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 ...
Tag: ME/CFS
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 ...
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 ...
Rushed Off My Feet: a poem describes living with ME/CFS
Living with myalgic encephalomyelitis (ME/CFS) is physically devastating - but ...
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 ...
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 ...
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 ...
The Canary has a leaked copy of the second NHS eLearning module on ME/CFS. It’s not good.
The Canary has been leaked a draft copy of the ...
It’s Dysautonomia Awareness Month – but we need to talk about EDS and ME/CFS
Every October, it's Dysautonomia Awareness Month: shedding light on a ...
Through the fog: toxic empathy and medical apathy in long Covid and ME/CFS
On Friday 27 September, the last day of the Maeve ...
3D room scans show the harrowing reality of life with severe ME, trapped in a neglectful household
A former architecture student living with severe myalgic encephalomyelitis (ME/CFS) ...
An ME/CFS charity has just shamed itself again. So why do people still support it?
One of the biggest UK myalgic encephalomyelitis (ME/CFS) charities Action ...
Paralympics under fire for #EveryBodyMoves campaign – that EXCLUDES millions of disabled people
Sally Callow is the founder of campaigning social enterprise ME ...
Phantom healthcare for ‘real’ diseases: when will ME/CFS and long Covid get parity?
Historically, medicine has had a problem with women, especially those ...
Grieving for loss of life: the untold ME/CFS – from silent, darkened rooms
In silent darkened rooms where millions lie, the world turns ...
It’s Gastroparesis Awareness Month – yet we need to talk about EDS and ME/CFS
August is Gastroparesis Awareness Month. However, two conditions gastroparesis is ...
Maeve’s inquest was a whitewash and the coroner betrayed everyone living with ME/CFS
On Friday 9 August, the inquest into the death of ...
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