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Presentation of Declaration to European Commission
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- Published on Saturday, 30 August 2008 10:07
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Written declaration on fibromyalgia presented by the European Network of Fibromyalgia Associations (ENFA)
The European Parliament,
– having regard to Rule 116 of its Rules of Procedure,
- whereas nearly 14 million persons in the EU and 1 to 3 % of the general population worldwide suffer from fibromyalgia, a debilitating condition resulting in chronic widespread pain,
- whereas WHO has recognised fibromyalgia as a disease since 1996, but it is still not coded in the official index of conditions in the EU, which excludes patients from formal diagnosis,
- whereas patients with fibromyalgia make more GP visits, have more specialist referrals, are issued more sick notes and receive more in-patient services, thus generate a considerable economic burden for Europe,
- whereas people with fibromyalgia struggle to lead full and independent lives, unless they have access to appropriate treatment and support.
- Calls on the Commission and the Council to:
- Develop a Community strategy on fibromyalgia in order to recognize this condition as a disease;
- Help raising awareness of the condition and facilitate access to information for health professionals and patients, by supporting European and National Awareness campaigns;
- Encourage Member States to improve access to diagnosis and treatment;
- Facilitate research on fibromyalgia through the work programmes of the EU 7thFramework Programme for Research and future research programmes;
- Facilitate the development of programs for collecting data on fibromyalgia.
- Instructs its President to forward this declaration, together with the names of the signatories, to the Council, the Commission and the parliaments of the Member States.