We are delighted to announce that we have grown our social media and online presence to include Instagram. Social media plays a big part of our modern digital age and we recognise that for many with M.E/CFS, this valuable tool...
Read moreThe ME Association has released its 10th edition of the Purple Book, a must have guide for anyone who has been affected by, or has an interest in M.E/CFS. This 147 page book has undergone a 6000 word revision with...
Read moreMyalgic encephalomyelitis/chronic fatigue syndrome does not currently have a diagnostic test. But this may soon change, as researchers have developed a test that can predict it with an unprecedented level of accuracy. Currently, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is estimated Read more…
A gut reaction is the problem in ME/CFS – that’s the main idea being pursued by Dr Ian W. Lipkin of the Center for Infection and Immunity at Columbia University. He believes that the body’s response to changes in the Read more…
Forward-ME Group Letter Forward-ME Group Chair, The Countess of Mar, has written on behalf of the members of the Group to the Chief Executive of the Science Media Centre asking for the SMC “to retract and replace your factsheet on Read more…
The ME Association has teamed-up with Gary Burgess to produce a series of podcasts they have called ‘The ME Show’. Gary will be narrating each episode and interviewing invited guests. The podcasts will seek to raise awareness about M.E., provide Read more…
ITV News, 23 April, 2018 Ministers urged to go further in disability benefits reform after major review Frank Field, chairman of the Work and Pensions select committee. MPs and campaigners have urged the Government to go further in reforming benefits Read more…
On Friday 12th of May the Millions Missing campaign will be held in Birmingham. Last year’s event was a great success with the many pairs of shoes laid out on the path capturing the attention of passers by. This year Read more…