European ME Alliance

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The European ME Alliance is a group of European patient groups for myalgic encephalomyelitis (ME or ME/CFS).[1] It was formed in 2008 and set up to lobby for increased funding for biomedical research to lead to for patients. It now has representatives from Belgium, Denmark, Germany, Holland, Ireland, Italy, Norway, Spain, Sweden, Switzerland and the UK.

Member organisations

Online presence

References

  1. "EMEA". www.euro-me.org. Retrieved September 6, 2019.
  2. "European ME Alliance - EMEA Holland". www.euro-me.org. Retrieved September 18, 2019.
  3. European ME Alliance. "European ME Alliance Group members". www.euro-me.org. Retrieved September 18, 2019.

The information provided at this site is not intended to diagnose or treat any illness.
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history.