Thank You
We would like to thank you for visiting our page. Our mission is to raise funds for the Alport Syndrome Foundation so that children like Norah can have access to education, awareness, and new treatments for Alport Syndrome. Please click below to learn more about what we do.
About MCKF
Norah Dunlap was born with Alport Syndrome, a rare genetic disorder that leads to hearing loss, eye abnormalities, and eventual kidney failure. Her father, John Dunlap, also affected by the condition, discovered a supportive network of families through the Alport Syndrome Foundation. Inspired by their experiences, John and Norah organized the Music City Kidney Fundraiser to support the Foundation and other families dealing with Alport Syndrome. To learn more about the Alport Syndrome Foundation, click below.