Thanks to the IgA Nephropathy Foundation of America we now have a new introductory packet for patients with IgAN. This guide does an excellent job of detailing what this rare disease is, how to best handle your diagnosis and treatment plan and what scenarios could potentially play out over time.

Since the IgAN experience can be different for each patient there’s no one size fits all approach to treatment, but there are some common recommendations in how we should best care for ourselves.

If you want to learn more about IgA Nephropathy please check out the guide at the following link: