logo
MPs debate assisted dying before crunch parliament vote

MPs debate assisted dying before crunch parliament vote

Independent20-06-2025
Campaigners made last-ditch appeals outside parliament for and against assisted dying as MPs prepared for a crucial vote.
Legalisation could move a step closer for England and Wales depending on the result on Friday.
The outcome will lead to the Terminally Ill Adults (End of Life) Bill either clearing the House of Commons and moving to the Lords, or falling completely – with a warning the latter could mean the issue might not return to Westminster for a decade.
Opening her debate, Bill sponsor Kim Leadbeater, said her proposed legislation is 'cogent' and 'workable', with 'one simple thread running through it – the need to correct the profound injustices of the status quo and to offer a compassionate and safe choice to terminally ill people who want to make it'.
She shared emotional stories from people she had met throughout the campaign to legalise assisted dying, both bereaved and terminally ill.
Pressed by Conservative former minister Simon Hoare on concerns raised about the Bill by some doctors and medical bodies including the Royal College of Psychiatrists, Ms Leadbeater said: 'We have different views in this House and different people in different professions have different views.'
She noted that all the royal colleges have a neutral position on assisted dying.
The relatively narrow majority of 55 from the historic yes vote in November means every vote will count on Friday.
The Bill would fall if 28 MPs switched directly from voting yes to no, but only if all other MPs voted the same way as in November, including those who abstained.
Supporters and opponents of a change in the law gathered at Westminster early on Friday, holding placards saying 'Let us choose' and 'Don't make doctors killers'.
On the eve of the vote, in what will be seen as a blow to the Bill, four Labour MPs confirmed they will switch sides to oppose the proposed new law.
Paul Foster, Jonathan Hinder, Markus Campbell-Savours and Kanishka Narayan wrote to fellow MPs to voice concerns about the safety of the proposed legislation.
They branded it 'drastically weakened', citing the scrapping of the High Court judge safeguard as a key reason.
Conservative leader Kemi Badenoch urged her MPs to vote against the legislation, describing it as 'a bad Bill' despite being 'previously supportive of assisted suicide'.
As it stands, the proposed legislation would allow terminally ill adults in England and Wales with fewer than six months to live to apply for an assisted death, subject to approval by two doctors and a panel featuring a social worker, senior legal figure and psychiatrist.
Ms Leadbeater has insisted the replacement of High Court judge approval with multidisciplinary panels is a strengthening of the legislation, incorporating wider expert knowledge to assess assisted dying applications.
Before confirmation of the four vote-switchers, Ms Leadbeater acknowledged she expected 'some small movement in the middle' but that she did not 'anticipate that that majority would be heavily eroded'.
She insisted her Bill is 'the most robust piece of legislation in the world' and has argued that dying people must be given choice at the end of their lives in a conversation which has seen support from high-profile figures including Dame Esther Rantzen.
MPs have a free vote on the Bill, meaning they decide according to their conscience rather than along party lines.
There is no obligation on MPs to take part in the vote, and others present on Friday could formally abstain.
Ms Leadbeater warned that choosing not to support the assisted dying Bill is 'not a neutral act', but rather 'a vote for the status quo'.
She said: 'It fills me with despair to think MPs could be here in another 10 years' time hearing the same stories.'
All eyes will be on whether Prime Minister Sir Keir Starmer and senior colleagues continue their support for the Bill.
Sir Keir indicated earlier this week that he had not changed his mind since voting yes last year, saying his 'position is long-standing and well-known'.
Health Secretary Wes Streeting described Ms Leadbeater's work on the proposed legislation as 'extremely helpful', but confirmed in April that he still intended to vote against it.
Culture Secretary Lisa Nandy has voiced her continued backing of the Bill, saying she she hopes it can clear the Commons and continue its progress to becoming law.
She told Sky News she has a 'long-standing personal commitment to change the law on assisted dying with appropriate safeguards' and praised the 'very considered and respectful debate over the last few months on all sides'.
A vote must be called before 2.30pm, as per parliamentary procedure.
Friday's session began with considerations of outstanding amendments to the Bill, including one to prevent a person meeting the requirements for an assisted death 'solely as a result of voluntarily stopping eating or drinking'.
The amendment – accepted without the need for a vote – combined with existing safeguards in the Bill, would rule out people with eating disorders falling into its scope, Ms Leadbeater has said.
Another amendment, requiring ministers to report within a year of the Bill passing on how assisted dying could affect palliative care, was also approved by MPs.
Marie Curie welcomed the amendment, but warned that 'this will not on its own make the improvements needed to guarantee everyone is able to access the palliative care they need' and urged a palliative care strategy for England 'supported by a sustainable funding settlement – which puts palliative and end of life care at the heart of NHS priorities for the coming years'.
Ms Leadbeater has warned it could be a decade before legislation returns to Parliament if MPs reject her Bill on Friday.
A YouGov poll of 2,003 adults in Great Britain, surveyed last month and published on Thursday, suggested public support for the Bill remains at 73% – unchanged from November.
The proportion of people who feel assisted dying should be legal in principle has risen slightly, to 75% from 73% in November.
Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Healthy babies born in Britain after scientists used DNA from three people to avoid genetic disease
Healthy babies born in Britain after scientists used DNA from three people to avoid genetic disease

The Independent

time20 minutes ago

  • The Independent

Healthy babies born in Britain after scientists used DNA from three people to avoid genetic disease

Eight healthy babies were born in Britain with the help of an experimental technique that uses DNA from three people to help mothers avoid passing devastating rare diseases to their children, researchers reported Wednesday. Most DNA is found in the nucleus of our cells, and it's that genetic material — some inherited from mom, some from dad — that makes us who we are. But there's also some DNA outside of the cell's nucleus, in structures called mitochondria. Dangerous mutations there can cause a range of diseases in children that can lead to muscle weakness, seizures, developmental delays, major organ failure and death. Testing during the in vitro fertilization process can usually identify whether these mutations are present. But in rare cases, it's not clear. Researchers have been developing a technique that tries to avoid the problem by using the healthy mitochondria from a donor egg. They reported in 2023 that the first babies had been born using this method, where scientists take genetic material from the mother's egg or embryo, which is then transferred into a donor egg or embryo that has healthy mitochondria but the rest of its key DNA removed. The latest research 'marks an important milestone,' said Dr. Zev Williams, who directs the Columbia University Fertility Center and was not involved in the work. 'Expanding the range of reproductive options … will empower more couples to pursue safe and healthy pregnancies.' Using this method means the embryo has DNA from three people — from the mother's egg, the father's sperm and the donor's mitochondria — and it required a 2016 U.K. law change to approve it. It is also allowed in Australia but not in many other countries, including the U.S. Experts at Britain's Newcastle University and Monash University in Australia reported in the New England Journal of Medicine Wednesday that they performed the new technique in fertilized embryos from 22 patients, which resulted in eight babies that appear to be free of mitochondrial diseases. One woman is still pregnant. One of the eight babies born had slightly higher than expected levels of abnormal mitochondria, said Robin Lovell-Badge, a stem cell and developmental genetics scientist at the Francis Crick Institute who was not involved in the research. He said it was still not considered a high enough level to cause disease, but should be monitored as the baby develops. Dr. Andy Greenfield, a reproductive health expert at the University of Oxford, called the work 'a triumph of scientific innovation,' and said the method of exchanging mitochondria would only be used for a small number of women for whom other ways of avoiding passing on genetic diseases, like testing embryos at an early stage, was not effective. Lovell-Badge said the amount of DNA from the donor is insignificant, noting that any resulting child would have no traits from the woman who donated the healthy mitochondria. The genetic material from the donated egg makes up less than 1% of the baby born after this technique. 'If you had a bone marrow transplant from a donor … you will have much more DNA from another person,' he said. In the U.K., every couple seeking a baby born through donated mitochondria must be approved by the country's fertility regulator. As of this month, 35 patients have been authorized to undergo the technique. Critics have previously raised concerns, warning that it's impossible to know the impact these sorts of novel techniques might have on future generations. 'Currently, pronuclear transfer is not permitted for clinical use in the U.S., largely due to regulatory restrictions on techniques that result in heritable changes to the embryo," Williams, of Columbia, said in an email. 'Whether that will change remains uncertain and will depend on evolving scientific, ethical, and policy discussions." For about a decade, Congress has included provisions in annual funding bills banning the Food and Drug Administration from accepting applications for clinical research involving techniques, 'in which a human embryo is intentionally created or modified to include a heritable genetic modification.' But in countries where the technique is allowed, advocates say it could provide a promising alternative for some families. Liz Curtis, whose daughter Lily died of a mitochondrial disease in 2006, now works with other families affected by them. She said it was devastating to be told there was no treatment for her eight-month-old baby and that death was inevitable. She said the diagnosis 'turned our world upside down, and yet nobody could tell us very much about it, what it was or how it was going to affect Lily.' Curtis later founded the Lily Foundation in her daughter's name to raise awareness and support research into the disease, including the latest work done at Newcastle University. 'It's super exciting for families that don't have much hope in their lives,' Curtis said. ___ Ungar reported from Erie, Pennsylvania. ——- The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute's Department of Science Education and the Robert Wood Johnson Foundation. The AP is solely responsible for all content.

Eight babies born from pioneering IVF technique to prevent devastating disease
Eight babies born from pioneering IVF technique to prevent devastating disease

The Independent

time20 minutes ago

  • The Independent

Eight babies born from pioneering IVF technique to prevent devastating disease

Eight babies have been born in the UK thanks to a groundbreaking three-person IVF technique to prevent devastating disease, world-first data shows. Four boys and four girls, including one set of identical twins, have been delivered and are all doing well following treatment by a team in Newcastle, who pioneered the technique. One other woman is currently pregnant. The scientific method, known as mitochondrial donation treatment, is designed to prevent children from being born with devastating mitochondrial diseases that are passed down from their mothers. These illnesses can be fatal and often cause devastating damage to organs including the brain, muscle, liver, heart and kidney. Of the eight babies born, three are now aged under six months, two are aged six to 12 months, one is 12 to 18 months old, one is aged 18 to 24 months and one child is aged over two. All the babies are healthy and are meeting their milestones, according to the team from Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle University and Newcastle Fertility Centre. None of the eight babies shows signs of having mitochondrial DNA disease, which tends to affect around one in 5,000 births. The scientists said disease-causing mitochondrial DNA mutations, picked up in three of the children, are either undetectable or present at levels that are very unlikely to cause disease. The main lab method used by the team, known as pronuclear transfer (PNT), involves taking the egg from an affected mother, sperm from her partner and an egg from a donor who is free from disease. The mother of a baby girl born through mitochondrial donation said: 'As parents, all we ever wanted was to give our child a healthy start in life. 'Mitochondrial donation IVF made that possible. After years of uncertainty, this treatment gave us hope – and then it gave us our baby. 'We look at them now, full of life and possibility, and we're overwhelmed with gratitude. Science gave us a chance.' The mother of a baby boy added: 'We are now proud parents to a healthy baby, a true mitochondrial replacement success. This breakthrough has lifted the heavy cloud of fear that once loomed over us. 'Thanks to this incredible advancement and the support we received, our little family is complete. 'The emotional burden of mitochondrial disease has been lifted, and in its place is hope, joy, and deep gratitude.' Professor Sir Doug Turnbull, from Newcastle University and part of the team of researchers, said: 'Mitochondrial disease can have a devastating impact on families. 'Today's news offers fresh hope to many more women at risk of passing on this condition who now have the chance to have children growing up without this terrible disease.' In all the cases, the Newcastle team used the PNT technique after the egg was fertilised. For this, scientists transplanted the nuclear genome (which contains all the genes essential for a person's characteristics, such as hair colour and height) from the egg carrying the mitochondrial DNA mutation into an egg donated by an unaffected woman that had had its nuclear genome removed. Thanks to the procedure, the resulting baby inherits its parents' nuclear DNA, but the mitochondrial DNA is mainly inherited from the donated egg. Scientific progress in this area led Parliament to change the law in 2015 to permit mitochondrial donation treatment. Two years later, the Newcastle clinic became the first and only national centre licensed to perform it, with the first cases approved in 2018. Approval is given on a case-by-case basis by the UK's Human Fertilisation and Embryology Authority (HFEA). The new findings on the eight births, published in the New England Journal of Medicine, show that all the babies are developing normally. Aged 18 months, tests are carried out in areas such as gross motor skills, fine motor skills, cognitive and social development and language skills to check the babies are hitting milestones. The researchers will also check the children when they are aged five. Professor Bobby McFarland, director of the NHS Highly Specialised Service for Rare Mitochondrial Disorders at Newcastle Hospitals NHS Foundation Trust, said he was confident the children would carry on developing normally. He added: 'If we're not picking up subtle signs of problems at five, then we're really very clear that is not going to be a problem.' He added: 'In my work…I see children in intensive care units up and down this country and that's not pleasant. 'It's very difficult for families to deal with these diseases, they are devastating… 'To see babies born at the end of this is just amazing really.' Mary Herbert, professor of reproductive biology at Newcastle University, added: 'PNT happens in the small hours of the morning – those long nights. And it has paid off. 'It's fair to say it's rewarding. In science though, periods of joy are fleeting and brief because you're always thinking what is the next challenge? How do we optimise it further?' She said the slight DNA mutations seen in three of the children are 'way, way below the threshold that would cause disease'. Peter Thompson, chief executive of the HFEA, said: 'Ten years ago, the UK was the first country in the world to licence mitochondrial donation treatment to avoid passing the condition to children. 'For the first time, families with severe inherited mitochondrial illness have the possibility of a healthy child. 'Although it's still early days, it is wonderful news that mitochondrial donation treatment has led to eight babies being born. 'Only people who are at a very high risk of passing a serious mitochondrial disease onto their children are eligible for this treatment in the UK, and every application for mitochondrial donation treatment is individually assessed in accordance with the law.' Dr Andy Greenfield, from the University of Oxford, said: 'It is a triumph of scientific innovation in the IVF clinic – a world-first that shows that the UK is an excellent environment in which to push boundaries in IVF; a tour de force by the embryologists who painstakingly developed and optimised the micromanipulation methods; an example of the value of clinical expertise, developed over decades of working with children and adults suffering from these devastating diseases, being used to support a new intervention and subsequent follow-up, potentially for many years.' Beth Thompson, executive director for policy and partnerships at Wellcome, said: 'This is a remarkable scientific achievement, which has been years in the making. 'The pioneering work behind mitochondrial donation is a powerful example of how discovery research can change lives.' Professor Dagan Wells, from the University of Oxford, said the study showed established methods for avoiding mitochondrial DNA diseases, such as preimplantation genetic testing, perform well and will be suitable for most women at risk of having an affected child. 'A minority of patients are unable to produce any embryos free of mitochondrial disease, and for those women the study provides hope that they may be able to have healthy children in the future,' he added.

BBC's refusal to properly describe Hamas stems from its institutional anti-Israel bias
BBC's refusal to properly describe Hamas stems from its institutional anti-Israel bias

The Sun

time20 minutes ago

  • The Sun

BBC's refusal to properly describe Hamas stems from its institutional anti-Israel bias

Beeb's bias EVEN after a run of avoidable scandals, senior BBC execs still don't get it. Yesterday they were dancing on the head of a pin over accepted editorial breaches in its Gaza documentary. 2 Viewers weren't told of any links between a 13-year-old Palestinian child narrator and his Hamas father. But in a video to all staff, the BBC claims the dad was only a member of the 'political wing'. Except it is British government policy that no such distinction exists. And to normal people outside Auntie's bubble, Hamas members are ALL terrorists. The BBC's refusal to properly describe those responsible for the October 7 massacre stems from its seemingly unending institutional anti-Israel bias. Viewers deserve the truth, not squirming excuses. Prevent what? THE Government's anti-terror Prevent strategy already focuses too much on tackling far-right terrorism — despite Islamists posing a greater threat. Now a report says it is also failing to deal with suspects fixated on violence because their views don't fit into any recognised terror ideology. 2 Southport monster Axel Rudakubana had repeatedly searched online for shootings, terror attacks and Gaza war videos. But despite three referrals, Prevent did nothing because he wasn't deemed a terrorist. Three little girls died. Ali Harbi Ali, who murdered MP David Amess, was let go after one session and described as a 'great person.' Those obsessed with extreme violence shouldn't need an ideological label attached to them before they're stopped. The clue to Prevent's role is in its name. Keep It Down WE hope the Chancellor took note of the fact that the painful inflation spike was caused in part by rising fuel prices. It's why Rachel Reeves should rule out any idea of ending the fuel duty freeze. That would only clobber the hard-working people the Government insists it wants to protect. The Sun's 15-year Keep It Down campaign has saved Brits almost £100billion which has been ploughed back into the economy by grateful motorists. Helping drivers also helps to drive growth, Chancellor. Whip round WE welcome Keir Starmer getting tough and suspending self-indulgent leftie MP s. It's just a pity he didn't act before their fantasy student politics derailed welfare reforms and cost the country £5billion. That dithering means we all now face paying more tax.

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