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 ...
Tag: ME/CFS
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, ...
Severe ME patient Millie’s family tells the Canary the situation is ‘heartbreaking’
A young woman who lives with severe ME is still being dangerously neglected by an NHS hospital - despite interventions, ...
New ME/CFS and long Covid ‘studies’ show junk science and media churnalism are alive and kicking
Two studies - ME, long Covid ones - have been projected into the spotlight thanks to the corporate media. Both ...
Yet another woman with severe ME has been sectioned and abused by an NHS hospital
A young woman living with severe myalgic encephalomyelitis (ME) is being catastrophically neglected by an NHS hospital. Millie's story in ...
Acu Seeds: the BBC is STILL dismissing people’s complaints – so, here’s what to do next
The BBC has been issuing stock responses to chronically ill people over a now-notorious episode of Dragon's Den that featured ...
How much more must people with severe ME tolerate from the UK’s NHS?
In recent months, multiple cases of people living with severe myalgic encephalomyelitis (ME, also referred to as chronic fatigue syndrome, ...
Acu Seeds has devastated chronically ill people. Ofcom must now hold the BBC to account.
This article was updated at 11:40am on Thursday 25 January to reflect a statement from Ofcom. If you live with ...
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