Leadership Team

In 2004, Bonnie’s son Eddie was diagnosed with IgA Nephropathy. After finding a lack of information available and hearing that there was no ongoing research to find a cure, she quit her job in marketing and started the IgA Nephropathy Foundation with her husband, Ed. Bonnie works full time as …

Alena is a care partner to an IgAN warrior. In 2019, her wife, Gisela, received a kidney after being diagnosed with IgA Nephropathy at an early age. Alena joined the Foundation alongside Gisela. She works closely with the founder and pharmaceutical companies as well as patients and care partners to …

Stuart and his wife live in Georgia. Stuart has IgA Nephropathy and had a living donor transplant from his wife Carole through the paired exchange program. Stuart leads the foundation’s strategic planning, ensuring we meet and exceed our goals for success. stuart@igan.org

Gisela was diagnosed with IgA Nephropathy at the age of 14. Ultimately, it led to her kidney failure at the age of 38, requiring a kidney transplant. Luckily, she was able to avoid dialysis and received a pre-emptive transplant from her brother. Today, she wears many hats with the Foundation, but …

Carlos was diagnosed with IgA Nephropathy in 2015 when he was 30 years old. In 2016, after doing both peritoneal and in-center hemo dialysis, he received a living donor transplant from his younger brother. Today, he lives with his wife and dog in Northern Virginia. Carlos works full time as a …

Kate was diagnosed with IgA Nephropathy in the summer of 2019 at the age of 20. After undergoing several different treatments, including steroids and chemotherapy, her disease is still uncontrolled. Sitting in Stage 3 she is still hopeful to find a treatment plan that will work for her. Kate is …