08/31/2026
A family’s search for support became a mission to ensure no one else would have to navigate nephrotic syndrome alone.
This week’s Member Spotlight features Andi Callaway, founder and executive director of the Nephrotic Syndrome Foundation. Andi shares how her son’s diagnosis at age six inspired the organization’s creation and opened her eyes to the challenges families can face when they lack connections, resources, or accessible information.
Since 2017, the Nephrotic Syndrome Foundation has supported those diagnosed with nephrotic syndrome, their families, and the ongoing search for a cure.
Watch to learn how Andi’s family journey grew into an organization built around connection and support.