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  1. The ME Association has been providing expert help since 1980. We understand the challenges faced by people with ME/CFS and Long Covid and believe that nobody should struggle alone. We provide a safe and welcoming community for people to come together and benefit from sharing their experiences.

    • Support

      The ME Association works with local support groups to...

    • Me Association Shop

      Members receive the excellent, ME Essential Magazine, for a...

    • About The Me Association

      understand the challenges faced by people with PVFS, ME/CFS,...

    • Membership

      Membership is available to any adult with ME/CFS or Long...

  2. The ME Association provides expert help, support, information, and research for people with post-viral fatigue syndrome, myalgic encephalomyelitis, and long Covid. Learn about their services, campaigns, and community.

  3. ME Association. 32,416 likes · 1,064 talking about this · 35 were here. We help to make the UK a better place for people with ME/CFS, PVFS, and Long Covid.

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  4. Myalgic encephalomyelitis, also called chronic fatigue syndrome or ME/CFS, is a long-term condition that can affect different parts of the body. The most common symptom is extreme tiredness. The cause of ME/CFS is unknown. ME/CFS can affect anyone, including children.

  5. The 25% M.E. Group is a UK-based charity that campaigns for awareness and support of people with severe M.E. (Myalgic Encephalomyelitis). Learn more about M.E., join, donate, fundraise or get involved in their activities.

  6. A charity investing in ME research. ME Research UK is a charity with the primary aim of funding high-quality biomedical research into the causes, consequences and….

  7. ME/CFS is a chronic illness with symptoms such as fatigue, pain, cognitive problems and post-exertional malaise. Learn about the diagnosis, causes, treatments and research into ME/CFS from ME Research UK, a charity funding biomedical research.

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