Call for 6 participants to be interviewed related to a British Columbia ME community engagement project

We are pleased to announce that the ME|FM Society of BC, in partnership with the Complex Chronic Diseases Program (CCDP) at BC Women’s

In their efforts to bring desperately needed resources and world-class research to the fight against ME, Open Medicine Foundation (OMF) has established Open ...

At a press conference last month, Federal Minister for Health, Ginette Petitpas Taylor, announced Canadian Institutes of Health Research (CIHR) funding for M...

Thanks to #MEAction and Jaime Sel for keeping us updated on the latest in ME research! For the full summary, go to their SEPT & OCT - RESEARCH ROUNDUP

Thanks to Dr. Charles Shepherd and ME Association (UK) for producing their 13 page summary report on the 2018 Invest in ME Research Conference. Read the ME A...

ME Research UK has just published an article reporting on a newly funded study by Prof. Jarred Younger, University of Alabama. "The central hypothesis ... is...

Watch this new research video update by OMF’s Scientific Advisory Board member, Mark M. Davis, PhD, produced by Ashley Haugen for this #OMFScienceWednesday....

Thanks to Cort Johnson for his excellent reporting, published on the Simmaron Research blog, of the exciting new research presented at the 1st Canadian Colla...

AFTER UNREST is a short documentary about Myalgic Encephalomyelitis (also known as ME/CFS or chronic fatigue syndrome) created by Australian ME patient, Ketr...

ME Research Highlights Stanford Community Symposium The Open Medicine Foundation (OMF) sponsored a Community Symposium on the Molecular Basis of ME/CFS at St...

Our Society joined patients and patient in a meeting with the CIHR's new Director, Institute Muskuloskelatal Health and Athritis, Dr. Karim Khan, to discuss ...

At our October 30 screening of Unrest with UBC Medical and Nursing students, we surveyed them on their knowledge and experience with ME/CFS. Here are the sur...

It's been quite a few years now that I (Kati) have discovered that if I, and we as a patient population, didn't get to work on advocacy and about how we want...

By Howard Searle Have you ever wondered what research is being done here in BC into the mystery of Myalgic Encephalomyelitis? I had this very thought, so I c...

My name is Daisy Sanchez-Ziller, I’m a 24-year old soon-to-be nursing student from Vancouver. My sister, Jasmine, has been sick with Myalgic Encephalomyeliti...