Forward-ME Group | Minutes of the meeting held on 10 July 2020
Forward-ME Group | Minutes of the meeting held on 10 July 2020 Read More »
Complete lowdown on almost everything that’s happening in the ME/CFS world right now!
Forward-ME Group | Minutes of the meeting held on 10 July 2020 Read More »
Complete lowdown on almost everything that’s happening in the ME/CFS world right now!
Dr Anthony Fauci from the NIH in America, made an important statement about Post-Covid Syndrome and ME/CFS.
Four physiotherapists who became profoundly disturbed by the way their profession was failing to help people with M.E. get better spoke directly to 59,000 colleagues and allied health professionals in their first-ever podcast this week.
While the majority of people with mild illness recover completely in 14 days, doctors say they’re seeing a small percentage like Montano who remain sick for many weeks, or even months.
14,000 people have signed this petition to the European Parliament demanding ME/CFS research.
Meet four teenagers who want to set the world of ME Awareness ablaze. They tell us why!
Focus on young people at next meeting of Westminster APPG on ME | 10am, 16 June 2020 Read More »
Virtual meeting – please email your own MP and ask that they attend this important meeting
‘COVID-19 Can Last for Several Months’ | long read in The Atlantic | 4 June 2020 Read More »
The disease’s “long-haulers” have endured waves of symptoms, and disbelief from doctors and friends.
Rest, Nutrition and Sleep – should be new norm working with patients with PVFS, physios urged.
Up the Blues! This family came together during lockdown – despite living miles apart.
For people with ME/CFS going back to work. Discusses the Returning to Work Risk Assessments.
Two key figures in worldwide ME advocacy – Brian Vastag and Beth Mazur – review the research.
Hannah Collins – there’s good cheer in that right good cuppa!
Two more fundraising champions who are desperate for the ME Association to survive.
Fundraising: Run a little – make it go a long way for the MEA | 8 April 2020 Read More »
Put your daily exercise allowance to the best use – and a note about the new date for the London Marathon
ME Association weekly update: coronavirus and ME/CFS | 7 April 2020 Read More »
Dr Charles Shepherd provides his weekly update for people with ME/CFS
Our latest ME Essential membership magazine – note about the Order Form Read More »
We can’t post out from our office at present, but our leaflets are available online.
Tartan pride: the Moran family take the Kiltwalk in their stride | 2 June 2019 Read More »
They’ve been raising money since 2006 – to honour Jim’s wife Maureen who’s had ME for 30 years.
Fundraising: Jonathan seeks help as he can’t do it all himself! | 9 February 2019 Read More »
Former police officer Jonathan Davis now asks for your support for The ME Association
The world-leading Centers for Disease Control and Prevention has upped the stakes in the fight to get better care for people with ME/CFS.