ME (cfs) Awareness

Your help is needed to email or copy and distribute the leaflet below, to encourage action which will result in better health outcomes for people with ME (cfs). Thank you.

What if you, or someone close to you, fell ill with Myalgic Encephalomyelitis (cfs) and:

  • you can’t get promptly diagnosed?
  • you can’t find a ME (cfs) doctor or specialist?
  • you can’t receive medical treatments based on latest studies and research?

Teenagers, and people of all ages, may be bedridden or incapacitated for months, or years, impacting their relationships, education, employment, retirement, independence and quality of life.

Help stop the suffering. Talk to medical specialists,

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politicians, and scientists, about treatments and funding for research, clinical trials, and the establishment of specialist ME (cfs) clinics.

Some of the latest research and developments can be accessed at:

Search for the pioneering and latest work of Prof Kenny De Meirleir.

For clinical studies and a treatment option for a subset of patients, go to:

Print ME/CFS Awareness (PDF, 14Kb)