ME/cvs Vereniging

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Revision as of 14:17, September 23, 2019 by Notjusttired (talk | contribs) (→‎Patient survey: restore info from patient survey that should not have been deleted, clarify wording)
Logo of the Dutch ME/CFS Association

The ME/cvs Vereniging is a Dutch association for and by those suffering from ME/CFS and their close ones. The small letters for "CVS" in its name underpins that the association wishes the medical world to stop using the name Chronic Fatigue Syndrome, which it considers stigmatizing. ("CVS" is the Dutch abbreviation for Chronic Fatigue Syndrome.)

Aims[edit | edit source]

The association's objective is:

  • To provide and disseminate information about myalgic encephalomyelitis (code G93.3 in the ICD-10)
  • To provide and disseminate information about chronic fatigue syndrome (code G93.3 in the ICD-10)
  • promote the best possible outcomes for people suffering from ME/CFS, their partners, relatives and others close to them
  • promote a clear public image of ME/CFS
  • encourage those suffering from ME/CFS, their partners, relatives and those close to them in activities aimed at improving or restoring their health and improving their living conditions[1]

History[edit | edit source]

ME/cvs Vereniging, originally known as ME en CVS Vereniging, was founded on April 15, 2005[1] by Eelco van Tuyll, Rico Landman and Guido den Broeder.[2] In 2011, Guido den Broeder left as chairman and founded ME Vereniging Nederlands.[3][4]

Funding[edit | edit source]

Their funding comes from individual contributions and donations.[citation needed]

Patient survey[edit | edit source]

In 2019, the association released a report summarizing the results of a 2017 patient survey.[5] This report only included responses from patients who met the SEID diagnostic criteria, as these diagnostic criteria were considered consistent with the recent report by the Gezondheidsraad (Dutch Health Council).[5] Of those completing the survey, 94% reported a diagnosis of ME, 2.6% reported a diagnosis of CFS, no patients reported a diagnosis of SEID, and 4% reported a different diagnosis.[5](p15)

Online presence[edit | edit source]

Learn more[edit | edit source]

References[edit | edit source]

  1. 1.0 1.1 ME/cvs Vereniging (October 17, 2012). "Statuten". www.me-cvsvereniging.nl (in Nederlands). Cite has empty unknown parameter: |dead-url= (help)
  2. ME/CVS Vereniging. "ME/CVS Vereniging" (in Nederlands). Archived from the original on July 16, 2011. Unknown parameter |dead-url= ignored (|url-status= suggested) (help)
  3. ME/cvs Vereniging (October 2011). "Algemene Ledenvergadering". Archived from the original on October 2, 2011. Retrieved September 23, 2019. Unknown parameter |dead-url= ignored (|url-status= suggested) (help)
  4. ME Vereniging Nederland. "ME Vereniging". mevereniging (in Nederlands). Retrieved September 23, 2019. Cite has empty unknown parameter: |dead-url= (help)
  5. 5.0 5.1 5.2 Corsius, L.; Crijnen, B.; Hogeweg; Kuijper (September 2019). "Zorg voor betere behandeling bij ME" (PDF). ME/cvs Vereniging. Retrieved September 11, 2019. Cite has empty unknown parameter: |dead-url= (help)