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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. The ME Association offers phone helpline, local support groups, NHS services and other resources for people with M.E. (myalgic encephalomyelitis) or Long COVID. Find out how to access confidential and reliable information and advice.

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  4. ME Association. 32,421 likes · 1,320 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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  5. 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.

  6. 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.

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  8. 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….

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