Myalgic Encephalomyelitis - ME - Chronic Fatigue Syndrome - CFS - Post-Viral Fatigue Syndrome - PVFS - Chronic Fatigue Immune Dysfunction Syndrome - CFIDS ? No matter which name or abbreviation you use, the illness affects people of different ages, backgrounds, race, and most other characteristics you may choose to consider.

The illness often follows a period of viral infection, but some sufferers experience a gradual decline into the illness.

Many sufferers experience all or at least some of the following symptoms to differing levels of severity:

- blurred vision
- decreased concentration levels
- disturbed sleep patterns
- incapacitating pain
- increased sensitivity to light, smell, sound and touch
- decline in clarity and coherence of speech
- memory impairment
- muscle weakness and spasms
- painful joints & muscles
- severe fatigue
- stomach and digestive problems

For the lucky few the illness has limited effect, but others experience major disruption to their lifestyle and may become house or bed-bound and totally reliant on their carers for months or years.

Some sufferers make a slow recovery to near optimum health, others make a partial recovery and may suffer relapses, others remain seriously affected by the chronic illness for many years.

Is there a cure? Unfortunately not yet! You will doubtless read of people who have recovered from the illness by following a particular therapy or regime, either mainstream or alternative, but as at April 2006 there is no treatment which is guaranteed to cure the illness. The good news is that researchers are making progress, and many sufferers and their carers cannot wait for the day when 'cure' becomes a reality.

Welcome SMEG members

So how does this website aim to help you?

We aim to:

- Encourage you to increase your personal knowledge and understanding of ME, CFS, CFIDS by visiting the websites of various organisations throughout the UK and other countries.
- Keep you in touch with the latest ME - CFS - CFIDS news by visiting our weblog.
- Give you the opportunity to discuss your views about ME - CFS - CFIDS with others by visiting our forums.

If you wish to visit the main content areas of our site, please click either here or the button below - Thanks

Continue to the main content area


The administrators of the 'Living With ME' website, volunteers and employees do not advocate the use of any particular type of medication, treatment or healthcare.
YOU should ALWAYS seek advice from a DOCTOR / GP / CONSULTANT before undertaking any treatment.
 
. . . . . . . . . . . .