George & Ginny Dieruf
Founders, Board Members and Parents to Cody Nicole Dieruf
We lost our daughter, Cody, to Cystic Fibrosis at the age of 23. We miss her and she is in our hearts forever. The Cody Dieruf Benefit Foundation for Cystic Fibrosis keeps Cody's legacy alive and at the same time we are able to help out other families affected by Cystic Fibrosis.