Driving research of Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS),
Post Treatment Lyme Disease Syndrome (PTLDS), Fibromyalgia and Post COVID .

News

Special Request! Join OMFCA’s Hope Builders Community

Introducing April: An artist, person with ME/CFS, & OMF Hope Builder.

Read More →

Out Now! Itaconate Shunt Hypothesis Part 2 – Video Interview with Robert Phair & Janet Dafoe

Discover the latest advancements in ME/CFS research with the second installment of the Itaconate Shunt Hypothesis video, with Robert Phair PhD and Janet Dafoe, PhD

Read More →

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

Highlights and progress: OMFCA’s 2022 Year in Review

Read More →

LAST DAY in 2022 to donate!

Only a few hours left in 2022 to help OMF fund small treatment trials!

Read More →

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.

Read More →

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!

Read More →

“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.

Read More →

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.

Read More →

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

Read More →