logo
'I could live 30 years - but want to die': Has assisted dying in Canada gone too far?

'I could live 30 years - but want to die': Has assisted dying in Canada gone too far?

BBC News04-04-2025
April Hubbard sits on the theatre stage where she plans to die later this year.She is not terminally ill, but the 39-year-old performance and burlesque artist has been approved for assisted dying under Canada's increasingly liberal laws.Warning: This article contains details and descriptions some readers may find disturbingShe is speaking to BBC News from the Bus Stop Theatre, an intimate auditorium with a little under 100 seats, in the eastern city of Halifax, Nova Scotia.Illuminated by a single spotlight on a stage she has performed on many times before, she tells me she plans to die here "within months" of her imminent 40th birthday. She'll be joined by a small group of her family and friends.April plans to be in a "big comfy bed" for what she calls a "celebratory" moment when a medical professional will inject a lethal dose into her bloodstream."I want to be surrounded by the people I love and just have everybody hold me in a giant cuddle puddle and get to take my last breath, surrounded by love and support," she says.April was born with spina bifida and was later diagnosed with tumours at the base of her spine which she says have left her in constant, debilitating pain.
She's been taking strong opioid painkillers for more than 20 years and applied for Medical Assistance in Dying (Maid) in March 2023. While she could yet live for decades with her condition, she qualified to end her life early seven months after applying. For those who are terminally ill it is possible to get approval within 24 hours."My suffering and pain are increasing and I don't have the quality of life anymore that makes me happy and fulfilled," April says. Every time she moves or breathes, she says it feels like the tissues from the base of her spine "are being pulled like a rubber band that stretches too far", and that her lower limbs leave her in agony.We meet April as, almost 3,000 miles away, MPs are scrutinising proposals to legalise assisted dying in England and Wales. They voted in principle in support of those plans in November 2024, but months of detailed scrutiny have followed - and further votes in the Commons and Lords are required before the bill could possibly become law.This week, the BBC witnessed a man's death in California, where assisted dying laws are far more similar to those being considered in Westminster.Critics say Canada is an example of the "slippery slope", meaning that once you pass an assisted dying law it will inevitably widen its scope and have fewer safeguards.Canada now has one of the most liberal systems of assisted dying in the world, similar to that operating in the Netherlands and Belgium. It introduced Maid in 2016, initially for terminally ill adults with a serious and incurable physical illness, which causes intolerable suffering. In 2021, the need to be terminally ill was removed, and in two years' time, the Canadian government plans to open Maid to adults solely with a mental illness and no physical ailment.Opponents of Maid tell us that death is coming to be seen as a standard treatment option for those with disabilities and complex medical problems."It is easier in Canada to get medical assistance in dying than it is to get government support to live," says Andrew Gurza, a disability awareness consultant and friend of April's.Andrew, who has cerebral palsy and uses a wheelchair, says he respects April's decision, but tells us: "If my disability declines and my care needs got higher, I'd still want to be here. To know there's a law that's saying you could easily end your life - it's just really scary."
Before she was approved for Maid, April was assessed by two independent physicians who were required to inform her of ways to alleviate her suffering and offer alternative treatments."The safeguards are there," she says, when we press her about disabled people who feel threatened by assisted dying, or whether Maid is being used as a shortcut to better quality care. "If it's not right for you and you're not leading the charge and choosing Maid, you're not going to be able to access it unless it's for the right reasons," she adds.There were 15,343 Maid deaths in 2023, representing around one in 20 of all deaths in Canada - a proportion that has increased dramatically since 2016 and is one of the highest in the world. The average age of recipients was 77.In all but a handful of cases, the lethal dose was delivered by a doctor or nurse, which is also known as voluntary euthanasia. One doctor we spoke to, Eric Thomas, said he had helped 577 patients to die.
Dr Konia Trouton, president of the Canadian Association of Maid Assessors and Providers, has also helped hundreds of patients to die since the law was introduced.The procedure is the same each time - she arrives at the home of the person who has been given approval for Maid and asks if they wish to go ahead with it that day. She says the patients always direct the process and then give her the "heads up and ready to go"."That gives me an honour and a duty and a privilege to be able to help them in those last moments with their family around them, with those who love them around them and to know that they've made that decision thoughtfully, carefully and thoroughly," she adds. If the answer is yes, she opens her medical bag.Demonstrating to the BBC what happens next, Dr Trouton briefly puts a tourniquet on my arm. She shows me where the needle would be inserted into a vein in the back of my hand to allow an intravenous infusion of lethal drugs.In her medical bag she also has a stethoscope. "Strangely, these days I use it more to determine if someone has no heartbeat rather than if they do," she tells me.A list of organisations in the UK offering support and information with some of the issues in this story is available at BBC Action Line
Some 96% of Maid provisions are under "track one" where death is "reasonably foreseeable". Dr Trouton says that means patients are on a "trajectory toward death", which might range from someone who has rapidly spreading cancer and only weeks to live or another with Alzheimer's "who might have five to seven years".The other 4% of Maid deaths come under "track two". These are adults, like April, who are not dying but have suffering which is intolerable to them from a "grievous and irremediable medical condition".That is in stark contrast to Labour MP Kim Leadbeater's bill to legalise assisted dying in England and Wales, which says patients must be expected to die within six months. The Westminster bill would not allow doctors to give a lethal dose – rather patients would have to self-administer the drugs, usually by swallowing them.Death via intravenous infusion normally takes just a few minutes, as the lethal drugs go straight into the bloodstream, whereas swallowing the drugs means patients usually take around an hour or two to die, but can take considerably longer, although they are usually unconscious after a few minutes.Dr Trouton told me she regarded the Canadian system as quicker and more effective, as do other Maid providers. "I'm concerned that if some people can't swallow because of their disease process, and if they're not able to take the entire quantity of medication because of breathing difficulties or swallowing difficulties, what will happen?"
'Canada has fallen off a cliff'
But opponents argue it's being used as a cheaper alternative to providing adequate social or medical support.One of them is Dr Ramona Coelho, a GP in London, Ontario, whose practice serves many marginalised groups and those struggling to get medical and social support. She's part of a Maid Death Review Committee, alongside Dr Trouton, which examines cases in the province.Dr Coelho told me that Maid was "out of control". "I wouldn't even call it a slippery slope," she says "Canada has fallen off a cliff."
"When people have suicidal ideations, we used to meet them with counselling and care, and for people with terminal illness and other diseases we could mitigate that suffering and help them have a better life," she says. "Yet now we are seeing that as an appropriate request to die and ending their lives very quickly."While at Dr Coelho's surgery I was introduced to Vicki Whelan, a retired nurse whose mum Sharon Scribner died in April 2023 of lung cancer, aged 81. Vicki told me that in her mum's final days in hospital she was repeatedly offered the option of Maid by medical staff, describing it as like a "sales pitch".The family, who are Catholic, discharged their mother so she could die at home, where Vicki says her mum had a "beautiful, peaceful death". "It makes us think that we can't endure, and we can't suffer a little bit, and that somehow now they've decided that dying needs to be assisted, where we've been dying for years."All of a sudden now we're telling people that this is a better option. This is an easy way out and I think it's just robbing people of hope."
'Not a way I want to live'
So is Canada an example of the so-called slippery slope? It's certainly true that the eligibility criteria has broadened dramatically since the law was introduced nine years ago, so for critics the answer would be an emphatic yes and serve as a warning to Britain.Canada's assisted dying laws were driven by court rulings. Its Supreme Court instructed Parliament that a prohibition on assisted dying breached the country's Charter of Rights and Freedoms. The extension of eligibility for those who were not terminally ill was in part a response to another court decision.In Britain, judges in the most senior courts have repeatedly said any potential change to the law around assisted dying is a matter for Parliament, after the likes of Tony Nicklinson, Diane Pretty and Noel Conway brought cases arguing the blanket ban on assisted suicide breached their human rights.April knows some people may look at her, a young woman, and wonder why she would die."We're the masters of masking and not letting people see that we're suffering," she says. "But in reality, there's days that I just can't hide it, and there's many days where I can't lift my head off the pillow and I can't eat anymore."It's not a way I want to live for another 10 or 20 or 30 years."Additional reporting by Joshua Falcon.
Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

'I forgot a name at work - I thought it was menopause'
'I forgot a name at work - I thought it was menopause'

Daily Record

time3 days ago

  • Daily Record

'I forgot a name at work - I thought it was menopause'

April Tate, 52, first noticed something was wrong when she forgot a child's name while working as a childminder A woman who believed her memory lapses were down to the menopause received the shocking news that she had an inoperable brain tumour. April Tate, 52, first realised something wasn't right when she couldn't remember a child's name whilst working as a childminder. ‌ Thinking it was simply part of the menopause, she brought it up during a routine GP telephone consultation, only to be told to come to the surgery straight away. A scan at Victoria Hospital, Kirkcaldy, quickly revealed a growth on her brain. ‌ Medical experts diagnosed her with a posterior falcine meningioma - a low-grade tumour situated deep within the centre of her brain. Because of where it was located, an operation was deemed too risky. ‌ April, a single mum to daughter Abby, was put on a watch and wait programme, with regular scans every six months. The tumour was initially slow growing, but in late 2022, medics discovered it had grown larger. She received stereotactic radiotherapy, a precise treatment that reduces harm to surrounding brain tissue, and subsequent scans have shown ongoing shrinkage. Now, April has gone back to work, started running, and is taking part in the 88 Squats a Day in July challenge for Brain Tumour Research to boost awareness and raise money. April, from Burntisland, Fife, said: "When they said I had a brain tumour, my first thought was that I was going to die. Being self-employed meant taking time off for treatment brought financial pressure too, which just added to the stress." ‌ April's symptoms started gradually. In 2018, she experienced a lapse in memory whilst at work. Worried, she mentioned it to her GP, who swiftly referred her onwards. A scan at Victoria Hospital revealed the presence of a tumour. April said: "It was a numbing moment. I was a single mum, and my daughter Abby was still a teenager. All I could think about was not being there for her." ‌ The tumour's position meant an operation wasn't possible. She said: "When the surgeon explained the tumour was located in a really difficult part of my brain and he'd only attempted surgery in that area once before, it was a difficult truth to accept." Instead, April was put on a schedule of routine scans. She said: "It was terrifying to live with the unknown of whether it would grow or not. Over time, I began to adjust. The tumour was slow-growing, and for a while, it didn't change much." However, by late 2022, the tumour had expanded. It remained below 30mm, which meant April was eligible for stereotactic radiotherapy. The procedure, whilst accurate, was demanding. ‌ "The radiotherapy itself was fairly quick each day, but it was exhausting," she said. "The team had to make a custom mask to keep my head completely still, which felt claustrophobic and intense. I just closed my eyes, listened to music and tried to stay calm. The hardest part came afterwards, with having to wait to find out if it had worked." To her immense relief, the tumour had diminished in size. Subsequent scans revealed continued shrinkage, with April now undergoing yearly check-ups. She has successfully returned to employment and even accomplished her debut 5k race earlier this year. Driven to create change, April is undertaking the 88 Squats a Day in July challenge, backing Brain Tumour Research. ‌ The initiative seeks to generate £2,740 – the sum required to finance one day of research at the Scottish Brain Tumour Research Centre of Excellence, working alongside Beatson Cancer Charity. "People hear the words 'benign' or 'low-grade' and assume it's nothing serious, but I still live with this every day," April said. "There's something in my brain that shouldn't be there, and it could change at any time. "I even worried about how it might affect new relationships and not wanting to burden someone else with what I was going through. But we still deserve to live fully, and to love and be loved. "What shocks me most is how little funding goes into researching brain tumours. That has to change." Ashley McWilliams, community development manager at Brain Tumour Research, said: "April's story is a powerful reminder that brain tumours can be easily missed or mistaken for everyday health issues. Her strength in facing such a frightening diagnosis, and her commitment to raising awareness, is incredibly inspiring."

People in Gaza are 'walking corpses' - with one in five children malnourished, says UN
People in Gaza are 'walking corpses' - with one in five children malnourished, says UN

Sky News

time3 days ago

  • Sky News

People in Gaza are 'walking corpses' - with one in five children malnourished, says UN

A fifth of the children in Gaza City are malnourished and more than 100 people, most of them youngsters, have reportedly died of hunger there, the UN has said. Philippe Lazzarini, the commissioner-general of the UN Relief and Works Agency (UNRWA), quoting a colleague, said on Thursday that people in Gaza, where the supply and distribution of aid is controlled by Israel, "are neither dead nor alive, they are walking corpses". Most of the youngsters the agency sees are "emaciated, weak and at high risk of dying if they don't get the treatment they urgently need. "This deepening crisis is affecting everyone, including those trying to save lives in the war-torn enclave." UNRWA's frontline health workers are surviving on "one small meal a day, often just lentils, if at all. They are increasingly fainting from hunger while at work", Mr Lazzirini said. "When caretakers cannot find enough to eat, the entire humanitarian system is collapsing." Israel to allow journalists to move freely in and out of Gaza amid fears reporters there are facing the risk of starvation. BBC News, Agence France Press, Associated Press and Reuters said in a statement published on Thursday they are "desperately concerned for our journalists in Gaza, who are increasingly unable to feed themselves and their families. They said: "For many months, these independent journalists have been the world's eyes and ears on the ground in Gaza. They are now facing the same dire circumstances as those they are covering. "Journalists endure many deprivations and hardships in war zones. We are deeply alarmed that the threat of starvation is now one of them. "We once again urge the Israeli authorities to allow journalists in and out of Gaza. It is essential that adequate food supplies reach the people there." Israeli government spokesperson David Mencer told Sky News that food shortages have "been engineered by Hamas", and that there "is no famine in Gaza". 2:00 Speaking on Wednesday's News Hour with Mark Austin, Mr Mencer said aid is "flowing" into the enclave but Hamas "loots the trucks [and] deliberately endangers its own people". The fighters deny stealing food. More than 4,400 aid trucks have been allowed into Gaza since Israel lifted its blockade in May, roughly 70 trucks a day, which is the lowest rate of the war and far below the 500-600 trucks a day the UN says is needed. "The problem is not Israel," he said. "The problem is Hamas." The UK and several other countries have condemned the current aid delivery model, known as the Gaza Humanitarian Foundation, which is backed by the Israeli and American governments. It has reportedly resulted in Israeli troops firing on Palestinian civilians in search of food on multiple occasions. More than 800 people have reportedly been killed in recent weeks trying to reach food, mostly in shootings by Israeli soldiers posted near distribution centres.

Edinburgh South West MP's bill progresses
Edinburgh South West MP's bill progresses

Edinburgh Reporter

time6 days ago

  • Edinburgh Reporter

Edinburgh South West MP's bill progresses

A bill to highlight the need for research into cancers which are designated 'rare', and which was introduced by Dr Scott Arthur, MP for Edinburgh South West, has now progressed to the House of Lords. A first reading of the Rare Cancers Bill has already been heard in the Lords, it is expected to returns there in the autumn for its second reading. The purpose of the new law is to 'make provision to incentivise, research and investment into the treatment of rare types of cancer'. These are the group of cancers in respect of which little progress has been made in researching treatment or a cure. The Rare Cancers Bill is what is known as a ballot bill – a type of Private Members' Bill used in the House of Commons. Around ten months ago Dr Arthur was chosen to pick a numbered ping pong ball out of a goldfish bowl at the start of the parliamentary term to give him the chance of proposing a Ballot Bill. He was then able to choose his own subject matter. Dr Arthur said: 'It feels like things are lining up. The vast bulk of these bills do fail, so it's tremendous to get this far. And let's hope it doesn't fail, but what it's done so far is it's really got people talking about rare cancers, and it's really put some of the charities which support this sector in the spotlight, and it's been a chance for them to connect with people as well.' He continued: 'What got me started on this was that my father-in-law died of a type of brain tumour called glioblastoma, which is a rare cancer type. It wasn't until I drew the ballot and people started to contact me about what I could focus my bill on that I found that the type of brain tumour he died from – there's been no real progress in terms of treatment for decades. 'And what happened to him, he died around six months after a diagnosis. That is not unusual. I think on average, glioblastoma, nine months. Some people do live significantly longer than that, particularly if they manage to get surgery. But nine months is the average life expectancy after diagnosis. And it's the same for a lot of cancers in this field where there's just not been the progress. 'I spoke to the father of a preschool child, she had neuroblastoma, which is a type of cancer which attaches itself to your internal organs, and she died. And again, same story, he found out there's just so little money going into researching that cancer type and just not enough progress. And people in Edinburgh will remember Kira the Machine, the teenager, she had the same type of cancer and she's been able to access trials and cutting edge treatments, but still 10 years on, she still has the cancer and it's still a big part of her life.' 'The bill has the backing of around 40 charities which was useful as the bill came to the House of Commons for its Third Reading to be met with many amendments from fellow MP Sir Christopher Chope. The charities sent 120,000 emails to their supporters and some contacted their own MPs which meant the bill had a lot of support to get through the Commons. 'I think I've said this many times, I've always felt it was better to come away with something rather than nothing. Some of the private members bills, what MPs do, because they know how difficult it can be to succeed. What they do is they aim really high and they create a fantastic campaign because it's about raising awareness and they accept that ultimately there's a good chance it's not going to succeed. But our focus is on succeeding and actually delivering something.' His parliamentary colleague Tracy Gilbert also secured a Ballot Bill – hers was a different topic completely – the Absent Voting (Elections in Scotland and Wales) Bill, and that has also passed to the House of Lords for a Second Reading. Third Reading Dr Arthur said in the House of Commons during the Third Reading that when he was successful in having his bill supported he got 'so many emails, many of which were about glioblastoma. The reality is that someone who was diagnosed that day with glioblastoma would more than likely be dead by now – that is how serious the condition is'. The Edinburgh South West MP has used the parliamentary time to mention several constituents who have or have had a rare cancer. He said: 'I shared the tragic stories of a young constituent called Tilly, who passed away from neuroblastoma, and Kira, who has lived with the same condition for a decade—half of her life. I am proud to wear the Solving Kids' Cancer badge, which Kira's mother Aud gave me when I last met her. 'One lady travelled quite far to meet me at my constituency surgery in July in Tesco in Colinton Mains. Her daughter was diagnosed with a sarcoma. In Tesco, next to the bleeping self-checkout aisles, she told me about the uncertainty she had faced after that diagnosis and how she had found it impossible even to understand which trials were available, let alone access them. I could see that she had felt powerless and had lost hope. The other reason she was in Edinburgh – perhaps the most important reason – was that she was meeting her ex-husband to scatter her daughter's ashes in a local park. What is happening to people who face these conditions is quite incredible, so it is right that we seek to address them.' He explained to the House that there are three recurring themes in all the stories he has heard – the first is frustration, the second is perseverance and the third is that every story concludes with an offer of help from those patients who 'know that their options are limited'. Dr Arthur said: 'For far too long, rare cancer patients have been left behind—as medical science makes significant progress in many other complex fields, we have not seen enough progress in this one—but they feel this piece of legislation could mark a meaningful shift for many and turn out to be life-altering, perhaps even lifesaving, for some. There is one statistic that I often mention: rare cancers are not really rare, as they account for 47% of all cancer diagnoses in the UK each year. That equates to 180,000 people. If you are one of those 47%, two things are true: you are more likely to face outdated treatments and you are more likely to die.' The bill should spark a government review of what are known as 'orphan drugs' – a term which Dr Arthur says he prefers to talk about rare conditions – to explore new ways of getting the drugs companies to try to find innovative treatments for rare cancers. He hopes this will reduce barriers to research and also mean more trials are conducted in the UK, so saving more lives. Dr Scott Arthur MP (Edinburgh South West, Labour) presenting his bill to the Speaker in October 2024. Dr Scott Arthur MP (Edinburgh South West, Labour) PHOTO © House of Commons Like this: Like Related

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into a world of global content with local flavor? Download Daily8 app today from your preferred app store and start exploring.
app-storeplay-store