Katie Moss

Katie Moss is a patient parent that lives in Portland Oregon. Her daughter was diagnosed at two with Minimal Change Disease. She found NephCure through her physician and has been an active participant since. She was glad to have found an organization like NephCure that educates and provides a sense of community to those that are going through the journey of Rare Kidney Disease.

NephCure Email: katiemoss@nephcurevolunteer.org

Oregon