‘Chronically Ill – Chronically Ignored’: a new documentary on ME/CFS
One of the “biggest medical scandals of the 21st century” is about to be blown wide open to a new ...
Tag: ME/CFS
Psychiatrists in Denmark STILL plan to forcibly detain a severe ME/CFS patient
Psychiatrists in Denmark are still threatening to forcibly detain a severe myalgic encephalomyelitis (ME/CFS) patient in a psychiatric hospital. They ...
Yet another severe ME/CFS patient is being threatened with detention in a psychiatric ward
It’s 2025, but the abuse of people living myalgic encephalomyelitis (ME/CFS) continues unabated. Already, less than a month into the ...
Does new ME/CFS research finally prove that long Covid is the same thing?
A research paper into myalgic encephalomyelitis (ME/CFS) has claimed that the majority of long Covid patients live with it - ...
A woman from Canada with severe ME has been approved for MAiD – but she wants to live
After decades battling severe ME/CFS and systemic lack of support, Marcia Doherty - known online as "Madeline" - is going ...
The government’s response to Maeve’s inquest report is dire for severe ME patients
Health minister Andrew Gwynne has shown how little the new Labour Party government will actually do to fix the abysmal ...
A severe ME/CFS patient in Pakistan is urgently fundraising for crucial surgery
In Pakistan, severely chronically ill disability advocate and survivor of domestic violence Nevra Liz Ahmed urgently needs surgery for a ...
DWP strips severely chronically ill mother and disabled son of £8k a year in Universal Credit migration
The Department for Work and Pensions (DWP) Universal Credit mandatory managed migration has stripped a severely chronically ill and largely ...
A hospital in New Zealand discharged a young severe ME/CFS patient to a care home for pensioners
A hospital in New Zealand discharged a 34-year-old severe myalgic encephalomyelitis (ME/CFS) patient to a care home for pensioners. There, ...
A young woman with severe ME/CFS in Pakistan needs an in-person advocate – can you help?
A young woman, Nevra, who lives with severe myalgic encephalomyelitis (ME/CFS) is issuing an urgent call out for an in-person ...
Very severe ME/CFS patient LOSES appeal over sectioning, family says staff now ‘abusing’ her
Carla, a very severe myalgic encephalomyelitis (ME/CFS) patient has lost her appeal against West Middlesex hospital. Doctors sectioned Carla Naoum ...
The NHS public consultation is NOT accessible for chronically ill people. So, the Canary has stepped in.
The new Labour Party government has recently launched an NHS public consultation - to mixed responses. The Canary's Dr Julia ...
A long-term ME/CFS campaigner just launched a hospital care charter for ME – and it’s already taking off
Tuesday 29 October is an auspicious day for the myalgic encephalomyelitis (ME/CFS) community. Crucially, it marks three years to the ...
Rushed Off My Feet: a poem describes living with ME/CFS
Living with myalgic encephalomyelitis (ME/CFS) is physically devastating - but the social isolation that comes with it is often less ...
The NHS just sectioned a very severe ME/CFS patient under the Mental Health Act
NHS West Middlesex University Hospital has just placed very severe myalgic encephalomyelitis (ME/CFS) patient Carla Naoum under a Section 2 ...
Buried reports expose the DWP PIP process as a DISASTER for people with ME/CFS and EDS
A tranche of reports the Department for Work and Pensions (DWP) buried - including one for nearly two years - ...
Now severe ME/CFS patient Katiana has been forced onto a psych ward – by her parents
Abusive parents of a young woman in Greece who lives with severe ME/CFS have forced her onto a psychiatric ward ...
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