If you require resources or an enquiry pack please use the Resource Request form here. To have a medical pack sent to your GP use this form.
Requests for support groups or contacts must include a post code. A landline would also be helpful in case we cannot contact you by email. Please check groups below to ensure your enquiry is going to the correct area!
If someone does not get back to you after a week, please contact the office.
Regional Coordinators
Our Regional Coordinators below can put you in touch with a group nearest to you. Please fill out the form after selecting the RC for your area and someone will get back to you as soon as they can. If looking for your nearest support group please include your post code. Please remember that they are volunteers with fibromyalgia and may take a few days to get back to you. If someone does not get back to you after a week, please contact the office.
These contacts are for people to find their local support groups and are not to be used for commercial purposes. Messages about products received through these contacts will be ignored. If you would like your product considered please contact head office.
Highlights
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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.
