New Clinical Research Option for Recurrent C. diff Patients
Due to the nature of C. diff infections, particularly the high recurrence rate following standar…
PLF in the News – The Incredible Genesis of C. diff Advocacy
In the latest from ContagionLive, John Parkinson sits down with PLF CEO Christian John Lillis to…
Proudly Introducing the Peggy Lillis C. difficile Inclusion Act
On July 23, Congresswoman Yvette Clarke (D-NY) introduced H.R. 9008 Now we are urging Congress, …
PLF in the News – Advocate Minnie Hatch Shares Agonizing C. diff Story with Self.com
Too Young for C. diff
C. diff survivor and long time Peggy Lillis Foundation advocate, Mi…
Empowering Change: Highlights from the 9th Annual C. diff Advocacy Summit & Lobby Day
On April 15th, Peggy Lillis Foundation convened its ninth annual National C. diff Advocacy Summi…
You can be a savior
This was adapted from my 2024 National C. diff Advocates Summit speech.
My mother was many th…
Welcoming Paul Feuerstadt, Debbie Trinker, and David Shlaes to Our Board of Directors
On February 5, we announced the appointment of Paul Feuerstadt, MD; Debbie Trinker, BA, JD; and …
Navigating the Challenges Together: Tackling C. diff with the Power of Peer Support
Peggy Lillis Foundation’s Peer Support Network is an online program for people affected by Clost…
2023 “See C. Diff” Reaches 23 Million People!
We did it! Once again, the Peggy Lillis Foundation for C. diff Education and Advocacy (PLF) surp…
PLF in the News: Advocate Jenny Feldman Sits Down with Pharmacy Times
PLF Advocate and C. diff survivor, Jenny Feldman, sits down with Pharmacy Times to discuss navig…
2023 Changing the Odds Gala Raises $110,000 for C. diff Education and Advocacy
On Friday, November 3rd, Peggy Lillis Foundation (PLF) held its 14th Annual Changing the Odds Ga…
PLF in the News: Advocate and Board Member Carol Raye Featured On KevinMD
C. diff survivor, Patient Advocate, and Peggy Lillis Foundation Board Member, Carol Raye, has a …