Help us make a difference for severe M.E. sufferers

The 25% M.E. Group is a nationwide charity. We campaign to raise awareness of M.E and provide services to people affected by severe M.E. (Myalgic Encephalomyelitis). Your support is vital to our success. Join us to become a member, donate or get involved in our campaigning.

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Severe M.E

Suffering from Severe M.E.? What to know how it affects people? Want to know current developments and how we can help? Learn More today.

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Join us today in helping severe M.E. sufferers. Your donations and memberships subscriptions help us do this.

Fundrasing

Want to help raise funds to support severe M.E.? or have any suggestions visit our fundraising page.

Campaigning

Get Involved! You can help us campaign and help raise awareness for severe M.E. Sufferers.

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Latest News

Back to the Future? Immunoglobulin Therapy for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

Simon Lawrence 12/11/2021

The findings of controlled trials on use of intravenous immunoglobulin G (IV IgG) to treat myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) are generally viewed as representing mixed results. On detailed review,…

NICE ME/CFS Guideline 2021 (BMJ

Simon Lawrence 29/10/2021

ME/CFS: Exercise goals should be set by patients and not driven by treatment plan, says NICE NICE ME.CFS Guideline 2021 (BMJ

Expert reaction to updated NICE guideline on diagnosis and management of ME/CFS

Simon Lawrence 29/10/2021

The National Institute for Health and Care Excellence (NICE) has published its updated guideline on the diagnosis and management of myalgic encephalomyelitis (or encephalopathy)/chronic fatigue syndrome (ME/CFS). https://www.sciencemediacentre.org/expert-reaction-to-updated-nice-guideline-on-diagnosis-and-management-of-me-cfs/