Our Core Beliefs

ME, (also sometimes known as CFS and PVFS), is a physical, relapsing illness with scientifically demonstrated disturbances of the neurological, endocrine, vascular and immune systems. It is characterised by physical and mental exhaustion following activity. Activity can also lead to the onset or worsening of other symptoms.

The cause of the illness is not yet known but its onset is often associated with viral infection. No cure or universally effective treatment has yet been found. It is possible for people with ME to improve or recover through the body's own ability to heal itself.

Of those who recover, some experience relapses. It is not known whether this may be a life long possibility. Of those who remain ill most are unable to work to full capacity. Some gradually return to a limited form of work but for many recovery is restricted and independent living is their main goal. 25% are severely affected and largely housebound or bedbound.

The aims of Network MEsh West London are to:
 Increase public awareness of ME as described above.
 Press for biomedical research to find the cause or causes of ME and to find diagnostic biomarkers, effective treatments and a cure for the illness.
 Help members obtain appropriate services, including medical care, welfare benefits, social services and education; particularly recognising the need for home based services for the severely affected.

ME is recognised as a neurological illness by the World Health Organisation (ICD-10. G.93.3) and as a serious chronic condition by the Chief Medical Officer of England.