The ME Association End of Week Research Round-up | 17 January 2020
The ME Association End of Week Research Round-up | 17 January 2020 Read More »
This is a new feature that we will be doing at the end of every week as a result of your feedback.
The ME Association End of Week Research Round-up | 17 January 2020 Read More »
This is a new feature that we will be doing at the end of every week as a result of your feedback.
Kate Stanforth’s childhood dream of becoming a professional dancer was crushed due to a chronic condition.
“My life has completely changed. I try to explain how it feels, it’s like a past life really.”
Conor Hope has been bedbound for the past 18 months with ME/CFS and is desperate for specialist support from the NHS.
America: Patients push limits for clues to ME/CFS | 09 January 2019 Read More »
Doctors at the NIH are using volunteers for a unique study that pushes their limits in search of what’s stealing all their energy.
ME Association December Summary of ME/CFS Published Research | 08 January 2020 Read More »
We’ve updated the free Research Index and feature 18 research studies from December 2019.
In this month’s survey we are hoping you will support the proposed major study on genetics.
Results suggest that glycolysis, a less efficient method of energy production, may be disrupted in ME/CFS.
ME Association November Summary of ME/CFS Published Research | 10 December 2019 Read More »
We’ve updated the free Research Index and feature 17 research studies from November 2019.
MEA Summary Review: Low Dose Naltrexone (LDN) in ME/CFS | 02 December 2019 Read More »
We have updated this research review to include a new study from Finland.
“Get Well Soon” – Guest Blog by Louise Shepherd | 22 November 2019 Read More »
Such small but powerful words – for right and wrong reasons… When there’s no chance of becoming 100% better, hearing or reading them can really drag you down to the dark places of your mind.
The MRC will host a workshop to help the CMRC with its major bioresource proposal involving 20,000 samples and data from people with M.E.
ME Association October Summary of ME/CFS Published Research | 06 November 2019 Read More »
We’ve updated the free central Research Index and feature 16 research studies from October 2019.
We Respond to NICE ‘Suspected Neurological Disorders’ Quality Standard | 25 October 2019 Read More »
Ewan Dale explains how the MEA has responded to this latest consultation from NICE and we review the controversial clinical guideline.
We’re at the Royal College of GPs conference in Liverpool! | 24 October 2019 Read More »
The RCGP conference is underway and we’re there with Forward ME. Medical student Emilia Allwright has presented her research based on your responses to a recent survey.
“The ME Association is delighted to announce that our Ramsay Research Fund has been able to make three major research grants totalling nearly £200,000.”
MEA Summary Review: Differentiating Medical Uncertainty | 21 October 2019 Read More »
We take a closer look at recent research from America that highlights concerns over inappropriate and harmful labelling and advocates for medicine to adopt a more patient-centred approach to care.
Following a SMC briefing, many news-media outlets report on the claim that chronic lyme disease is likely to be CFS.
ME Association September Summary of ME/CFS Published Research | 05 October 2019 Read More »
We’ve updated the central Research Index and feature 12 ME/CFS research studies from September 2019.
Pippa explains what this national campaign has meant to her and we update on a recent meeting with Sport England.