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ME Foreningen
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
ME Foreningen is a patient group for those who have myalgic encephalomyelitis in Denmark.[1] ME Foreningen should not be confused with the similarly named Swedish patient group ME-föreningen.
Aims[edit | edit source]
Services[edit | edit source]
ME Foreningen is a member of EUROMENE, the European ME Alliance.[2]
Notable people[edit | edit source]
Patrons[edit | edit source]
Medical advisors[edit | edit source]
Research/Notable studies[edit | edit source]
- 2015, The Health-Related Quality of Life for Patients with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS)[3] - (Full Text)
History[edit | edit source]
Funding[edit | edit source]
Interviews and articles[edit | edit source]
Online presence[edit | edit source]
- ME Foreningen Website
- Unrest DK Facebook group
- YouTube channel
- Email mail@me-foreningen.dk
- Telephone: [95 97 00|44 95 97 00]
- Admin: Wednesday and Friday 14.00 – 16.00
- Patient support:
Wednesday and Friday 12.00 – 14.00
See also[edit | edit source]
- ME-föreningen - Swedish charity
Learn more[edit | edit source]
References[edit | edit source]
- ↑ "ME Foreningen". me-foreningen.dk. Retrieved June 21, 2022.
- ↑ European ME Alliance. "European ME Alliance Group members". European ME Alliance. Retrieved September 18, 2019.
- ↑ Hvidberg, Michael Falk; Brinth, Louise Schouborg; Olesen, Anne V; Petersen, Karin D; Ehlers, Lars (July 6, 2015). "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.
