The Post Exposure Foundation
A place to learn
A place to make an actionable plan
A place where you are believed and heard
Our Mission
Our mission is to ensure that no sufferer of any post exposure syndrome goes unrecognized and unheard
We do this by organizing evidence, gathering data, providing resources, providing advocacy services, and most importantly– making noise.
Our goal is to empower patients in order to push establishment medicine to catch up with the reality patients are already living.
What We Do
-
The official PSSD/PFS/PAS database.
It's easy to underestimate the power for data. At PEF, we're building a detailed database of interventions for post-exposure syndromes – to be released publicly on Kaggle for open analysis. That way, it not only increases awareness but also allows for groundbreaking insights to be found. Its precision– not only if something works, but for who.
Interested in participating? Click here
-
Many living with post-exposure disorders are too symptomatic to advocate for themselves — or too exhausted from years of dismissal by conventional medicine. You shouldn't have to keep fighting alone to be believed.
That's where we come in. We have an international directory of clinics and physicians who understand what you are experiencing
-
A centralized library built for patients navigating post-exposure conditions.
Includes peer-reviewed research, curated articles, anecdotal recovery reports from real patients, and a directory of physicians and clinics with experience treating these conditions — all in one place
Our database includes
International clinics, physicians and hospitals that work with post exposure syndromes (PES)
Clinical trials, and research papers
Anecdotal reports of recovery
A unified list of PES resources, platforms, and forums
Learn More About The Conditions We Serve
