
EXCLUSIVE I've been trapped in a hospital for NINE YEARS and staff tell me the way out is killing myself
A disabled Canadian man has told the Daily Mail about his living hell of nine years in a hospital where he says caregivers badger him to end his life by lethal injection.
Roger Foley is stuck in a room in the London Health Sciences Centre (LHSC) in London, Ontario, where staff repeatedly drop hints about euthanasia, he says.

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Daily Mail
24 minutes ago
- Daily Mail
After five failed rounds of IVF, my partner died. I thought I'd go mad with grief... instead I took the most desperate measure and used his sperm to father the children I longed for: CHARLOTTE CRIPPS
At the time it felt like any other Tuesday morning in our two-bedroom home in Notting Hill, west London, but I can remember it all now with precise vividness. I was rushing around getting ready for my day's work as a journalist. Alex, my 48-year-old partner of ten years, was sitting on the bed scrolling through emails while our 12-week-old golden retriever puppy chewed on a chair leg. There was a peculiar smell. I was boiling some herbs in a heart-shaped Le Creuset dish on the stove – a special concoction from my Chinese acupuncturist. I was 40 and preparing for another IVF cycle (this would be our sixth attempt – we'd been trying for a baby for three years) and the drink was supposed to improve my fertility.


The Guardian
an hour ago
- The Guardian
SBS's Insight accused of betraying people living with chronic fatigue syndrome who appeared on program
People living with chronic fatigue syndrome who appeared on SBS's Insight program have accused the broadcaster of betraying them in the final cut, which presented what they claim is a potentially harmful and unscientific narrative and favoured a person who said she had 'cured herself' by 'listening to her body'. The SBS ombudsman is investigating their individual complaints, as well as one from Emerge Australia, the national advocacy body for patients with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). There are hundreds of negative comments about the episode on the program's social media pages. One participant who is a carer for his wife and daughter, Peter McCluskey, has told the SBS ombudsman the final broadcast 'compounded the invalidation and gaslighting that patients and carers endure daily'. McCluskey wrote a first-person piece for SBS about his family's experience, which was published ahead of the episode airing last month. 'The editorial decisions made by Insight undermined what we naively thought was the very purpose of the episode and breached multiple clauses of the SBS code of practice,' he wrote in a complaint seen by Guardian Australia. He accused SBS of '… sidelining science, clinical expertise, and the lived experience of patients – all under the guise of balance'. 'Rather than giving voice to a stigmatised and misunderstood community, the program re-traumatised it.' Sign up to get Guardian Australia's weekly media diary as a free newsletter The chief executive of Emerge Australia, Anne Wilson, accused SBS of presenting what she described as 'a harmful narrative' by giving disproportionate airtime to one person who said she had recovered from ME/CFS, and then to have contracted and recovered from rheumatoid arthritis without medical care. She said she had 'cured herself' by 'listening to her body' and was now running marathons. Wilson accused Insight of undermining decades of scientific research, education and advocacy by not challenging the narrative. 'Scientific evidence states that there is no recovery from rheumatoid arthritis and less than 10% of people with ME/CFS return to pre-illness functioning,' Wilson said. 'Of further concern, this person claimed their recovery was due to attitude alone, implying that recovery is a choice or can be achieved through effort alone. There are no proven treatments for ME/CFS and there is no cure. The small number who recover are the lucky few.' Emerge was approached by Insight producers to provide people to appear on the show and agreed to because of the program's 'positive reputation as well-researched, serious journalism', Wilson said. 'We were pleased the program chose to feature the often-overlooked challenges of living with invisible illnesses such as ME/CFS, long Covid, fibromyalgia and similar conditions. Sign up to Weekly Beast Amanda Meade's weekly diary on the latest in Australian media, free every Friday after newsletter promotion 'We were, however, extremely disappointed by the unbalanced narrative portrayed in the episode. Ironically, the episode accurately reflected the gaslighting experienced by many living with invisible illnesses.' Another participant, Allie Rawlings, said she agreed to be part of the studio discussion because she believed SBS had integrity, but she was disappointed with the edited program which was broadcast. 'The content aired bore little resemblance to the contributions I made during filming, stripping away the nuance, complexity, and intent of my perspective,' she told the ombudsman. Another complainant, Lauren Beasley, said she had hoped the episode would bring clarity and compassion about her illness to the wider public. 'Instead of platforming the full spectrum of experiences, the episode centred disproportionately on a highly individualised recovery narrative – one based on mindset, willpower, and personal agency,' Beasley wrote. A spokesperson for SBS said Insight's remit is to examine topical issues from a variety of perspectives. 'We generally receive a range of feedback, as we did for this topic, and we'll be responding to these audience members in line with our usual practices,' the spokesperson said. 'Like all of our content, Insight is subject to the SBS Code of Practice, which states that SBS will share a diversity of views and perspectives, and requires our news and current affairs programs to provide balanced and impartial coverage. We appreciate the contribution of the participants who shared their lived experiences in the studio and helped to raise awareness of the important issue of invisible illness.'


Daily Mail
an hour ago
- Daily Mail
Calls for one MILLION more blood donors as stocks drop dangerously low after reserves struggled to recover in wake of NHS cyber attack: How you can help
The NHS needs one million more blood donors following the cyber attack that crippled it's supply, officials have said. Low blood stocks prompted officials to issue an 'amber alert' over supply for hospitals last year and NHS Blood and Transplant (NHSBT) said that more must be done to avoid a 'red alert', which means that blood supply is so low that there is a threat to public safety. Officials described the last year as 'challenging' for blood stocks, highlighting how just two per cent of the population keep the nation's blood stocks afloat. This means just under 800,000 people sustained the whole of England's blood supply over the past 12 months and NHSBT said one million donors are needed to meet demand. NHSBT said that there has been a rise in the number of people who registered to be donors in the last year, but only 24 per cent of these have gone on to donate. The amber alert was triggered in July 2024 after a cyber attack on London hospitals. And blood stocks have remained low ever since, officials said. It said there is a 'critical' need for more donors who have the so-called universal blood type - O negative blood - which is needed for treatment in emergencies. There is also a need for more black donors, who are more likely to have specific blood types which can help treat people with sickle cell disease. NHSBT chief executive Dr Jo Farrar said: 'There are many thousands of people who donate regularly and help us keep patients alive. Thank you. You are amazing. You keep the NHS going and save and transform thousands of lives a year. 'Our stocks over the past 12 months have been challenging. If we had a million regular donors, this would help keep our stocks healthy - you'd truly be one in a million. 'Please book an appointment today, experience how good it feels to save lives, and come and do it again in a few months.' Two thirds of the blood collected is used to treat people who rely on blood transfusions including people with cancer and those with blood conditions. One family is backing the campaign for more donors due to their own experience receiving regular blood transfusions. Four-year-old Isaac Balmer, from Hull, was born with hereditary spherocytosis - a genetic blood condition which causes red blood cells to break down faster than normal, leading to severe anaemia and other complications. He receives blood transfusions every 12 weeks. His mother Jasmin Suggit, a newborn hearing scanner at the hospital where Isaac receives his treatment, said: 'It's been a rollercoaster; Isaac's haemoglobin levels fluctuate, and when they drop significantly, he becomes lethargic and jaundiced. 'But when he receives his transfusion, you see the colour return to his cheeks, and his energy levels soar before our eyes. It is incredible. 'During his transfusions, he refers to donor blood as 'Hulk blood' and imagines himself becoming stronger and healthier, but this wouldn't be possible without the real life, everyday superheroes who keep Isaac and others like him alive, thanks to their regular blood donations.' Health Minister Baroness Merron said: 'The NHS is in urgent need of more lifesaving blood donors from all backgrounds. We are working alongside NHS Blood and Transplant to make donating blood easier than ever before, opening up new donor centres and making appointments available closer to home.'