds greater awareness and understanding of rare kidney diseases. We feature patient stories across our social media, newsletter, and website to educate, inspire, and connect our community. 

Help Us Spread Awareness This Kidney Month

Download the toolkit
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Patient Voices

C1q Nephropathy (C1q), Focal Segmental Glomerulosclerosis (FSGS)

Alyssa K.

My daughter, Alyssa, was at her 4-year checkup when her pediatrician informed me that her blood work showed high cholesterol. He referred us to a cardiologist, and for nine months, …

Focal Segmental Glomerulosclerosis (FSGS), Nephrotic Syndrome

Ruth S.

My FSGS story so far  In trying to put words down to tell my story, I needed to remember things I’d squashed and put aside for self preservations sake. Being …

Minimal Change Disease (MCD), Nephrotic Syndrome

Anthony S.

Anthony, my 5-year-old son, has been battling minimal change nephrotic syndrome since he was 2. Diagnosed after a bizarre swelling episode post-COVID, he’s become the “head-scratcher” for doctors due to …

Focal Segmental Glomerulosclerosis (FSGS)

Marcelo P.

I share my story to offer hope and remind others they’re not alone.  It’s ironic—almost poetic—that March is both Kidney Month and my birthday month. It’s also the month that, …

Focal Segmental Glomerulosclerosis (FSGS), Nephrotic Syndrome

Melissa M.

Seferiana Day was diagnosed with Primary Membranous Nephropathy and Stage 1 Chronic Kidney Disease in February 2016. An otherwise active and healthy 30 year old…

Membranous Nephropathy (MN)

Dan H.

Dan is from Baltimore, MD. Who is living in Florida and served in the US NAVY from 2003 to 2008 as a Special Operations Search and Rescue Veteran that was …

Membranous Nephropathy (MN)

Seferiana D.

Seferiana Day was diagnosed with Primary Membranous Nephropathy and Stage 1 Chronic Kidney Disease in February 2016. An otherwise active and healthy 30 year old…

Shop With Purpose

We Want your Feedback

NephCure is launching a short patient survey to better understand the needs of our community. We want to make sure that we are providing the right tools to the rare kidney so that patients and families have the support, information, and resources they need. 

By sharing your voice, you help NephCure amplify the real patient experience in rare kidney disease, identify the biggest unmet needs in the community, guide research priorities and advocacy efforts, and improve education and support for patients and families.

complete the survey

Advocate With us on the Hill

This Kidney Month, use your voice to drive meaningful change for people living with kidney disease by joining us in Washington, DC for Rare Kidneys on the Hill Day.
 
Rare Kidneys on the Hill Day is an opportunity for advocates to raise awareness about rare kidney disease and to make their voices heard by their members of Congress on issues that impact their lives. Anyone impacted by RKD is invited to join us – patients, caregivers, physicians, and researchers are welcome! 

sign up for hill day

NephCure’s 2025 Impact

Our 2025 impact report highlights significant strides in research advancement, expanded clinical trial access, and enhanced patient support for rare protein-spilling kidney diseases. It reflects the organization’s growing specialist network and continued progress toward developing better treatments and ultimately finding a cure.

Read more

Make a Difference This Kidney Month

Want to do more than raise awareness? Become a NephCure volunteer and help strengthen our rare kidney disease community. Whether you’re passionate about supporting patients, sharing your story with researchers and policy leaders, advocating for change, or helping at events, there’s a meaningful way for you to get involved. Volunteers play a vital role in spreading hope, building connection, and driving progress for people and families affected by rare kidney disease. This Kidney Month, your time and voice can make an even bigger impact. 

become a volunteer
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Resources That Expand your Access to Care 

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Newly Diagnosed

Newly Diagnosed?

For so many people, coping with a recent diagnosis of rare kidney disease means feeling afraid, worried, or even alone. Take back your health and your hope by understanding your disease. We’ve compiled these introductory resources to help get you started.

START HERE
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Find a Specialist

Find a Specialist

The understanding of rare kidney disease evolves every day. To provide the best care possible, NephCure Specialists stay on the cutting edge of the latest research, treatment options, and clinical trials, while sharing resources with the RKD community. Better care is only a click away.

FIND A SPECIALIST
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Clinical Trials

Explore Treatments Currently In Trial

The world of RKD therapies is evolving fast. As scientists and medical professionals learn more about rare, protein-spilling kidney diseases, patients everywhere gain access to clinical trials for the best care possible and latest treatment options. Learn more to see if you or a loved one would be a good fit for one of the current trial opportunities.

SEE CLINICAL TRIALS
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Get Support Now

Get Support Now

Not sure where to begin? For more than 20 years, NephCure has helped RKD patients and their loved ones navigate the ins and outs of these challenging diseases. Reach out today and we’ll welcome you into our community, guiding you to the resources you need.

Get Support

Thank You to Our 2026 Kidney Month Sponsors

Thank you to our NephCure Corporate Members who are our valued partners for Kidney Month and World Kidney Day Campaigns.  Their generous support enables NephCure to develop programs, events and educational resources to pursue our mission of ensuring access to the care and treatments that offer patients the best kidney health outcome possible. 

In Partnership With

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