Research: Low-Dose Naltrexone Ineffective for Fibromyalgia
Research: Low-Dose Naltrexone Ineffective for Fibromyalgia Read More »
Low dose naltrexone proves disappointing for fibromyalgia patients in recent trial.
Research: Low-Dose Naltrexone Ineffective for Fibromyalgia Read More »
Low dose naltrexone proves disappointing for fibromyalgia patients in recent trial.
ME/CFS and Long Covid Research: 21 – 27 November 2023 Read More »
The weekly research round-up includes recent publications about ME/CFS and Long Covid.
Many people with Long Covid exhibit an array of symptoms known as autonomic dysfunction (dysautonomia) and include fatigue, post exertional malaise (PEM),
orthostatic intolerance (including postural orthostatic tachycardia
syndrome [POTS]), palpitations, dizziness, exercise intolerance, pain,
brain fog, gastrointestinal symptoms, and temperature dysregulation.
The ME Association Postural Orthostatic Tachycardia Syndrome Survey Results Read More »
The ME Association shares results from October’s Postural Orthostatic Tachycardia Syndrome (PoTS) survey.
BBC News: ‘Long Covid triggered our MCAS, but doctors didn’t believe us’. Read More »
“A growing number of people have secondary illnesses thought to be triggered by Long Covid – including an immune disorder called MCAS…”
ME/CFS and Long Covid Research: 16 – 20 November 2023 Read More »
The weekly research round-up includes recent publications about ME/CFS and Long Covid.
The Big Give Christmas Challenge: Matched Funding Starts on Tuesday! Read More »
Help us to improve health and social care for everyone!
Dr Charles Shepherd responds to MP Jim Shannon about the similarities and overlap of ME/CFS and Long Covid
Living with M.E. A Photographic Study by Jeremy Jeffs Read More »
Photographer Jeremy Jeffs is looking for more people to take part in a project that aims to give identity and visibility to people who are living with M.E.
ME/CFS and Long Covid Research: 06 – 15 November 2023 Read More »
The weekly research round-up includes recent publications about ME/CFS and Long Covid.
Raman research set to continue thanks to Ramsay Research funding from the ME Association Read More »
The ME Association (MEA) is pleased to announce that the
TIME Magazine: A new radical approach needed for Long COVID research Read More »
With no treatment or cure in sight for Long Covid patients, who is really to blame for 3 years of disappointing clinical research results?
Rapamycin Pilot Treatment Trial for ME/CFS Read More »
Rapamycin therapy inhibits mTOR and reduces autophagy disruption. We believe
ME/CFS and Long Covid Research: 31 October – 6 November 2023 Read More »
The weekly research round-up includes recent publications about ME/CFS and Long Covid.
The DHSC have published an update on the Interim Delivery Plan now consultations are closed and they are considering all responses received.
Following our complaint about some offensive wording in a job
New Booklet now available: Ten Key Aspects of Management Read More »
Dr Charles Shepherd, Trustee and Honorary Medical Adviser to The
ME/CFS and Long Covid Research: 24 – 30 October 2023 Read More »
The weekly research round-up includes recent publications about ME/CFS and Long Covid.
Embracing disability and neurodiversity in the workplace Read More »
Claire Munn MSc MCIEEM Extracts The unknown is understandably often
Invite your MP to the next All-Party Parliamentary Group meeting on M.E. Read More »
People are being asked to invite their local MP to the next APPG meeting in November.