Groundbreaking Awareness and Fundraising: Physics Girl Livestream’s Incredible Results

We are overflowing with gratitude and hope following the incredible live-streaming event hosted by Dianna Cowern (Physics Girl) and her outstanding team. Your engagement and generosity have shattered our expectations. What started as a goal to raise $10,000 turned into a mind-blowing $121,983 fundraiser and still growing! Missed the Live Event? Watch It Now! Dianna’s […]
Join Physics Girl’s Livestream: A Day in the Life with Long COVID and ME/CFS

If you are a science enthusiast, you have probably heard of Dianna Cowern, an American science communicator and YouTuber known as Physics Girl, who is living with Long COVID and ME/CFS. This Saturday (July 6, 2024), Dianna’s team will be live-streaming a day in her life, showcasing what it’s like for her to suffer from […]
Systems Modeling Reveals Shared Metabolic Dysregulation and Novel Therapeutic Treatments in ME/CFS and Long COVID

The Heart of the Matter In a recently released preprint, OMF’s computation team investigated the shared metabolic symptoms found in ME/CFS and Long COVID. Using new modeling technology, the team identified metabolic pathways that are dysregulated in both ME/CFS and Long COVID. They identified a combination of L-ornithine and L-aspartate (LOLA) as a potential treatment […]
Major Milestone: Australian Government Funds Update of ME/CFS & Long COVID Clinical Guidelines

We are thrilled to announce that, as a direct outcome of the Canberra Roundtable convened in late March and led by Emerge Australia with the support of Open Medicine Foundation Australia, the Australian government has committed funding to update the clinical guidelines for ME/CFS and Long COVID. The current clinical guidelines for ME/CFS are over […]
Personalized Treatment Trials: Video Update!

The Heart of the Matter General practitioners (GPs) often trial different treatments with their ME/CFS and Long COVID patients. In partnership with GPs, by studying the outcomes of each treatment, the patient’s lived experience, and the personal history of the patient, the Personalized Treatment Trials project is looking to understand why someone may or may not […]
Watch Now: Fran Haddock’s Candid Interview on ME/CFS!

Today, we are excited to share an exclusive video interview featuring Fran Haddock, a dedicated advocate for ME/CFS, chronic illness, environmental, and social justice causes. Fran’s profound six-year journey with ME/CFS took a significant turn after a COVID-19 infection, escalating her symptoms to severe. In this candid conversation, Fran shares her path, unveiling the intricate […]
Unlocking New Insights: Food and Saline Infusions in ME/CFS Research

The Heart of the Matter Food and saline infusions are both known to have an impact on ME/CFS symptoms. The Melbourne ME/CFS Collaboration is aiming to identify responses to different foods using objective measures, which may also prove useful in future trials. The team will also try to understand the impact of saline infusions to […]
Join Kim and Andrew in Transforming ME/CFS Awareness

Today, we’re thrilled to showcase the impactful work of Kim Eggers and Andrew Gifford, OMFCA supporters whose unwavering dedication to amplifying awareness and understanding of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is truly inspiring. Meet Kim Eggers Kim Eggers has had ME for 34 years, and as such, is passionate about the mysteries of the disease […]
Watch Now! New Research Update from the Melbourne ME/CFS Collaboration

The Heart of the Matter Hormones impact the immune system and energy metabolism, which are both considered major parts of the biological cause of ME/CFS. Changes in hormone levels may impact the development of the disease and its severity. The MELLOW project aims to measure fluctuations in hormones across the menstrual cycle, […]
Join Us in Accelerating Hope

Every May, Open Medicine Foundation Canada (OMFCA) unites with supporters worldwide to mark International ME/CFS Awareness Day on May 12 through our annual May Momentum campaign. This pivotal time allows us to spotlight the profound challenges faced by those living with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and to raise vital funds needed to propel OMFCA […]