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IgANCare Program

Welcome to IgANCare – Your Trusted Network for IgA Nephropathy Support!

The IgANCare program is dedicated to improving the lives of individuals with IgA Nephropathy. Our mission is to connect patients with specialized healthcare providers who understand the unique challenges of this condition. 

We’re here to empower both patients and healthcare providers in the fight against IgAN. Together, we can make a difference in the lives of those affected by this condition. 
Ready to get started? Click the link below to join our network or connect with an IgAN specialist now.

For Patients

Finding the right healthcare provider for your IgA Nephropathy is crucial. IgAN Care simplifies the process, connecting you with qualified experts who can provide personalized care. No more searching endlessly; we’ve got you covered. 

Benefits for Patients:

  • Easy access to a network of IgAN-specialized healthcare providers. 
  • Peace of mind knowing you’re in the hands of experts.
  • Supportive community and resources to help manage your condition. 

Please revisit this page regularly, as we are continuously evaluating healthcare providers. We also welcome our patient community to refer their existing provider to our site or enter their information on this form and our team will reach out to confirm eligibility.

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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 before being correctly diagnosed with IgAN. For many, the condition had been misdiagnosed for an extended period of time, which could have resulted in preventable declines in their kidney function. 
A fair number were unsure of their stage of disease, which has important implications for treatment and life decisions. We can take action to improve patient diagnoses.

As part of our mission to build a support network, we have created the “IgANCARE” program, which will serve as a medical provider resource for patients with IgA Nephropathy. We are actively looking for Nephrologists willing to participate in this program. There is no cost to participate, and your participation will help improve the lives of our patients living with IGA Nephropathy.

We ask that you consider joining us and help our community of IgAN Patients. If you have any questions, please contact us at info@igan.org

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(848) 298-4618

PO Box 1322 Wall, NJ 07719

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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