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Join Our Team: We Can For IgAN [Under Family Team]
The IgA Nephropathy Foundation began with concerned parents Ed and Bonnie Schneider from Wall Township, NJ determined to make an immediate impact. In 2004, when Ed and Bonnie Schneider’s son was diagnosed with IgA Nephropathy (a rare, autoimmune kidney disease) at age 13, she had nowhere to turn for resources and patient support. She and her husband launched the Foundation from their kitchen table in hopes of helping others like them and funding further research on this rare, chronic kidney disease.
Annually, around 25 people per million worldwide are newly diagnosed with IgAN. There is currently no cure for IgAN, and treatment is focused on managing symptoms, controlling blood pressure, and slowing the kidney disease process.
The IgA Nephropathy Foundation is committed to research for a cure, public education, and patient service. Our growing IgAN community family is a testament to the need for our work and the strides we’ve been able to make. Make no mistake: We are going to find a cure. It may take time, but we will find it. As we work toward this goal, we are here for you and your family — at every step of your journey.
YOU ARE NOT ALONE ❤️💙Learn More www.igan.org
100% of donations (unless otherwise designated by the donor) go toward IgA Nephropathy research.
Join Our Team: We Can For IgAN [Under Family Team]
