research featured in a campaign to shake it up
A new campaign seeks to shake up the dire state of funding for biomedical research into myalgic encephalomyelitis (ME). In time for ME Awareness Day on 12 May, a volunteer…
A new campaign seeks to shake up the dire state of funding for biomedical research into myalgic encephalomyelitis (ME). In time for ME Awareness Day on 12 May, a volunteer…
Two of the biggest myalgic encephalomyelitis (ME) charities in the UK may be a little too cosy with a controversial organisation pulling the strings behind the clinical care for patients…
After public outcry and media coverage around a campaign called #BringMillieHome, it has come to light another young woman living – Carla – with ‘severe ME’ (myalgic encephalomyelitis, ME, also…
Guardian journalist George Monbiot has been calling out the continued appalling abuse of people living with myalgic encephalomyelitis (ME, also known as ME/CFS). However, there’s one prominent, powerful psychiatrist standing…
The NHS is continuing to unconscionably abuse two women living with severe Myalgic Encephalomyelitis (ME/CFS) – and putting their lives at risk. As it metes out this horrendous crusade of…
The NHS killed Sophia Mirza on 15 November 2005. Sophia lived with myalgic encephalomyelitis (ME/CFS). In July 2003, psychiatrists got cops to smash the door into Sophia’s home down and…
A campaign group will be targeting UK media outlets during global ME Awareness Day – calling out what it calls the corporate media’s systemic “mis-and-disinformation” relating to this chronic illness.…