Press Releases
Presentation of Declaration to European Commission
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- Category: Press Releases
- Published on Saturday, 30 August 2008 10:07
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MEPs represent regions rather than specific constituencies. The map shows the various regions in the UK. A list of all the MEPs for each region has been compiled and can be found below in alphabetical area by region. You can write to ALL the MEPs listed in your area as that is the only way we can be assured that they will all be aware of fibromyalgia.
You can download a standard letter from here. It will be more successful if you personalise this standard letter when you send it to your MEP's as they are more likely to act.
Full details can be found at http://www.europarl.org.uk/uk_meps/MembersMain.htm
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- National Helpline 0300 999 3333 (10am - 4pm Mon - Fri)
- Benefits Helpline 0300 999 0055 (10am - 12pm Mon, Wed and Fri)
- Complimentary information booklets for doctors and other professionals (fully referenced)
- Books and videos
- Website Contacts with legal specialists
- Conferences
- Local support group and helpline contacts
If your Health Care Professional needs some education in fibromyalgia you can request that an FMA UK Health Professionals Pack is sent out to them. All we need is the name of the Health CareProfessional and the address of their practice. We will then send a pack to their surgery addressed from us to them.
You can request a medical pack using this form.
Trustee meetings are held monthly via Skype and last about 2 hours. There is an annual meeting that coincides with our group leaders’ meeting over a weekend.
You can find a Support Group near you by contacting the Regional Coordinator for your area. If there does not happen to be a support group near you then maybe you can join with some other members and set one up. Support groups provide a social benefit as well as the opportunity to share tips on coping with fibro. They come in all shapes and sizes and we are often told how they have helped people.
