Building an NHS that’s there for people with Long Covid and ME
Building an NHS that’s there for people with Long Covid and ME Read More »
#ThereForME is a patient- and carer-led campaign calling for an […]
Building an NHS that’s there for people with Long Covid and ME Read More »
#ThereForME is a patient- and carer-led campaign calling for an […]
We hope the protocol when implemented will bring relief to the hundreds of thousands of people who suffer from these very debilitating symptoms
America: What’s Wrong With the National Academies’ Long Covid Definition? Read More »
The specificity is rather poor, which translates into inaccurately diagnosing many who do not have Long Covid.
Carers Week 2024: Putting carers on the map! Read More »
The ME Association has joined other charities to highlight the invaluable contribution that carers make across the UK.
New York Times: New report underscores the seriousness of Long Covid Read More »
An important report from the National Acadamies in America with comparisons to ME/CFS and FM.
A great article from The Guardian with opinion from Dr Binita Kane on ME/CFS and Long Covid.
Carers UK: Open letter from unpaid carers to the future Prime Minister Read More »
The ME Association is an official sponsor of Carers Week
A new support pack for anyone with ME/CFS going to hospital Read More »
The pack aims to address the many issues facing people with ME/CFS when they attend hospital.
Endorsed by UK CRC, DHSC, UKRI MRC, NIHR, and CSO in Scotland.
Editorial: Medical students highlight importance of ME/CFS medical education Read More »
Medical students at Scottish medical schools were invited to take part in an essay competition on ME/CFS.
NHS England Launches New E-learning Module on ME/CFS! Read More »
The new e-learning module was launched at the BACME conference…
The ME Association: ME/CFS and Long Covid at the Disability employment inquiry Read More »
The committee was focused on ‘barriers to work’ which is not an easy subject to talk about…
Parents of children with Long Covid accused of making it up Read More »
“There is a cultural problem that is ingrained within medicine to not believe patients if we can’t explain their symptoms…”
ME Association Statement: Improving healthcare for people with ME/CFS and Long Covid Read More »
The ME Association is committed to working with the NHS and social care providers to improve healthcare for people with ME/CFS and Long Covid.
Research: Sex and disease severity‑based analysis of steroid hormones in ME/CFS Read More »
Study found that levels of steroid hormones in were significantly different in ME/CFS…
How many people have ME/CFS in the UK? Read More »
The honest answer is that we just don’t know how many people have ME/CFS in the UK.
The Times: “People with ME have been ignored for far too long” Read More »
“This Sunday, World ME Day, is an opportunity to refocus minds on how much more needs to be done.”
“We urgently need to come up with answers to help those struggling with Long Covid feel whole again.”
Research: Working together to find answers to ME/CFS! Read More »
There are 4 workshops taking place this summer for researchers, clinicians and people with ME/CFS.
Parliamentary question: Hospital compliance with NICE Guideline on ME/CFS Read More »
Baroness Scott tabled a question about hospital compliance with the NICE Guideline on ME/CFS.