219K views · 1K reactions | This 21-year-old woman died after suffering with ME for six years. Her family were told by medics that the condition didn't exist - they hope Merryn's story can inspire a change in treatment. MErryn’s Legacy | ME Association | Channel 5 News | Facebook

At the ME Association, we believe that research holds the key to transforming the lives of people with ME/CFS and Long Covid. Since establishing the Ramsay Research Fund in 1989/1990, we've been committed to funding high quality biomedical research into ME/CFS. So far, we’ve invested £2.6 million into research — with another £2 million planned over the next three years. None of this would be possible without your continued support. Thank you for helping us make a difference! Find out more: https

Tomas et al. (2019) Assessing cellular energy dysfunction in ME/CFS using a commercially available laboratory test. Biomarker research is important because biomarkers—measurable biological indicators of disease—may help diagnose ME/CFS. This is one of several studies that needs replication before any firm conclusions can be made as to its accuracy and to ensure it is specific to ME/CFS. Read more about the study, funded by the ME Association's Ramsay Research Fund, here: https://www.nature.com/a

4.5K views · 74 reactions | This month, the ME Association announced...