I’m just coming out of a 4-day M.E. Post Exertional Malaise ‘crash’ and am making the most of my tiny bit of energy this morning to write about my personal observations from the past few weeks of living with M.E./C.F.S. …
Yesterday, Prime Minister Keir Starmer announced that his Government would be ‘scrapping’ NHS England. We have a few opinions on this issue, there is nuance here. Firstly, it goes without saying that job losses are an unwelcome outcome of this …
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 …
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 …
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 …
For a number of years, it has been said amongst the global M.E/C.F.S community that there is an increased risk of suicide amongst our patient population. One research paper responsible for this belief stated; The researchers noted that the overall …
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