For South Asian women, it’s not just medical gaslighting that pervades their ME/CFS diagnoses
Shehla Ali from About M.E. looks at the racism and discrimination that pervades healthcare for South Asian women living with ...
Tag: ME/CFS
A decade of advocacy fighting for ME/CFS has left me angry and frustrated
As part of the Canary and the Chronic Collaboration's Amplify training programme, founder of ME Foggy Dog and Stripy Lightbulb ...
It’s 2024, and yet there’s still no general election for ‘ME’
It doesn't really matter who gets elected during this years general election for the 1.9 million people living with long ...
A council is promoting a junk science exercise programme for long Covid patients
A council in Northamptonshire has launched a recovery scheme for people living with long Covid. However, the 12-week long Covid ...
Quack science the ‘Lightning Process’ strikes the chronic illness community again – this time, long Covid
The BBC has exposed how an insidious group of predatory charlatans have been gaslighting long Covid patients. It revolves around ...
A groundbreaking community-led conference is set to shake up the scene for people with long Covid and ME/CFS
A groundbreaking international and community-driven long Covid and myalgic encephalomyelitis (ME/CFS) conference - 'Unite To Fight' - is about to ...
Australia’s state and services are trapping a woman living with severe ME/CFS in domestic abuse
A woman living with severe myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) in Australia is desperately appealing for help to leave an ...
Biomedical research funding into ME/CFS abysmal, so a campaign is calling on YOU to take action
A new campaign seeks to shake up the dire state of funding for biomedical research into myalgic encephalomyelitis (ME). In ...
The two leading UK ME/CFS charities are linked to an organisation fomenting the psychologisation of the illness
Two of the biggest myalgic encephalomyelitis (ME) charities in the UK may be a little too cosy with a controversial ...
The family of ANOTHER young woman with very severe ME are scared their daughter is going to DIE in an NHS hospital
After public outcry and media coverage around a campaign called #BringMillieHome, it has come to light another young woman - ...
An ME inquiry? Not likely when a pillar of the psychologising establishment has access to the halls of power
Guardian journalist George Monbiot has been calling out the continued appalling abuse of people living with myalgic encephalomyelitis (ME, also ...
NHS ramps up medical abuse of two people with ME/CFS – as new Europe-wide survey shows it’s systemic
The NHS is continuing to unconscionably abuse two women living with severe Myalgic Encephalomyelitis (ME/CFS) - and putting their lives ...
Forced treatments, sectionings, deaths, assisted suicides: the reality of ME/CFS in the UK in just THREE MONTHS of 2024
The NHS killed Sophia Mirza on 15 November 2005. Sophia lived with myalgic encephalomyelitis (ME/CFS). In July 2003, psychiatrists got ...
The likes of the BBC, Guardian, and Daily Mail are set to have their own disinformation used against them
A campaign group will be targeting UK media outlets during global ME Awareness Day - calling out what it calls ...
Trivialising long Covid? Scientists and media covering ME/CFS in Australia wrote the playbook
A group of Australian scientists recently gas-lit an entire global community of more than 65 million sick people. Specifically, on ...
‘LONG COVID DOESN’T EXIST’ scream the corporate media. Well, #LongCovidAwarenessDay proved them wrong.
Friday 15 March was global Long Covid Awareness Day. In London, a campaign group brought together other activists, patients, and ...
On Long Covid Awareness Day patients will be taking over Westminster to make noise & raise awareness
On Friday 15 March campaigners from Not Recovered UK - who all either live with long Covid, myalgic encephalomyelitis (ME, ...
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