96%
As a part of our annual “See C. diff” awareness-raising campaign, attendees gave our first-ever Scientific Symposium a rating of 96% in 2024.
4,000
PLF has the largest network of C. diff patients, survivors and caregivers, including our volunteers, who engage in peer support, advocacy, and public speaking.
9
PLF has convened nine National C. diff Summits and six Lobby Days. In addition to empowering volunteers and educating the public, these have resulted in greater funding for public health and language requesting increased surveillance for C. diff in the 2023 Federal Budget.
2,122
More than 2,000 Americans have signed our petition to the Centers for Disease Control & Prevention to designate C. diff as a Nationally Notifiable Disease.
60
PLF has trained more than 60 C. diff survivors and caregivers to serve as members of our Advocates Council. Our Advocates engage in lobbying, peer support, awareness raising, and media outreach.
1,056
More than 1,000 people have downloaded our C. diff Care and Lifestyle & Nutrition Guides.
$2.2 Million
PLF has raised more than $2.2 Million for C. diff awareness and advocacy.
1st
Conducted the inaugural FDA C. diff patient listening session.
194
194 C. diff survivors or caregivers have shared their story with PLF.
