All Party Parliamentary Group on Myalgic Encephalomyelitis
All Party Parliamentary Group on Myalgic Encephalomyelitis Read More »
The All-Party Parliamentary Group (APPG) on Myalgic Encephalomyelitis (ME) (APPG […]
All Party Parliamentary Group on Myalgic Encephalomyelitis Read More »
The All-Party Parliamentary Group (APPG) on Myalgic Encephalomyelitis (ME) (APPG […]
Differential diagnosis of ME/CFS: Prolactinoma Read More »
A new paper, titled “The Dutch Prolactinoma Cohort Studies: Cross-sectional
Tessa Munt MP writes to new Minister for Health Innovation about ME/CFS Read More »
Tessa Munt ©House of Commons/Roger Harris, cropped and shared under
Update: UK ME/CFS Biobank Steering Group: June Meeting Read More »
The ME Association (MEA) has supported the operational costs of the
Research update: Can we reach consensus on ME/CFS research criteria? Read More »
We are 11 months into a research project led by
Treatment: Clinical trials into the use of LDN in ME/CFS, Long Covid and Fibromyalgia Read More »
On the 12th of August, Pain Management Nursing published an
Timms Review Workshops: Disabled People Invited to Help Shape Future PIP Recommendations Read More »
The UK Government’s Timms Review of Personal Independence Payment (PIP) has opened
Forward ME chair shares a message on Severe ME Day Read More »
Severe ME Day (08.08.26) For most people, it is a
Rebecca’s story: speaking out to advocate for greater awareness during Severe ME Week Read More »
“The reality is that there is currently no clear treatment
Hailee’s story: lived experience with severe ME Read More »
“Hope is what keeps me going. It is what helps
WAMES met with Health Minister to discuss ME and Long Covid services in Wales Read More »
Photo of Mabon ap Gwynfor Image cropped (original image here),
Help Shape the Future of NHS Care: HERITAGE is Now Recruiting! Read More »
What is the HERITAGE study? The HERITAGE study aims to address an
Naomi’s story: lived experience of Severe ME Read More »
“I want to share my lived experience of severe ME as I
Forward ME Briefing Paper on Clinical assessment of people with very severe ME/CFS Read More »
Dr Charles Shepherd, MEA Hon. Medical Adviser, has written a
Nature has published a research study entitled The genetic architecture
NHS England’s ME/CFS e-Learning Modules FOI Results reveal lack of uptake Read More »
In January 2026, and repeated in June, @Lucibee, an advocate for people with ME/CFS submitted
ME/CFS Service Closures Without Consultation: What You Need to Know Read More »
Across the UK, there are growing reports of ME/CFS specialist
DHSC Delivery Plan on ME/CFS – One year on Read More »
The Department of Health and Social Care (DHSC) Delivery Plan
Today (23rd July), the iPaper published an article entitled ’75
Image Credit: Yvette Cooper © House of Commons/Roger Harris, cropped