At Open Medicine Foundation (OMF), we are dedicated to pioneering innovative treatments and medical education for ME/CFS and Long COVID. But we can’t do it alone—we need partners who believe in lasting change. That’s where Hope Builders come in. Hope
We are reaching out to invite those of you who would like to participate in research studies to join StudyME, a free global participant registry proudly launched by Open Medicine Foundation (OMF) in April 2023. This innovative recruitment tool is
Types of Outcome Measures From the Desk of Dr. Danielle Meadows, Vice President of Research Programs & Operations In an effort to talk a little more about the nuances of the research process, last month I honed in on an
Last year, Open Medicine Foundation (OMF) featured Rachel Riggs and her cookbook, In Good Health: Uncomplicated, Allergen-Aware Recipes for a Nourished Life, in an exclusive interview. The book is now available for pre-order, and Rachel has pledged to donate the
At Open Medicine Foundation (OMF), we’re constantly exploring innovative ways to advance ME/CFS and Long COVID research. Today, we want to introduce several unique ways you can support our mission. Shop Online and Support OMF at No Extra Cost Your
Big Data and Artificial Intelligence (AI) have great potential to advance precision medicine for ME/CFS and Long COVID. Dr. Chris Armstrong and his colleagues have recently published a paper titled “Machine learning and multi-omics in precision medicine for ME/CFS”. In
As we step into 2025, we reflect on the remarkable progress made in 2024. We’re deeply grateful for the support you’ve shown. Thanks to you, our community, we’ve made significant strides in advancing the understanding and treatment of ME/CFS and
Open Medicine Foundation (OMF) is proud to announce the addition of two distinguished experts to our esteemed Scientific Advisory Board (SAB): Dr. Michelle James and Dr. David Kaufman. Their appointments underscore OMF’s commitment to driving progress in ME/CFS and Long
The underlying biological mechanisms for ME/CFS remain unclear and have rarely been investigated in the adolescent population, despite this period representing an age peak in the overall incidence. We’re pleased to share the ‘Serial Pediatrics Omics Tracking in Myalgic Encephalomyelitis
What Is a “Well-Powered” Study? From the Desk of Dr. Danielle Meadows There are many nuances that contribute to the complexity and duration of the research process I introduced back in October, 2024. Therefore, I wanted to take time each
Time is running out! With just a couple of hours in 2024 left, your year-end gift can help launch groundbreaking research initiatives in 2025. Our scientists are poised to build on this year’s momentum—will you help drive their work forward?
As 2024 draws to a close, we want to take a moment to reflect on the progress we’ve made together. Your support—whether through donations, fundraising, or sharing our mission—has been invaluable in our quest to understand and conquer ME/CFS and
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