Triple Giving November is Here: Your Gift Goes 3x Further!

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 to our generous matching donors. This represents a crucial opportunity to accelerate ME/CFS and Long […]
Recognizing POTS Awareness Day: Join Us in Spreading Awareness!

Recognizing POTS Awareness Day: Join Us in Spreading Awareness! October is Dysautonomia Awareness Month, and today, October 25th, we recognize POTS Awareness Day! At OMF Canada, we stand united with millions worldwide to amplify awareness of these often-overlooked conditions. Living with POTS can make doing even the simplest of tasks feel incredibly difficult. I never […]
Preprint: A Network Medicine Approach to Investigating ME/CFS Pathogenesis in Severely Ill Patients: A Pilot Study

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 network medicine approach, the team created a SIPS disease module that showed strong interplay with […]
New Study from the ME/CFS Collaborative Center at Uppsala: Altered Metabolic Pathways in ME/CFS

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. Untargeted and targeted analysis of metabolites revealed significant changes in metabolic networks of ME/CFS patients […]
Life Improvement Trial (LIFT) has officially begun!

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 and screening began in August and the first participants have now been enrolled. What is […]
Watch Now: Recordings from the Portugal ME/CFS and Long COVID Conference!

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 share and discuss the latest biomedical evidence and findings on ME/CFS and the nexus between […]
Celebrating a Milestone: StudyME Registry Surpasses 10,000 Participants!

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 proudly launched OMF StudyME, a participant registry powered by StudyPages. This innovative recruitment […]
Insights into Severe ME/CFS: Honoring Severe ME/CFS Awareness Day

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 one of heart-wrenching challenges and remarkable courage. Since 2004, this disease has tested his limits, […]
Celebrating 2 Years of MERC: Transforming Medical Education for ME/CFS and Long COVID

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 Bateman Horne Center, supported by Open Medicine Foundation (OMF). Here is a snapshot of […]
Join Theresa in Building Hope for ME/CFS Research!

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 university, a career, and a family life were dramatically altered. Yet, her unwavering spirit and […]