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The ME Association supports people with ME/CFS through all stages of their illness.

The ME Association is a national charity that supports thousands of people with ME/CFS each year in the UK. ME/CFS is a neurological disease affecting adults and children from all ethnic backgrounds.

Between 130,000 and 260,000 people in the UK are struggling to live with this debilitating condition. At least 25% of them will be housebound or bedbound. It can affect people for many years, even decades, and lead to long-term disability and a poorer quality of life than multiple sclerosis or cancer.

We provide information and support for patients, families and carers who are affected by Myalgic Encephalopathy/Encephalomyelitis, Chronic Fatigue Syndrome (ME/CFS), Post-Viral Fatigue Syndrome (PVFS), and Long Covid.  

We campaign to raise awareness of the inequalities affecting the patient community and we aim to achieve recognition and fair treatment for all.

We fund and support vital biomedical research and offer education and training for healthcare professionals who want to learn more about this often-misunderstood medical condition. 

The ME Association: We’re here for you! 

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