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.
The ME Association Big Give Christmas Challenge starts today! Read More »
We hope to raise £25,000 during this matched-funding period (to reach a total of £50,000).
The Times: ‘Hospitals have no services for most severe ME cases, coroner told’ Read More »
Maeve Boothby-O’Neill, the daughter of the Times journalist Sean O’Neill, died 2 years ago after becoming bedbound.
ME Association Research Review: Mortality in ME/CFS Read More »
Malnutrition is the most serious life-threatening complication in those with ME/CFS, especially in very severe cases.
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.
The ME Association writes to the CEO of Cheshire and
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
Research: Long Covid treatment trial: Donepezil hydrochloride Read More »
The effect of donepezil hydrochloride on post-COVID memory impairment: A
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.
The Advertising Standards Agency (ASA) challenged whether the claims that
There are new scientific insights into long Covid – but
