Join the only global patient organization exclusively focused on IgA Nephropathy.
Whether you’re an IgA Nephropathy patient or a loved one, you’re not alone in your journey. We welcome everyone to join our community regardless of financial means. Become part of our global family to learn and sharet, and to support one another. As a recognized 501(C)(3) non-profit, public health organization, the IgA Nephropathy (IgAN) Foundation is committed to research for a cure, public education, and patient service. To date, we have awarded almost $1,000,000 to fellowship grants for research into the causes and cure for IgAN. When you become an IgAN Foundation member, you’re not only gaining access to a trove of resources—you’re helping to support the IgAN community. Join our global family!

Basic Member Benefits (Free)

  • Monthly e-Newsletters
  • Access to IgA Nephropathy Foundation Educational Brochures
  • Access to IgA Nephropathy Foundation Facebook Groups
  • Access to IgA Nephropathy Clinical Trial Alerts
  • Information on local support groups
  • Participation in virtual meet-ups: Care partner meet ups and patient meet-ups
  • Opportunity to apply for patient aid through our financial support program

Champion Member Benefits ($60 annual)

  • All the benefits of basic membership plus:
  • Membership welcome packet with cool IgAN Foundation-branded merchandise, such as branded notebook and pen, IgAN Foundation decal and an official membership card
  • Discount on SPARK event and recognition lanyard
  • Member-only event invitations and other surprises
  • Help underwrite research grants to find a cure!
  • And more...

We DO NOT disclose or share your information with other entities. It is strictly used to communicate with you on behalf of the IgAN Foundation.

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