September 15, 2009

Carmarthenshire ME Group

Contact: John James.
Telephone: 01267 233793 (afternoons only, please.)
Meetings are usually held every other month month at Coleshill Social Centre, Coleshill Terrace, Llanelli SA15 3BT at 2pm. Ring to confirm dates.

FibroSupport – Wales

Facebook: FibroSupport-Wales
Twitter: @FSWales

FibroSupport-Wales is a group where people with Fibromyalgia can come and feel listened to and no longer feel alone. It provides a safe non-judgemental environment both online and at our meetings.
We also give advice, support, signposting as well as meet ups, social events, peer support and so much more. We have a strong online group with over 1600 members at present who contribute massively to each other whilst maintaining our values.

Llandrindod Wells FM/ME/CFS Support Group

Contact: Kat Palmer
Telephone: 07845152519
Facebook: Llandrindod Wells, Builth and surrounding ME & Fibro Support Group

We hold a free meeting each week at Ashfield Community Enterprise, Howey, LD1 5PN. On Mondays from 11.30am – 1.00pm staring 6th January and then every other week. And, on Tuesdays from 6.30pm – 8.00pm starting 14th January and then every other week.

ME Support in Glamorgan (MESiG)

Contact: Miriam Wood (MESiG Political Liaison)

A charity supporting those with ME/CFS, Fibromyalgia and Lyme Disease. We have been established since 1988, revived and renamed in 2004 / 2005 by a small group of volunteers with personal experience of M.E or Fibromyalgia and Lyme Disease, who wanted to see change.
Whether you suffer from the debilitating effects of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome, (more commonly referred to as ME/CFS), Fibromyalgia or Lyme Disease or are supporting a family member or friend we hope you will find us informative and friendly.
We also welcome all in the medical field, social services, benefit agencies and support agencies as our aim is to raise awareness and services for people with these conditions. MESiG covers all ‘CF’ postcodes and further afield.
The group meets once a month on first Monday at 2pm in Bethel Church Hall, Llangranog Rd, Llanishen, Cardiff, CF14 5BJ.

Milford Haven FM/ME/CFS Support and Carers Group

Contact: Chair: Gary Yates or Secretary: Carol Yates.
Telephone: 0844 887 2385 or Mobile: 07867 482 929.
Facebook: FM/ME/CFS Support & Carers Group West Wales

The group is open to all ages. Meetings are held on the first Tuesday of every month 10.00am-1.00pm at Milford Haven Christian Fellowship, Marine House Nantucket Avenue, Milford Haven Pembrokeshire SA73 2BE.

Montgomeryshire ME/CFS and FM Group

Contact: Mike or Karen.
Telephone: 0796 966 5419 (between 2.00pm and 4.00pm only please.)
Email: for more information and date of the next meeting.

North Wales CFS/ME Community

Facebook: North Wales CFS/ME Community
Facebook Group: A community and information group individuals and friends impacted by Chronic Fatigue Syndrome (CFS) / Myalgic Encephalomyelitis (M.E.). A place for sharing information, discussion and correspondence.

Pembrokeshire – CWTCH

Contact: Beth Job: Mobile: 07974 543 874
Contact: Mia Harries: Mobile: 07530 870 024

‘CWTCH' stands for Care and Well-being Through Chronic Health. The group is open to adults aged between 18 and 45. The group meets on the first Friday in every month (except during school holidays) at Cashfields Community Centre, The Patch, Haverfordwest SA61 1HQ, 10am-11.30am. Admission is free.

Welsh Association of ME and CFS Support (WAMES)

Contact: Jan Russell.
Telephone: 01970 636515
Helpline: 029 2051 5061

We are a campaigning organisation, seeking to influence the development of health, social care and education policy in Wales in the interests of all people with ME & CFS and their carers. We also campaign outside Wales on issues directly affecting Welsh residents.

West Wales ME and FM Group

Contact: Tina Norman (Host)
Telephone: 01437 454 359

The group meets on the last Monday in each month at 65 Tudor Gardens, Merlins Bridge, Haverfordwest, 11.00am – 1.00pm. Before travelling, please check on the day that all's well.

The ME Association

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