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…
On Friday 15 March campaigners from Not Recovered UK – who all either live with long Covid, myalgic encephalomyelitis (ME, sometimes known as chronic fatigue syndrome, CFS), or are impacted…
In recent months, multiple cases of people living with severe myalgic encephalomyelitis (ME, also referred to as chronic fatigue syndrome, CFS) being neglected and mistreated by the UK’s NHS have…