Participation request! Please help the Norwegian ME Association (Norges Myalgisk Encefalopati Forening) gather crucial information about ME/CFS by filling out their survey:
The Norwegian ME Association has developed this excellent survey to fill knowledge gaps about the course of illness with ME/CFS. This effort will help inform policy decisions and the health and social care provided.
M.E. charity statement on the Covid vaccine We are receiving a very high number of enquiries from people…
That this House marks the retirement of the Countess of Mar as the Founding Chair of Forward-ME; congratulates…
We are very disappointed to hear of the ‘pause’ in publication of the NICE ME/CFS Guideline, already delayed…
Useful medical information when treating COVID-19 in patients with underlyingmyalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and severe fibromyalgia (FM)…
The 25% ME Group is campaigning for better care to prevent malnutrition in people with severe ME. The…
The ME Association is pleased to announce the establishment of the Howes Goudsmit Prize for Severe ME research….