Wikisage, the free encyclopedia of the second generation and digital heritage, wishes you merry holidays and a happy new year!
ME/CVS Vereniging: Difference between revisions
(start) |
(minus superfluous refs (films are linked to at hyves)) |
||
Line 22: | Line 22: | ||
==Educational Films== | ==Educational Films== | ||
In 2006 the ME/CVS Vereniging asked students from the [[Hogeschool Rotterdam]] to make an educational film on ME/CFS. The film features medical expert Dr. Ruud Vermeulen ([[CVS Research Centrum]], [[Amsterdam]]) and patients Christine van Reeuwijk and Arno Hogendoorn. | In 2006 the ME/CVS Vereniging asked students from the [[Hogeschool Rotterdam]] to make an educational film on ME/CFS. The film features medical expert Dr. Ruud Vermeulen ([[CVS Research Centrum]], [[Amsterdam]]) and patients Christine van Reeuwijk and Arno Hogendoorn. On [[Youtube]] the film has the highest possible rating. A new group of students made a second film for the ME/CVS Vereniging in 2008. Both films can be found at the association's hyve. | ||
==Books by members== | ==Books by members== | ||
Line 31: | Line 31: | ||
* [http://www.me-cvsvereniging.nl/ ME/CVS Vereniging] | * [http://www.me-cvsvereniging.nl/ ME/CVS Vereniging] | ||
* [http://me-cvs-vereniging.hyves.nl/ ME/CVS Vereniging on Hyves] | * [http://me-cvs-vereniging.hyves.nl/ ME/CVS Vereniging on Hyves] | ||
* [http://www.me-cvs-stichting.nl/ ME/CVS Stichting Nederland] (''ME/CFS Foundation'') | * [http://www.me-cvs-stichting.nl/ ME/CVS Stichting Nederland] (''ME/CFS Foundation'') | ||
* [http://www.steungroep.nl/ Stichting Steungroep ME en Arbeidsongeschiktheid] (''Support Group for ME and Disability'') | * [http://www.steungroep.nl/ Stichting Steungroep ME en Arbeidsongeschiktheid] (''Support Group for ME and Disability'') |
Revision as of 19:20, 4 August 2008
The ME/CVS Vereniging (ME/CFS Association) is the patient association for myalgic encephalomyelitis / chronic fatigue syndrome in the Netherlands.[1]
Goals
The association aims to advocate the interests of all patients and their kin in the widest sense of the word. Priority in the policy plan for 2006-2008 is to provide information, since according to the association there is a serious lack of knowledge about ME/CFS in the Netherlands.[2] The association also aims to combat prejudice and discrimination[3][4][5] and to foster patient contact. In addition, the association stimulates, reviews[6] and supervises[7] scientific research, and together with other patient organizations represents patients in the development of protocols and guidelines.[8] The ME/CVS Vereniging publishes the magazine Lees ME[9] (Read ME), as well as leaflets, brochures, an electronic newsletter, etc.
History
In 2003, the ME Stichting (ME Foundation, now ME/CVS Stichting Nederland), founded in 1987, was advised to transform into a democratic organization. According to an independent bureau, it did not properly look after the interests of the patients.[10] A number of patients concluded that the advice had been ignored and started the ME/CVS Vereniging on April 15, 2005.[11] Three years later, the association had 300 members.
Role in ME/CFS guidance in the Netherlands
A research project supervised by the ME/CVS Vereniging suggested poor knowledge of ME/CFS among physicians.[7]
The Vereniging participated in a platform where patient organizations for various disorders aimed to develop a common policy with regard to the development of guidelines and protocols.[8] The first Dutch insurance protocol for CFS, published in 2007[12], was severely criticized by the ME/CVS Vereniging, as was the NICE Guideline for England and Wales[13], alleging that both are misrepresenting the disorder and putting undue emphasis on behavioral therapies.[14][15] The ME/CVS Vereniging participates in the production of a Dutch multidisciplinary guideline for CFS, which is due in 2008/9, a.o. by sharing authorship of chapters on criteria and tests and by providing information on patient experience.[16][17]
The ME/CVS Vereniging is mentioned on most internet pages that deal with ME/CFS and/or patient organizations.[18] It runs the largest ME/CFS patient hyve on the Dutch Hyves.[19]
Finance
Financially, the association depends on membership fees, donations, gifts and project subsidies.[20] The standard contribution per member is 25 Euro annually.
Lees ME
Lees ME is the journal of the ME/CVS Vereniging.[9] New issues appear three times a year. The journal features information, commentaries, interviews, columns, human interest stories, as well as scientific articles, reviews and overviews.
Educational Films
In 2006 the ME/CVS Vereniging asked students from the Hogeschool Rotterdam to make an educational film on ME/CFS. The film features medical expert Dr. Ruud Vermeulen (CVS Research Centrum, Amsterdam) and patients Christine van Reeuwijk and Arno Hogendoorn. On Youtube the film has the highest possible rating. A new group of students made a second film for the ME/CVS Vereniging in 2008. Both films can be found at the association's hyve.
Books by members
- Van Reeuwijk C, "Wie weet morgen. Over leven met een minimum aan energie", Narratio, 2003, ISBN 9052632014
- Schonckert M, "Meer dan moe. Een andere visie op ME/CVS", Houtekiet, 2006, ISBN 9052408718
External links
- ME/CVS Vereniging
- ME/CVS Vereniging on Hyves
- ME/CVS Stichting Nederland (ME/CFS Foundation)
- Stichting Steungroep ME en Arbeidsongeschiktheid (Support Group for ME and Disability)
References: |
|