Links to other web Sites

Links to other web sites

Local help/support in Lincs:-

Disability Lincs. - Our office will offer help and information on all matters relating to disability, benefits, and form filling.

Jo Eadie - "Learn to laugh more"

Lincoln Bowen Clinic - "Gentle effective treatments for rebalancing the body & optimum health"

Lincolnshire Neurological Alliance - Bringing together all neurological support groups in Lincolnshire. Liaising with other neurological support groups throughout the UK. Working together to improve the quality of life of all those living with a neurological condition.

Lincs. CFS/ME Services - The NHS CFS/ME services contact details.

VegEPA for ME scheme - The Scheme’s price reductions and shipping costs remain as low as ever. If you’re new to the Scheme then everything is clearly explained on the website.

Overseas M.E./CFS sites and organisations:-

A.H.M.F. - Alison Hunter Memorial Foundation for research into Myalgic Encephalomyelitis / Chronic Syndrome.

CFIDS - Association of America working to conquer chronic fatigue and immune disfunction syndrome.

FM-CFS CANADA - To help the more than one million Canadians affected by Fibromyalgia and Chronic Fatigue Syndrome by advancing education, research and treatment.

ME/FM Action Network - We are a Canadian, registered, non-profit organization dedicated to advancing the recognition and understanding of Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) and Fibromyalgia Syndrome (FMS) through education, advocacy, support, and research.

ME/CFS Society (SA) - The Management of the Society is consciously aware that groups such as this have a danger of developing a negative, self-pity orientated culture. Our desire is to provide a positive, up-beat Society that encourages people to remain positive and take control of their lives.

Office of Research on Women's Health - The Website of the Trans-NIH Working Group for Research on Chronic Fatigue Syndrome sponsored and maintained by the Office of Research on Women's Health.

The Nightingale Research Foundation - Dedicated to the study and treatment of M.E. / CFS

Support organisations for young people:-

The Young ME Sufferers Trust (Tymes Trust)

Association of Young People with M.E. (Ayme)

Action 4 M.E. Young People's Web Site

Regional/local UK support groups:-

Hull & East Yorkshire ME & CFS Self Help Group

Leeds & District ME Group

ME Derbyshire

Norfolk ME Support

Nottingham MESH Group

Sheffield ME Group

York & District ME Support Group

UK M.E./CFS sites & organisations:-

Action for M.E. - Action for M.E. is the UK's leading charity dedicated to improving the lives of people with M.E. We've been at the forefront of the campaign for more research, better treatments and services since 1987, and we provide information and support to people affected by M.E.

BRAINFOG! - Keeping the lighter side of ME/CFS & life ...well and truly ALIVE!

BRAME - Blue Ribbon for the Awareness of M.E.

CFS Research Foundation - Supporting quality research on CFS/ME, its diagnosis and treatment.

EIR - The Environmental Illness Resource is the only site on the web that brings together information on a group of chronic modern conditions that we are calling 'environmental illnesses'. Elsewhere these illnesses may be referred to as '20th century syndrome', 'universal allergy', 'chronic neuroimmune disorders' or 'functional somatic disorders'.

Foggy Friends - The aim of the site is to provide a fun safe place for people to seek help, support and advice, free from harassment.

Invest in ME - Who we are. We are an independent group campaigning for bio-medical research into Myalgic Encephalomyelitis (M.E.), as defined by WHO-ICD-10-G93.3.
We have links nationwide and also internationally.

ME Research UK - MERGE is the Myalgic Encephalomyelitis Research Group for Education and Support. We are a UK charity with the principal aim of commissioning and funding scientific (biomedical) investigation into the causes, consequences and treatment of myalgic encephalomyelitis, or ME.

ME Research UK - Shopping Mall

Network ME - Network ME is a now firmly established registered charity providing vital services to those suffering from ME/CFS in North London and the surrounding counties.

Parents with M.E. - A community for Mums, Dads, Mums-to-be and Dads-to-be who suffer from ME/CFS.

PRIME - The PRIME Project is a collaboration between patients, carers, researchers and service providers who share a commitment to improving our understanding of ME/CFS.

Sleepydust - Helping you to deal with your PVFS/ME/CFS & FMS as best you can, and to get you on to that road to recovery.

The M.E. Association - The ME Association (The MEA), founded in 1976, fulfils its strategic aims by funding and supporting research and providing information and support, education and training. This service benefits people with ME (myalgic encephalopathy)/CFS (chronic fatigue syndrome) and PVFS (post viral fatigue syndrome), professionals and all others interested in the illness.

The National M.E. Centre - Caring for People with Chronic Fatigue Syndrome

The 25% M.E. Group - The 25% M.E.Group exists to support all who have the severe form of M.E. and those who care for them.

UK Parliament - "The Gibson Inquiry", Group on Scientific Research into
Myalgic Encephalomyelitis (ME)

Wikipedia - Chronic fatigue syndrome (CFS), also known as myalgic encephalomyelitis (ME), post-viral fatigue syndrome (PVFS), and various other names, is a syndrome (or group of syndromes) of unknown and possibly multiple etiologies, affecting the central nervous system (CNS), immune, and many other systems and organs.