May 12 is ME/CFS Awareness Day. Fuel progress all month long—join the May Momentum campaign!
As part of our Triple Giving November campaign, we are excited to share an interview with David Systrom, MD, discussing a muscle biopsy study aimed at understanding the molecular mechanisms behind Post-Exertional Malaise (PEM). Triple My Gift A Muscle Biopsy Study to Understand
Triple Giving November has officially begun! We’re excited to kick off our biggest fundraising event of the year – Triple Giving November! From November 1 to December 3, every donation to OMF will be TRIPLED, up to $500,000, thanks
Open Medicine Foundation’s Research Programs Open Medicine Foundation (OMF) is dedicated to conducting research focused on finding effective treatments and diagnostic markers for ME/CFS and Long COVID. As part of this pursuit, OMF collaborating centers have over 35 projects that
Recognizing POTS Awareness Day: Join Us in Spreading Awareness! October is Dysautonomia Awareness Month, and today, October 25th, we recognize POTS Awareness Day! At Open Medicine Foundation, we stand united with millions worldwide to amplify awareness of these often-overlooked conditions.
The Heart of the Matter OMF’s Computational Research Center and the ME/CFS Collaborative Center at Stanford University have released a preprint of their work investigating the pathogenesis of ME/CFS using data from the severely ill patient study (SIPS). Using a
The Heart of the Matter The ME/CFS Collaborative Center at Uppsala published an article on altered metabolic pathways in ME/CFS. The tryptophan metabolic pathway is highly relevant to ME/CFS because of its roles in immune function, neurotransmission, and energy metabolism.
The Life Improvement Trial (LIFT) has officially begun! Conducting a proper clinical trial and ensuring all logistics are set up takes time, so we are excited to share that Open Medicine Foundation’s Life Improvement Trial (LIFT) has officially launched. Recruitment
We are pleased to share that recordings from the 1st International Conference on Clinical and Scientific Advances in ME/CFS and Long COVID are now available! This event, the first in Portugal, brought together leading scientists, clinicians, and international experts to
Join us in making a difference: Sign up today and be a part of the solution! Let’s celebrate! We are thrilled to share a monumental milestone with you: OMF StudyME Registry has now surpassed 10,000 participants! In April 2023, we
Today, August 8, we unite to honor Severe ME/CFS Awareness Day. This year, we raise awareness through the lens of Whitney Dafoe. Whitney, son of Ron Davis, PhD, and Janet Dafoe, PhD, is an extraordinary soul whose ME/CFS journey has been
In 2022, we set out to educate healthcare professionals about diagnosing and managing ME/CFS and other chronic complex diseases. Today, we are thrilled to celebrate the successful completion of the second year of the Medical Education Resource Center (MERC) at
Imagine a life where your everyday dreams suddenly become a distant memory. For Erica, a vibrant young adult diagnosed with ME/CFS at just 14, the journey has been a relentless battle against fatigue, migraines, and cognitive dysfunction. Her aspirations for
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