Denmark
Research[edit | edit source]
- 2015, The Health-Related Quality of Life for Patients with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS)[1] - (Full text)
Researchers[edit | edit source]
- Henrik Nielsen
- Ivan Brandslund
- Per Fink (psychological paradigm proponent)
- Rikke Olsen
- Louise Brinth
- Jesper Mehlsen
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]
Fast forward to 2024, and nothing has happened. Denmark still uses a psychosocial model. Per Fink has had the final say on ME/CFS in Denmark since 2007.
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]
- ↑ 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.
- ↑ 2.0 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.
- ↑ "Tv fra Folketinget". Folketinget (in dansk). Retrieved February 26, 2021.
