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 …
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 …
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 …
