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.
Does ME/CFS Have a Biomolecular Signature? An OMF Supported Study Aims to Find out…
An OMF supported study led by Alain Moreau, PhD at the Montreal Collaborative Research Center aims to find out.
The Crisis of Sick Children with Long COVID and ME/CFS: We Need Your Help to Fund Research!
Many of the #millionsmissing with ME/CFS and Long COVID include children. Once healthy and energetic adolescents, their lives have now been put on pause.
TRIPLE your impact to help us find an effective treatment! #TripleGivingTuesday begins today!
From November 1 through November 29 2022, all donations to OMFCA are TRIPLED up to a total of $500,000!
