Looking Back and Looking Forward: OMFCA’s 2022 Year in Review

Highlights and progress: OMFCA’s 2022 Year in Review
LAST DAY in 2022 to donate!

Only a few hours left in 2022 to help OMF fund small treatment trials!
ONE DAY left to make your 2022 donation!

Only ONE more day to make your 2022 donation to OMF and help fund small treatment trials.
LAST DAY this year to TRIPLE your impact toward treatment trials!

Support small ME/CFS treatment trials: Nov. 29, 2022 is the LAST DAY this year to get your donation to OMF TRIPLED!
“How my love for Star Wars led to research into the disease that ruined my life.”

How does OMF research give hope? In a viral Redditt post, an ME/CFS patient known to OMF shares the unique story of how their love of Star Wars inspired hope and led to OMF-supported research.
Ron Davis: New Neutrophil Study!

A new study from Ron Davis and Stanford colleagues aims to identify neutrophil abnormalities that are unique to ME/CFS patients.
Our Community Comes Together This Giving November

OMF highlights stories of those who raise awareness and further our mission to end ME/CFS, Long COVID, and related diseases
Jacqueline Ko, Exclusive Interview!

As part of Triple Giving Tuesday, we are so excited to be joined by OMF Ambassador Jacqueline Ko for an exclusive new video interview.
Post Exertion Malaise (PEM): David Systrom aims to fill in gaps

CPET testing clearly shows the effects of exertion intolerance (PEM) in ME/CFS. Learn more about David Systrom’s study.
Does ME/CFS change molecularly throughout a day? Bergquist and Armstrong’s new study

This study plans to use high frequency blood testing to evaluate what changes in ME/CFS patients over the course of a day.