Message from Anna: Finding Hope in Community!
Dear OMF Community, My name is Anna Carina, and I live with my family in Vaxholm, Sweden. In 2016, our son Lucas fell ill with ME/CFS after having a glandular fever at the age of 13. We went through the
Dear OMF Community, My name is Anna Carina, and I live with my family in Vaxholm, Sweden. In 2016, our son Lucas fell ill with ME/CFS after having a glandular fever at the age of 13. We went through the
Today, we are excited to share a new publication from Christopher Armstrong, PhD, and colleagues: “Unravelling shared mechanisms: insights from recent ME/CFS research to illuminate long COVID pathologies.” This comprehensive review is proudly supported by OMF. From the Desk of Christopher Armstrong,
Step into spring as a Hope Builder! With the arrival of a season that symbolizes renewal and progress, we at Open Medicine Foundation are inspired by the strength of those living with ME/CFS and Long COVID. This season of new
Today, we unite in solidarity to observe Long COVID Awareness Day. This day holds profound significance for countless individuals worldwide. We stand together in spirit and purpose, recognizing the extensive impact of SARS-CoV-2. This day serves as a beacon in our
I am thrilled to announce that Danielle Meadows, Ph.D., has joined Open Medicine Foundation as our new Vice President of Research Programs & Operations. With her exceptional background and expertise in biomedical engineering, research administration, and project management, Danielle is poised to play
Imagine our collective strength when we unite for a cure. At Open Medicine Foundation (OMF), we are driven to find effective treatments for ME/CFS and Long COVID. Our global collaboration model harnesses the brightest minds to bring relief to you and
Join the Momentum! Finding people with ME/CFS and Long COVID who can participate in studies is one of the biggest barriers to research. You could be the solution! We’re delighted to share that the OMF StudyME Registry has reached a pivotal achievement
Today, we are privileged to bring you the narrative of extraordinary courage, resilience, and strength. At just 14 years old, Charlotte’s life took an unexpected turn with a diagnosis of ME/CFS. Read Charlotte’s story in her own words:
The ME/CFS Research Roadmap webinars, hosted by the National Institute of Health (NIH), have successfully concluded. These virtual events brought together ME/CFS experts to present current research, identify knowledge gaps, and explore future research opportunities for ME/CFS. Open Medicine
We are excited to share a new publication from the research funded by Open Medicine Foundation (OMF). Jonas Bergquist, MD, PhD, OMF Chief Medical Officer and Director of the OMF-supported ME/CFS Collaborative Research Center at Uppsala University, and colleagues, have
As 2024 begins, we at Open Medicine Foundation are thrilled to review a few highlights and the milestones you made possible in 2023. It was a year filled with incredible achievements, groundbreaking research, and community empowerment. Thanks to your unwavering support, we’ve reached new
Open Medicine Foundation is thrilled to share a new publication from Alain Moreau, PhD & colleagues: “Exploring the neurocognitive consequences of post-exertional malaise in myalgic encephalomyelitis.” This study shows the impact of post-exertional malaise (PEM) on the disturbance of cognition
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