Fireside Chat with NORD on the IgAN Patient Assistance Program

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A recap of Montrez Lucas’ interview with Jill Hollander, the Vice President of the National Organization for Rare Diseases (NORD), about the innovative IgA Nephropathy (IgAN) Patient Assistance Program.

During this engaging webinar, we reviewed NORD’s financial assistance program, exploring how it can provide crucial support for those affected by IgA Nephropathy. From assistance with insurance premiums and co-pays to aiding with diagnostic testing and offering travel support for clinical trials or consultations with disease specialists, NORD’s program was introduced as a valuable resource.

Watch this insightful and empowering webinar aimed to alleviate the challenges associated with managing IgAN by equipping participants with valuable information and resources. Stay tuned for more updates and be sure to subscribe for future webinars that provide ongoing support for the IgA Nephropathy community and visit our events page for upcoming webinars.