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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!
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“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 ...
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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.
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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
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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.
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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.
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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.
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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.
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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.
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