In an increasingly complex world, educating professionals with a duty of care—such as those in healthcare, education, and employment—has never been more critical. These individuals are on the front lines, responsible for the wellbeing of others, and their actions can …
Clarifying Long COVID Subsets: The Importance of Differentiation in Media Coverage of the REGAIN Study As the scientific community delves deeper into understanding Long COVID, it becomes increasingly crucial for the media to accurately differentiate between its subsets. In light …
Dear Members of the Public and Medical Professionals, As we reflect on the recent episode of Dragon’s Den, and subsequent backlash, that shed light on Myalgic Encephalomyelitis, also sometimes called Chronic Fatigue Syndrome (M.E./C.F.S), it’s crucial to recognize the pressing …
We know that Governments simply go from election promise to election promise, whatever works on the doorstep seem to become priorities and manifesto pledges. Long term planning doesn’t seem to be a skill politicians have. The issue of palliative-style care …
There may not be any effective treatments or cures for Myalgic Encephalomyelitis also sometimes known as Chronic Fatigue Syndrome (M.E/C.F.S.), but people living with M.E/C.F.S find themselves on hospital estates for a variety of reasons including appointments for tests for …
COMMENT The Myalgic Encephalomyelitis / Chronic Fatigue Syndrome community already stands at an estimated 1.25 million people in the UK. The majority of whom developed M.E/C.F.S as a direct result of catching COVID19. How much more will our patient numbers …
This blog is being written in response to Emily Maitlis’ lecture at the James MacTaggart Memorial Lecture of 24th August 2022, her lecture resonated with us and the issues she raised, in relation to journalism and politics, reminded us of …
#MindsetReboot Campaign Exercise is a good thing……Right? Most people need more physical activity……Agreed “There is no situation, there is no age, and no condition where exercise is not a good thing” This was stated by Sir Chris Whitty, Chief Medical …
Our vision is to improve the quality of life of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome patients. How do we do this? The experience of having the disease is bad enough but patients also have to deal with poor ‘treatment’ and support …
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