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Join date: Jan 28, 2018
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This profile is the official Society Admin.
The MEFM Society of BC is a small patient-run not for profit society that was formed to help and support people living with the health conditions of Myalgic Encephalomyelitis * (ME) and/or Fibromyalgia (FM) and their families.
We help people in BC and elsewhere understand their illnesses and seek and obtain appropriate medical help and treatments to improve their health and quality of life.
Posts (58)
Mar 26, 2026 ∙ 3 min
Long COVID: Why Clarity Matters More Than Ever
Recently, our Society was involved in reviewing a Long COVID research protocol. There were several concerns. But one stood out. The study largely treated Long COVID as a single illness, with a single protocol design for all participants, implicitly assuming that all Long COVID patients have similar symptoms, risks, and responses to treatment. That assumption is the problem. Because what we call “Long COVID” is not one condition. It is a catch-all term for a few very different long-term...
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Mar 3, 2026 ∙ 1 min
Solve M.E. Research Announcement
Two upcoming research projects, Effect of Semaglutide on ME/CFS Symptoms and Discovery of Target Antigens for Dysfunctional T Cells in ME/CFS and Long COVID , bring hope for improved diagnosis and targeted treatments. Read more about these projects here .
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Mar 3, 2026 ∙ 1 min
Science Is Finally Validating Your Reality
The information below was initially shared on January 9, 2026. In November, researchers at the University of East Anglia announced a blood test that diagnoses ME/CFS with 96% accuracy . Let that sink in! For years, many of you have been told your illness is "all in your head." This test proves what you already knew: ME/CFS has a clear biological signature. It's measurable. It's real. "For the first time, we have a simple blood test that can reliably identify ME/CFS — potentially...
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