The Sussex ME Society who support those in the county affected by ME has welcomed a recently published guideline for medical professionals that are caring for those most severely affected by the disabling illness.
The Sussex ME Society who support those in the county affected by ME has welcomed a recently published guideline for medical professionals that are caring for those most severely affected by the disabling illness.
The Sussex ME Society who care for those affected by ME or Chronic fatigue syndrome are holding a conference focusing on the treatment of the illness and current research at the Brighthelm Centre on October 6.
The charity that cares for those in the region affected by Myalgic Encephalopathy (ME) or Chronic Fatigue Syndrome (CFS) has a new website designed to cover the latest local and national news and developments in an easily understood format.
Myalgic encephalopathy (ME) or Chronic fatigue syndrome (CFS) affects around 6,000 people across Sussex many of whom are housebound and in need of care. During the October UK CFS/ME Research Collaborative conference in Newcastle, neurologist Dr Mark Edwards announced that a team of scientists wants to test a new theory for how functional symptoms can arise from the brain.
The Sussex charity that works for the 6,000 people affected by Myalgic Encephalopathy(ME) or Chronic Fatigue Syndrome(CFS) across the county has welcomed important new research into the illness. A study by scientists at Stanford University School of Medicine has discovered differences in the brains of healthy people and people with ME.
