IgA Nephropathy Foundation Recognized for Leadership and Research Excellence at ASN Kidney Week 2025
Bonnie Schneider delivers keynote at ASN Kidney Week 2025 as Foundation debuts first research poster and hosts IgAN therapies forum.WALL TOWNSHIP, NJ, UNITED STATES, November 6, 2025 /EINPresswire.com/ — The IgA Nephropathy Foundation proudly marked a milestone presence at this year’s American Society of Nephrology (ASN) Kidney Week, held November 5–9 in Houston, Texas. Through a series …
Building community following a rare kidney disease diagnosis: Ruchi’s story
Patient Voice spoke with Ruchi Ambike about her search to find community after being diagnosed with a rare disease. “I had just started my master’s program in 2001 when a routine physical led me to be diagnosed with IgA nephropathy, a rare auto-immune disease of the kidneys. Honestly, I didn’t really worry about it at …
IgA Nephropathy Foundation Announces the Launch of Go Global Network to Support for IgA Nephropathy Patients Worldwide
Expanding Global Support: IgA Nephropathy Foundation Launches Go Global Network to Connect and Empower IgAN Patients Worldwide. By expanding our network to Canada, we are building a stronger, more connected global community dedicated to advocacy, education, and support.” — Bonnie Schneider TORONTO, ONTARIO, CANADA, April 21, 2025 /EINPresswire.com/ — The IgA Nephropathy Foundation is proud to announce …
IgA Nephropathy Foundation Celebrates 20 Years of Advocacy, Research, and Patient Support
WALL TOWNSHIP, NJ, UNITED STATES, March 18, 2025 /EINPresswire.com/ — The IgA Nephropathy (IgAN) Foundation marks its 20th anniversary in 2024, celebrating two decades of groundbreaking efforts in research, patient advocacy, and community building. Founded in 2004 by Bonnie and Ed Schneider after their son’s IgAN diagnosis, the Foundation has grown into a global leader in supporting …
