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The woman being denied the NHS care she needs to treat her ME
This is the inpatient experience of a patient with very severe ME, whose father Michael Gordon gave an…
Open letter from Parents and Carers
An open response from parents and carers of people with Severe Myalgic Encephalomyelitis to ‘Management of Nutritional Failure…
Charities request for the removal oF harmful treatments
As charities supporting people with M.E. we have been actively campaigning for NICE to remove the recommendation of…
Call for people to take part in a ME research study
The ME Association is funding a study led by Prof Sarah Tyson of University of Manchester (who also…
The Power of Listening
Introduction As a doctor, and perhaps especially as a junior doctor, there will no doubt be occasions when…
Key genetic differences found in people with chronic fatigue syndrome.
Abstract Myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) is a common, poorly understood disease that has no effective…