The C Diff Foundation, a 501(c) (3) non-profit organization, established in 2012 and dedicated at supporting public health through education, support, and advocating for C. difficile infection (CDI) prevention, treatments, and environmental safety worldwide.
The Foundation’s founder is a Nurse and after suffering through C. difficile infections herself and witnessing the loss of their Father, whose life was claimed by C. difficile involvement, the C Diff Foundation came to fruition.
The C Diff Foundation Members with their Volunteer Patient Advocates successfully “Raise C. diff. Awareness” nationwide and in thirty-eight countries and hosts a U.S. Nationwide information Hot-Line (1-844-FOR-CDIF) to support health care providers and patients to manage through the difficulties of a C. diff. infection among many other programs.
The continued support of the Foundation’s mission is through collaborative efforts from healthcare providers, medical healthcare organizations, healthcare professionals, government agencies, employers, and communities, which will bring positive results in the reduction of newly diagnosed Clostridium difficile cases and preventable deaths.
Nearly half a million Americans suffer from Clostridium difficile (C. diff.) infections in a single year according to a study released February 25, 2015 by the Centers for Disease Control and Prevention (CDC).
C Diff Foundation™ is a trademark of The C Diff Foundation, established 2012 in the U.S.
