The International ME/CFS Family Impact Study
The International ME/CFS Family Impact Study Read More »
Dr Muirhead and Cardiff University need to hear your experiences of how ME/CFS affects the Quality of Life of patients, carers, and family members.
Quality of Life
New Leaflet: Pensions – obtaining an ill-health pension, prognosis & permanency in ME/CFS
We have published a new leaflet to help people who want to claim early retirement on the grounds of ill-health because of ME/CFS.
New! ME/CFS Family Impact Survey by Dr Nina Muirhead & Cardiff University
New! ME/CFS Family Impact Survey by Dr Nina Muirhead & Cardiff University Read More »
Please complete this quick survey to help improve international understanding of how ME/CFS impacts patients and family members.
New MEA Leaflets: Prognosis & Quality of Life, Disability Classification & Illness Severity
The new leaflets explain what might be expected from a diagnosis of ME/CFS and how the illness is classed as a disability by the UK Government.
The ME Association Research Round-up
The ME Association Research Round-up Read More »
This week we feature a new study that examines acute Epstein Barr as a trigger and another that reports on use of IV Saline as a potential treatment.
The ME Association End of Week Research Round-up
The ME Association End of Week Research Round-up Read More »
We highlight 3 studies from last week’s 6 ME/CFS research publications.
Severe ME Week: How might healthcare be improved?
Severe ME Week: How might healthcare be improved? Read More »
In this introduction you will find a discussion about the need for suitable healthcare. Also background about severe and very severe M.E. and the support that is available.