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 ...
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 34-year-old severe myalgic encephalomyelitis (ME/CFS) patient to a care home for pensioners. There, ...
A young woman, Nevra, who lives with severe myalgic encephalomyelitis (ME/CFS) is issuing an urgent call out for an in-person ...
Carla, a very severe myalgic encephalomyelitis (ME/CFS) patient has lost her appeal against West Middlesex hospital. Doctors sectioned Carla Naoum ...
The new Labour Party government has recently launched an NHS public consultation - to mixed responses. The Canary's Dr Julia ...
Tuesday 29 October is an auspicious day for the myalgic encephalomyelitis (ME/CFS) community. Crucially, it marks three years to the ...
Living with myalgic encephalomyelitis (ME/CFS) is physically devastating - but the social isolation that comes with it is often less ...
NHS West Middlesex University Hospital has just placed very severe myalgic encephalomyelitis (ME/CFS) patient Carla Naoum under a Section 2 ...
A tranche of reports the Department for Work and Pensions (DWP) buried - including one for nearly two years - ...
Abusive parents of a young woman in Greece who lives with severe ME/CFS have forced her onto a psychiatric ward ...
The Canary has been leaked a draft copy of the second NHS eLearning module on myalgic encephalomyelitis (ME/CFS). It comes ...
Every October, it's Dysautonomia Awareness Month: shedding light on a group of conditions that involve dysfunction of the autonomic nervous ...
On Friday 27 September, the last day of the Maeve Boothby O’Neill inquest, we heard that a much needed specialist ...
A former architecture student living with severe myalgic encephalomyelitis (ME/CFS) has created a series of 3D room scans to show ...
One of the biggest UK myalgic encephalomyelitis (ME/CFS) charities Action for ME (AFME) has been promoting a document pushing misinformation ...
Sally Callow is the founder of campaigning social enterprise ME Foggy Dog which raises funds for a chronic illness. Currently, ...
Historically, medicine has had a problem with women, especially those who were not married. Sounds unrealistic? The nineteenth century wasn’t ...
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