There is no current cure for IgAN and that is why the IgA Nephropathy Foundation of America was
founded. Since the disease varies from one person to another, there is no definite progression or
course that the disease will take. What works for one person may have virtually no effect on
another, but our goal is to bring those with IgAN together to share experiences and bring
awareness to this disease.
Since there is no cure, treatments focus on slowing the progression of the disease and preventing
complications. Some individuals experience complete remission, while others live normal lives with
medications to treat their symptoms (such as high blood pressure meds, immunosuppressants,
omega 3 fatty acids & vitamin E supplements), yet others experience complete kidney failure
(end-stage kidney disease) and require either dialysis or a kidney transplant depending on the
severity. It is estimated that as many as half of those affected with IgAN will develop end-stage
renal disease. This poses one large problem… there aren’t enough kidneys and many patients wait
on the transplant list for years.