The Sussex ME/CFS Society is the registered charity that informs, supports, and represents many of those suffering from the illness.
The Sussex ME/CFS Society is the registered charity that informs, supports, and represents many of those suffering from the illness.
The Sussex ME Society welcomes a research publication that identifies specific brain abnormalities found in the illness.
Sussex ME Society prepare to host conference on Myalgic Encephalopathy (ME) or Chronic Fatigue Syndrome (CFS) for patients and medical professionals at the Brighthelm Centre in Brighton 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.
