My Nonprofit Reviews

In 2012 my daughter was diagnosed with IgA Nephropathy. I had no idea what this disease was! I googled and googled and found the IgA Nephropathy Foundation of America. I poured over their website and then sent a donation. From there, Bonnie, the Founder, contacted me. We are working hard to provide resources for other families like us as well as raise money for research. There is still so little known about this disease and every dollar raised by the IgAN Foundation goes toward researching this horrific disease. I encourage anyone affected by IgA to reach out to this Foundation! The Board can put you in touch with others in your area that are also affected which is tremendously helpful when you don't know where to turn. I am both a client served and volunteer.