From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history

Research[edit | edit source]

Researchers[edit | edit source]

Medical guidelines[edit | edit source]

National health department[edit | edit source]

In 2019, the Danish parliament unanimously voted to separate ME/CFS from functional disorders (medically unexplained symptoms), and to treat the disease as a physical neurological illness using the World Health Organization classification rather than as psychosomatic illness, and called upon the department of health to update it's information.[2][3]

In previous years, the controversial biopsychosocial model was the main approach to treatment for patients with ME/CFS in Denmark.[2]

CBT/GET[edit | edit source]

Social security and disability benefits[edit | edit source]

Access to care[edit | edit source]

How many hospitals&doctors, which diagnose and treat ME (estimate): Rehabilitation offers for ME sufferers:

Notable patients[edit | edit source]

Links[edit | edit source]

See also[edit | edit source]

References[edit | edit source]

  1. Falk Hvidberg, Michael; Brinth, Louise Schouborg; Olesen, Anne V.; Petersen, Karin D.; Ehlers, Lars (July 6, 2015). Furlan, Roberto (ed.). "The Health-Related Quality of Life for Patients with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS)". PLOS ONE. 10 (7): e0132421. doi:10.1371/journal.pone.0132421. ISSN 1932-6203.
  2. 2.0 2.1 Invest in ME Research (March 1, 2019). "There is something right in the state of Denmark". Invest in ME Research. Retrieved February 26, 2021.
  3. "Tv fra Folketinget". Folketinget (in dansk). Retrieved February 26, 2021.