Showing posts sorted by date for query bill 11. Sort by relevance Show all posts
Showing posts sorted by date for query bill 11. Sort by relevance Show all posts

Wednesday, October 7, 2026

Bill C-218 was defeated. What will happen next?

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

Alex Schadenberg
It is too early to assess what will happen now that Bill C-218, the private members bill that was sponsored by Tamara Jansen (MP) was defeated in parliament by a vote of 187 to 141 on October 7. 

Bill C-218 would have amended the Criminal Code to prevent euthanasia for mental illness as a sole criteria.

The defeat of Bill C-218 was directly related to the announcement, the same day, at 12 noon by Justice Minister Sean Fraser and Health Minister Marjorie Michel. They stating that the federal government will introduce legislation, this fall, that will prevent the implementation of euthanasia for mental illness as a sole criteria. However, the government legislation will also permit euthanasia by advanced request.

Euthanasia by advanced request is a very dangerous concept as it would permit doctors and nurse practitioners to kill someone who has become incompetent, based on an advanced request. 

We knew that the language of Bill C-218 would have prevented euthanasia for mental illness, as a sole criteria, but we have not seen the language of the upcoming government bill. 

Language is everything. 

Who would make the final decision to poison an incompetent person to death?

The government bill, that we have not seen, may create a catch 22 situation where voting "No" to the bill would allow euthanasia for mental illness, as a sole criteria, but voting "Yes" to the bill would permit euthanasia by advanced request.

The government should separate the issues with two bills instead of one.

Until we analyse the language of the bill, we will not determine whether the government bill will actually prevent euthanasia for mental illness as a sole criteria.

Press Conference on October 7 at 11 am 

October 7 Press Conference
Dr Laurence Normand-Rivest, a family physician in Montréal who cares for geriatric patients and provides in-home palliative care, Dr Paul Saba a family physician in Lachine Québec who has personal experience with caring for people with mental health related trauma, Odile Marcotte, a retired professor from the Université du Québec à Montréal and a former deputy director of the Centre de recherches mathématiques, and a EPC Board member, and Alex Schadenberg, Executive Director of the Euthanasia Prevention Coalition spoke at a Press Conference.

Dr Normand-Rivest, Dr Saba, Marcotte and Schadenberg witnessed the historic and dissappointing vote on Bill C-218, at 3:30 pm in the parliamentary gallery.

Monday, October 5, 2026

EPC Press Conference: Vote YES on Bill C-218


Media Advisory (Link to Media Advisory)

Alex Schadenberg
Bill C-218, the bill to prevent MAiD for Mental Illness as a sole criteria, will go to a vote on October 7.

EPC Press Conference: Wednesday, October 7, at 11 am

Parliamentary Press Gallery (Ottawa) - Room 135B West Block

The Euthanasia Prevention Coalition (EPC) is hosting a press conference at the Parliamentary Press Gallery in Ottawa on October 7 at 11 am.


Dr Normand-Rivest
Speakers include: 

  • Dr Laurence Normand-Rivest, is a family physician in Montréal who cares for geriatric patients and provides in-home palliative care,
  • Dr Paul Saba is a family physician in Lachine Québec who has personal experience with caring for people with mental health related trauma,
  • Odile Marcotte, is a retired professor from the Université du Québec à Montréal and a former deputy director of the Centre de recherches mathématiques, and a EPC Board member.
  • Alex Schadenberg, Executive Director of the Euthanasia Prevention Coalition

Dr Paul Saba
Dr Normand-Rivest and Dr Saba will focus on their professional and clinical experience while Odile Marcotte and Alex Schadenberg will focus on the issues related to Bill C-218.

On June 17, 2026; the report of the Special Joint Committee on Medical Assistance in Dying (AMAD): Mental Disorder as the Sole Underlying Medical Condition: A Complex and Challenging Conversation Among Canadians - decided that the Government of Canada should amend the Criminal Code to indefinitely exclude persons whose sole underlying medical condition is a mental illness from eligibility for medical assistance in dying.

Odile Marcotte
The language of Bill C-218 enables the (AMAD) committee recommendation.

One of the reasons for the (AMAD) committee recommendation was that leading psychiatrists testified that it is impossible to determine if a mental illness or condition is irremediable. The law requires a person to have an irremediable condition in order to qualify for euthanasia.

For more information contact Alex Schadenberg at: 519-851-1434 or email: office@epcc.ca

To participate in-person or by zoom contact the Parliamentary Press Gallery at: pressres2@parl.gc.ca.

Seuls les membres de la tribune parlementaire peuvent participer à la période de questions et réponses, qui aura lieu sur place et via Zoom. Les médias qui ne sont pas membres de la tribune parlementaire peuvent communiquer avec pressres2@parl.gc.ca pour obtenir l'accès temporaire. 

The Euthanasia Prevention Coalition has almost 60,000 supporters from different political beliefs who unite in opposition to MAiD (euthanasia).

Tuesday, September 29, 2026

Issues with lethal injection execution are similar to euthanasia.

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

The NPR reported on September 28, 2026, in response to the botched lethal injection execution of Tony Carruthers on May 21, 2026 in Tennessee that a group of medical professionals sent a letter to Tennessee Governor Bill Lee stating that heathcare professionals should never assist with executions.

The letter by the medical professionals concerning the botched execution of Tony Carruthers stated:
The horrifyingly botched attempt to execute Tony Carruthers on May 21 confirmed that TDOC is not presently able to conduct an execution that complies with the law, its own protocol, or basic human decency.
Austin Sarat reported for The Daily Mail on May 26, 2026 that:
On 21 May, Tony Carruthers had an experience that few others have had. He was taken to the execution chamber, where the state of Tennessee began the process of putting him to death, but it failed to finish what it started.

Carruthers was not killed and he lived to tell about it. He became the ninth person to survive a failed execution in the last 80 years.

Botched executions are by now quite common in the United States. But on most of those occasions, the people whose executions go awry end up dead.
Catherine Sweeney reported for NPR that Dr Robert Quinn, one of the doctors who sent the letter to Governor Lee, stated that doctors should never participate in an execution.
He says that for one thing, the Hippocratic oath says, do no harm, and ethical codes, like the one put out by the American Medical Association, explicitly bar doctors from participating in the death penalty. The letter calls on Governor Bill Lee to place a moratorium on the death penalty and overhaul the state's execution method. They don't think executions should resemble medicine or involve doctors, nurses, pharmacists, or anyone else in healthcare. Dr. John Greer also signed the letter.
The death penalty and euthanasia (MAiD) both contravene the Hippocratic oath which requires the doctor to do no harm. 

Catherine Sweeney continued her NPR report:
Under Tennessee's protocol, other health workers, like nurses or paramedics, place IVs into the prisoner's arms. If they can't find a vein, a doctor must step in to insert a plastic tube, or central line, in a deeper vein. Regarding Carruthers' failed execution in May, the doctor said what he experienced was torturous. The IV team tried to access veins in his arms and failed. They tried his hands and his feet. Then the doctor tried a central line in Carruthers' chest and shoulder. His attorney, Maria DeLiberato, said blood was oozing from his puncture wounds.

...Finally, the governor's office called the prison. The governor was ordering them to stop. He gave Carruthers a one-year reprieve. The physician in Carruthers' execution,
The story about the euthanasia (MAiD) death of Brigitte Stegemann (83) who lived near Belleville Ontario presented a similar concern. The Daily Mail reported:
Once back inside the home, the nurse started the IV, Kranendonk alleges. According to Kranendonk, the doctor hadn't even arrived, and her grandmother was not asked if she gave consent for the procedure to begin.

The nurse struggled to insert the IV into Stegemann's right arm, and ended up piercing her repeatedly with the needle before attempting her left arm.

Kranendonk remembers in graphic detail the copious amount of blood, which made the whole procedure feel strangely unprofessional.

'She's asking us to hand her things, to flush out the needle. So we're now a part of this. She's asking us to grab things for her, and to hold things for her.

'This nurse is not wearing gloves. There's blood all over her hands, there's blood all over the place,' she says, horrified by the memory.
The letter to Tennessee Governor Lee also refered to the Post Traumatic stress that people have experienced after participating in a lethal injection death. The letter stated:
As medical professionals, we are also acutely aware of the risk of lasting trauma to all participants in the execution process. Many former correctional professionals have spoken out about the emotional toll of proximity to and participation in executions, including symptoms of post-traumatic stress, anxiety, depression, substance abuse, and suicidality. This risk is greatly exacerbated when executions go visibly awry, as in Mr. Carruthers’s case.
Whether or support or oppose capital punishment, the issues associated with lethal injection executions are the same issues that are associated with lethal injection euthanasia (MAiD).

The New York Times published a news article on June 11, 2026 by Rick Rojas and Abbie Van Sickle reporting that the Supreme Court appears to consider capital punishment by Nitrogen gas to be inhumane:
The Supreme Court’s decision was unsigned and included no reasoning, which is typical in such emergency rulings. Dissent came from three of the court’s conservative justices — Clarence Thomas, Samuel A. Alito Jr. and Neil M. Gorsuch.
The Supreme Court decision blocked the nitrogen gas execution of Jeffery Lee (49) who will remain on death row in Alabama.

On September 24, 2024, euthanasia activist, Dr Philip Nitschke, assisted the suicide of an American woman (64) who died by nitrogen gas asphyxiation in the Sarco pod.

If capital punishment by nitrogen gas is inhumane then assisting a suicide by nitrogen gas is also inhumane.

The difference between capital punishment and euthanasia (MAiD) is that capital punishment does not require a person to request to be killed whereas euthanasia, also known as medical homicide, usually requires a person to request to be killed.

The method of killing for lethal injection executions, is the same method of killing for euthanasia.

Monday, September 14, 2026

Ashley Dalton (Labour MP) speaks out against UK assisted suicide bill

Ashley Dalton UK (MP) L
This is the speech in the British parliament by Ashley Dalton (Labour MP) West Lancashire who is living with terminal cancer.

Dalton spoke out against the assisted suicide bill on Friday September 11, 2026. 

Dalton is not philosophically opposed to assisted suicide but she is concerned about it's effects and she was opposed to the bill which was defeated by a vote of 286 to 270. (Link to the speech) 


The last time this House considered this bill at Second Reading I was keeping a secret.

Whilst Honourable and Right Honourable members were debating the issue I was grappling with my own terminal diagnosis. I was told I have stage 4 incurable metastatic breast cancer.

I was overwhelmed with grief fear and anxiety. I was scared of what was to come and I was fearful of how it was to affect my family and my loved ones.

I was scared that I was going to get very poorly and thinking how will I cope, how will my family cope, I will I be cared for, how will I afford it, how badly will it hurt and how long will it last.

When you hear those words, depression anxiety, grief, shame and guilt come inbounds.

Suicide risk is highest immediately after diagnosis and it usually falls quickly within three to six months.

I would be lying if I said that when thinking about all that was to come I didn't consider that it might just be fairer and easier on everyone if I just got the dying done as soon as possible.

Having treatable depression however will not exclude anyone from an assisted death in this bill and depression is common among people with terminal illness but it is often treatable.

Clinicians are trained to prevent suicide in people suffering from depression, but where will the line be drawn. This bill makes no provision to support this difficult transition or to create safeguards around it.

A person can also be suicidal and have unmet mental health needs prior to developing a terminal illness and then ask the state to kill them without any assessment of their psychological health just their mental capacity. Because mental capacity and mental health are not the same thing.

The Royal College of Psychiatrists recommends a holistic multi disciplinary assessment of every applicant. The three person panel at the end of the assessment process in this bill is not what most NHS clinicians recognize as a multi-disciplinary team. It certainly does not allow the meaningful multi-disciplinary decision making. The assessment needs to happen at the beginning of the process, not the end and each team member should be independently assessing the patient, in person, this is not what is being included in this bill.

Now I don't know how long I will live. I will be on treatment for life, however how long or short that may be. I at the moment live between scans in 9 to 12 weeks blocks of time. The last scan may show that the disease is stable but the next scan may show that it is growing again. If the disease is stable the drug is working and we can carry on. Eventually the drug will stop working, the cancer will grow and we will have to try another drug and see if that works.

At some point we'll either run out of drugs to try or I will be too poorly to tolerate them. Then I die. It could be months, it could be years, no one really knows.
Prognosis is notoriously difficult to predict. Palliative care professionals and oncologists tell me that whilst they can more or less give me an indication of when I'll die when I'm a few days or weeks off, anything beyond that is a flip of a coin.

But what the palliative care professionals have told me is that palliative care can help me when I die.

But in the campaign around this bill it seems to me that it is being implied that a person with a terminal illness will have a dreadful painful death unless they have access to assisted dying and it is simply not true.

Palliative care in the UK is excellent. Far to many people do not have access to palliative care that they need. But the idea that it is not possible to alleviate pain and discomfort is false.

People, I, have been terrorized with tales of people vomiting up their own feces as though this is common place during death. It is vanishingly rare. Bowel obstructions are more common but they are treatable, I know, I have had one.

It's nothing short of irresponsible to scare monger people like me into believing that our deaths will be horrific when all the evidence suggests that with access to good palliative care deaths are, on the whole, gentle.

The answer is not to terrify people and their families. It's to sort out palliative care and social care first because of this takes place in a vacuum.

Until we can say that everyone who needs it has access to high quality palliative care then we are offering nobody a choice. A terrible death or an assisted death is not a choice it's a threat.

Whilst I speak today from the position of someone with a terminal illness, I am acutely aware that this is not about me. This debate is also not about an abstract concept or a position of principle. The question that will be put at the end of this debate will not be that this House has considered the question of assisted dying it won't even be that this House agrees with the principle of assisted dying. The question will be that this House agrees that this bill be read for a second time. This bill. Not the bill it might have been, not the bill members might have hoped it would be, not the bill it could be. This bill. And it incidentally it says absolutely nothing about the House of Lords. That is not the question that we are being asked.

And whatever Honourable and Right Honourable Members think about the principle of assisted dying surely our first and foremost responsibility is to write law that is safe and workable.

Not one of the professional bodies that will be tasked with delivery of the bill will attest that it is either safe or workable. The Royal College of Psychiatrists, the Association of Palliative Medicine, the Royal College of Physicians all say the bill is seriously inadequate. They aren't opposed to assisted dying in principle, but they cannot support this bill.

Instead of bringing a bill identical to the last so the Parliament Acts could be used and it can be forced, un-amended on the statute books, why didn't the proposers spend the summer working with the Royal Medical Colleges, professional bodies and organizations to build a bill that they could also support. If they had done that it would have been very difficult for those opposed to principle to argue against the bill, but they didn't. This is not about sides, this House is not a debating society, it is about making the law.

Whilst we may be campaigners out there, in here we are all legislators. It is our responsibility not to pick a side and dig in but to work together to build the best laws that we can and that is never truer than with a private members bill on a matter of conscience.

This bill does not protect the most vulnerable, it does not protect the poor, the old, people with disabilities or black and minority and ethnic people being disproportionately affected. It does not protect people who are mentally ill, it does not recognize that not everyone has the same level of agency, control or influence over their decision making and what the clinicians who are asked to deliver the bill are saying is that it isn't even workable. That there is every expectation that it wouldn't even work for the terminally ill people who want an assisted death either.

And there is no stopping it. Auto commencement in the bill means that if it is passed by the commons and pushed through by the Parliament Act and even it the government and NHS is not ready it has to happen on the strike of four years from it being passed. Even if there is no funding, even if palliative care is still broken, even if it is known to be dangerous flawed or unworkable, it is happening - ready or not.

This is not a last chance saloon. This debate has been going on for years, it is not a once in a generation opportunity, it could come back again at the next parliament.

My days could be numbered but that doesn't mean that I want this Chamber to rush through bad law just so I might have a chance to see it or use it. It's of huge importance.

If Honourable and Right Honourable members have any doubt that the exact bill before us today is not the best it could be. Is anything less than excellent well thought out and robustly drafted legislation that protects the vulnerable and recognizes the expertise of our world class clinicians, and a bill that I and other terminally ill people deserve, then I urge them to vote NO or vote to abstain.

The Euthanasia Prevention Coalition agrees with nearly everything that Dalton said, but we, of course, oppose killing people in general, as much as we recognize that the British bill was completely flawed. 

Friday, September 11, 2026

Great news: British parliament defeats assisted suicide bill.

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

I have great news.

The British Parliament defeated the Edwards assisted suicide bill today (September 11) by a vote of 286 to 270. This is a great reason to celebrate.

We especially congratulate our friends at the Care Not Killing Alliance who have worked for so long to defeat this bill and previous bills. 

EPC letter sent to members of the British parliament (Link).

Some background

The Edwards assisted suicide bill was introduced on June 17, 2026 and was nearly identical to the Leadbeater bill that passed in the British parliament on November 29, 2024 by a vote of 330 to 275 at second reading and 313 to 291 in the final vote.

The Leadbeater assisted suicide bill was fatally flawed and timed-out in the British House of Lords earlier this year.

What changed between November 29, 2024 and September 11, 2026?


The Leadbeater bill passed in the House of Commons but stalled in the House of Lords. During the House of Lords debate multiple flaws and concerns with the bill were uncovered. Even though the Leadbeater bill was flawed, Edwards introduced a nearly identical bill in order to invoke the Parliaments Act which states that if two nearly identical bills are passed in the House of Commons in two consecutive parliaments then the bill is not required to be approved by the House of Lords.

Edwards was hoping to prevent the bill from having to be debated in the House of Lords.

Keir Starmer - Andy Burnham
Another change was that Keir Starmer was the British Prime Minister during the Leadbeater assisted suicide bill debate. Starmer was a long-time promoter of assisted suicide.

Due to his drop in popularity, Starmer resigned as Prime Minister and Andy Burnham became the new Prime Minister.

Unlike Starmer, Burnham is not a strong supporter of assisted suicide. In late July Burnham, while speaking with reporters after a speech at a Jewish Care facility about social care reform commented on the upcoming assisted suicide debate. Burnham stated at (11:34):
"I take the view that the debate, and I don't say that there shouldn't be a debate at some point about those issues, personally I think that there is something that needs to happen first and that's the fixing of the funding of palliative care and social care. 
I think it is very challenging to introduce that wider debate in a context of people not receiving that care and having the peace of mind about that care.”
Burnham did not say that he opposed assisted suicide but he did say that improvements to end-of-life care should come first, before Britain considers assisted suicide.

Burnham later stated that members of the governing Labour party were not going to be pressured to vote for the assisted suicide bill.

Finally, stories about Canada's euthanasia law continue to circulate in Britain. The assisted suicide lobby has tried to "undo" the damage from Canada's euthanasia reality but the multitude of stories make it impossible to negate the truth, that legalizing assisted suicide, even a law that is "tighter" than the Canadian law, will result in expansion over time.

In March 2026, Scotland's parliament rejected the McArthur assisted suicide bill by a vote of 69 to 57 and today, the British parliament rejected the Edwards assisted suicide bill by a vote of 286 to 270.

The battle is not over in Britain, but the victories are worth celebrating.

Thursday, September 3, 2026

British government admits that disabled people may face ‘subtle pressure’ to choose assisted suicide, if bill passes

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

John Pring reported for the Disability New Service on September 3, 2026 that the British government admitted that disabled people may face 'subtle pressure' to choose assisted suicide if the assisted suicide bill becomes law. Pring reported that:
The impact assessment was published by the Department of Health and Social Care (DHSC) and the Ministry of Justice (MoJ) last Thursday (August 28).

The assessment’s publication came on the same day that prime minister Andy Burnham wrote to Labour MPs to say he would not vote on the bill on 11 September because he did not want to “unduly influence the debate as prime minister”.

He had already told the media that he believed the funding crisis in palliative and social care should be fixed before there is any debate about legalising assisted dying.

And he has now also told ministers that as the government will remain neutral on the bill, they should “avoid being part of the public debate, and should not express views” about the implications of the bill for their own departments.
Pring reported that the government published three assessments of the assisted suicide bill on August 28.
On Thursday (28 August), DHSC and MoJ published three key documents that assess the “potential impacts” of the bill.

Their equality impact assessment of the bill accepts that disabled people “may be more susceptible to feeling as though they are a burden on those around them”, a key concern raised by campaigners opposed to legalisation.

The impact assessment says that this pressure “is not necessarily felt or applied by other people” but that disabled people “may feel subtle pressure due to attitudinal barriers or a lack of alternative appropriate services and support”, such as with the lack of access to palliative care.

It says these feelings of being a burden could also be caused by “structural pressures such as neglect, poverty and difficult living conditions”, while disabled people are twice as likely as non-disabled people to be victims of domestic abuse such as coercive behaviour.

And the equality impact assessment warns that factors such as high rates of poverty, poorer access to healthcare, lower quality care, and disproportionate levels of domestic abuse of black and Asian women could cause disproportionate numbers of minority ethnic people to choose an assisted death “to avoid financial hardship or escape abuse”.

It also highlights how older people, who are likely to be the main recipients of assisted dying, are “often dependent on those who care for them”, which puts them at increased risk of abuse and pressure to choose an assisted death.

And the assessment reports findings by the UN in 2021 that older people “may feel subtly pressured to end their lives prematurely”.
On November 29, 2024; the UK House of Commons voted 330 to 275 at second reading to support Kim Leadbeater's assisted suicide bill, a bill that was fatally flawed and died in the British House of Lords.

On June 17, 2026 Labour MP Lauren Edwards introduced a similar version to the Leadbeater bill that is scheduled to be voted-on at second reading on September 11, 2026.

The Euthanasia Prevention Coalition is convinced that Edwards introduced a nearly identical assisted suicide bill as the Leadbeater bill in order to invoke The Parliament Acts, which allows the House of Commons to forgo approval from the House of Lords when passing two nearly identical bills within consecutive parliamentary sessions.

Wednesday, September 2, 2026

Fix how we care for the most vulnerable. No to assisted suicide.

The following article by Zubir Ahmad was published by the Guardian on August 25, 2026.

Usually we comment on an article, but Dr Zubir Ahmad it was better to simply republish this article. The British parliament will once again vote-on an assisted suicide bill on September 11, 2026. The new bill is nearly identical to the previous bill.


Dr Zubir Ahmad
By Dr Zubir Ahmad 

As a doctor, I have spent much of my professional life caring for people at some of the most vulnerable moments they will ever face. I have seen the anxiety that surrounds the prospect of dying, and the desperate wish of patients and families to avoid unnecessary suffering.

Naturally, we all want people facing the end of life to be treated with kindness and respect. But when considering the debate on assisted dying, true compassion demands that we ask a more fundamental question. What kind of society are we building if, before we’ve fixed the systems designed to care for people, we introduce a system designed to help them die? As a former health minister who has seen the system from the inside, I am able to say it is not ready or equipped to answer this question.

Andy Burnham has been right to raise this as a priority issue at the start of his tenure as prime minister. Speaking at a care home recently, he explained that assisted dying should not be introduced while Britain’s palliative care and social care systems remain under such strain. A choice between death without adequate care and a death prematurely self-induced is not a real choice.

Indeed, as parliament prepares for yet another vote on assisted dying in England and Wales on 11 September, I fear that the offering has been somewhat mis-sold to the public. A state-controlled medicalised dying process is still a process – one where there remain risks of complication and suffering. The reality of assisted dying is more complex than the promise of a perfectly controlled death.

Many people imagine a system where a person facing a terminal illness can choose the exact moment and manner of their death, free from distress. But the legislation does not and cannot provide that certainty. A patient who self-administers medication to begin the dying process may still experience complications. The process may take time; it may require medical intervention. It may not happen where or when the person imagined. The promise of absolute control can therefore become something different in practice: an appearance of choice that does not always deliver the agency people expect.

I am far from the only medical professional to be worried about the prospect of assisted dying being available on the NHS. Among those raising concerns about the bill’s dozens of flaws have been the Royal College of Physicians, the Royal College of Psychiatrists, the Complex Life and Death Decisions (CLADD) group from King’s College London, the Royal College of Pathologists, the British Geriatrics Society and numerous other medical bodies and care authorities. The same concern comes up again and again: is it really a “free choice” when palliative care and social support fall short?

A person’s wish to die does not happen in isolation from their circumstances. It can be shaped by whether they feel supported, whether they fear becoming a burden, whether their family is coping and whether they have access to the care they need. That is why the state of our care systems cannot be treated as a separate issue from assisted dying. Timely access to palliative and social care remains too often determined by where someone lives rather than what they need. For some families, excellent end-of-life support is available; for others, particularly in rural areas as well as constituencies experiencing high inequality, the experience is one of waiting, uncertainty and having to fight for services that should be guaranteed.

A Labour government founded the NHS on a principle that remains as important today as it was at its creation: that healthcare should be there when people need it most, regardless of their circumstances. A postcode lottery in care cannot be ignored while debating a new legal pathway for people at the end of their life.

In Scotland, this concern has been expressed clearly, and was an important reason why, in March, 85% of Labour MSPs voted against the legalisation of assisted dying in Holyrood. The bill introduced in Westminster by my colleague Kim Leadbeater, the Labour MP for Spen Valley, in October 2024 did not fare much better: too many concerns about patient welfare meant the House of Lords would not rubber-stamp the flawed text. And yet, on 11 September, MPs will be faced with yet another vote on assisted dying before the care systems are improved to a level which even makes that debate appropriate. Andy Burnham has his priorities right: this is the wrong debate at the wrong time. This is why I, and many others, will be voting against this bill, in pursuit of comfort, dignity and appropriate care for people who are vulnerable and dying.

Zubir Ahmed MP is an NHS vascular and transplant surgeon, and served as the parliamentary under-secretary of state at the Department of Health and Social Care from 6 September 2025 to 12 May 2026.

Thursday, August 27, 2026

Nitschke will bring suicide pod to Britain if assisted suicide is legalized.

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

Philip Nitschke, also known as Dr Death, who invented a suicide pod, stated in an interview, last year, that the suicide pod will be ready for use in Britain if assisted suicide is legalized.

Sanchez Manning reported for the Times on June 20, 2025 that:

Nitschke, who invented the pod, which uses gas to assist death, said: “As soon as we know that the final legislation is in place we’ll start enthusiastically pursuing the option of using the device in the UK.

“We’ll be looking to find UK-registered doctors to assist and of course someone who wants to use it and satisfies all of the requirements under the law.”
In September 2024, long-time euthanasia activist, Philip Nitschke, carried out the first assisted suicide Sarco suicide pod death in Switzerland.

The suicide pod is promoted as an easy and pain free death. The pod is designed in a sleek manner to make it seem like a fashionable way to die. The pod causes death by releasing Nitrogen gas resulting in death within several minutes.

The UK House of Commons will once again debate the Kim Leadbeater assisted suicide bill which passed, by a vote of 330 to 275 on November 29, 2024 at second reading, in the UK House of Commons but died on the order paper in the House of Lords earlier this year.

The House of Lords debated multiple amendments to the flawed Leadbeater bill. The debate in the House of Lords (timed-out) before they voted on the bill.

Lauren Edwards, (Labour MP) for Rochester and Strood, had reintroduced the Leadbeater bill, that is scheduled to have it's first vote on September 11, 2026. The Edwards bill is nearly identical to the Leadbeater bill and therefore may not be required to be debated in the House of Lords, if it passes at final reading in the UK House of Commons based on the rule that if a nearly identical bill passes twice in consecutive parliaments, then it is not required to be debated in the House of Lords.

More recently Nitschke has been promoting the KK suicide "collar" which, when activated, will essentially strangle the person to death.

Nitschke has become a notorious and wealthy promoter of suicide through the sale of his books and devices. He has become famous with the creation of his "suicide pod" that is designed to gain media attention.

Nitshcke is known for his support for suicide on demand. He once told a reporter that even troubled teens should have access to the "peaceful pill".

Nitshke is not an "outsider" in the euthanasia movement. He has been a leader and world-wide euthanasia activist since the mid 1990's when he became the first doctor to legally kill patients in Australia's northern territory that had legalized euthanasia in 1995 but the law was overturned in 1997.

The sad news is that Australia's Northern Territory once again legalized euthanasia on August 27, 2026. 

Thursday, August 13, 2026

Lawsuit filed to prevent assisted suicide in Illinois.

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

We reported on December 12, 2025 that Illinois Governor JB Pritzker signed assisted suicide bill SB 9 into law. The Illinois assisted suicide law is scheduled to go into effect on September 12, 2026.

A group of Illinois physicians, a Catholic bishop and a faith-based nursing home filed a federal lawsuit seeking to block Illinois’ assisted suicide law before it goes into effect.

John Clark reported for mystateline.com on August 12 that:
The lawsuit, filed Tuesday in the U.S. District Court for the Northern District of Illinois, argues that the state’s End-of-Life Options Act violates constitutional protections for free speech, religious freedom and due process by requiring physicians and health care organizations that oppose assisted suicide to participate in the process against their beliefs.

Clark reports that the Illinois lawsuit is based on preventing assisted suicide and protecting freedom of speech, conscience rights and religious freedoms:

However, the new lawsuit argues that objecting physicians and institutions are still required to discuss what the law describes as end-of-life options, provide information or referrals to willing providers, and comply with other requirements that conflict with their religious beliefs and medical ethics.

The plaintiffs contend those provisions force them to endorse or facilitate actions they believe are morally wrong.

According to the complaint, the physicians object to informing patients about what the law characterizes as the benefits of medical aid in dying, referring patients to providers willing to participate, documenting certain requests in medical records, and complying with provisions governing death certificates.

Clark states that the lawsuit is seeking an injunction against the assisted suicide law. 

The suit asks the court to issue a temporary restraining order, preliminary injunction and permanent injunction blocking enforcement of those provisions before the law’s Sept. 12 effective date. Plaintiffs also seek declarations that portions of the law violate the U.S. Constitution, the Americans with Disabilities Act and certain federal health care statutes.

A similar lawsuit was filed in New York to prevent the implementation of their assisted suicide law. On July 31, 2026; The Beckett Fund reported that a temporary order was obtained preventing the state of New York from forcing Catholic Sisters and Catholic healthcare from participating in the assisted suicide law while the federal lawsuit by Catholic healthcare proceeds in the court.

The lawsuit instituted by the Beckett Fund has temporarily protected Catholic Healthcare from being forced to participate in assisted suicide but it has not achieved an injunction to prevent the New York assisted suicide from going into effect. 

On June 11, we reported that The Institute for Patients' Rights joined two federal lawsuits, one in New York and one in Illinois, with a coalition of national and state-based disability and patient advocacy organizations. For both states, Not Dead Yet, United Spinal Association, and the National Council on Independent Living, are organizational plaintiffs.

Euthanasia in France—Contrary to the Constitution, Hope, and Dignity

Open Letter to the Members of the Constitutional Council: Medical Aid in Dying in France—Contrary to the Constitution, Hope, and Dignity

Dr Paul Saba
By Dr Paul Saba, a family physician in Lachine Quebec.

You only need to walk through the halls of a hospital long enough to discover the reality that lies behind the numbers. Patients aren’t just medical records; they’re people. The difference between hope and despair often comes down to a door that opens… or remains closed. The new laws on assisted suicide claim to be about choice, but anyone who has worked in the medical field knows how quickly that “choice” crumbles under pressure. There’s the cancer patient living in a cramped, noisy apartment; the woman with a disability who can’t afford to go grocery shopping; the elderly man living alone who fears for his future. They’re told they have the right to die with dignity, but what they really need is the right to live with dignity.

Canada’s experience should give us pause for thought. Since 2016, when the law was first enacted, 100,000 Canadians have died by medical assistance in dying, many of whom still had years, even decades, left to live. What was initially presented as an option reserved for terminally ill patients has expanded to include people with chronic illnesses and mental health conditions. Quebec alone accounts for 8% of the total deaths by assisted dying, the highest rate in Canada and worldwide. These numbers are rising every year.

Initially, the system was based on strict criteria, but the boundaries have quietly shifted. We are hearing more and more stories of people requesting assisted dying because they are unable to access home care, accessible housing, or adequate food. “Dignity” is becoming a code word for cost-cutting, while the most vulnerable find themselves facing a maze with no way out. Consent is not a box to check. It is a conversation, a process, and, above all, a reflection of the options available to the individual.

When a person is sick, frightened, and overwhelmed by bills, to what extent is their freedom of choice truly real? Loneliness and poverty influence decisions just as much as physical distress or a diagnosis. Advocates for this cause believe that safeguards will hold firm, but in practice, the boundaries are shifting. The line between compassion and abandonment is blurring, especially when budgets are tight and beds are scarce. I have seen families exhausted by the burden of care, patients who would rather disappear than ask for help, and medical staff powerless in the face of bureaucracy.

France, just like Canada, lacks adequate health care, particularly when it comes to general practitioners, emergency room doctors, and timely access to specialists. Legalizing assisted suicide without fixing our failing health care systems is tantamount to telling people that some lives are too complicated to be supported. It is easier to pass a law than to put a safety net in place. True dignity comes from community, commitment, and the refusal to abandon anyone. Until every patient has a comfortable bed, quality care, and a sympathetic ear, we will not have the right to offer a way out.

Beyond these practical and moral concerns, the French bill also contradicts the country’s Constitution.

First, unlike in France, where the protection of health enjoys constitutional recognition (Preamble to the Constitution of October 27, 1946, para. 11, incorporated into the constitutional framework; see, in particular, the case law of the Constitutional Council), the Canadian Constitution contains no provision expressly guaranteeing such a right. The constitutional mandate of the French state is to protect life and health by guaranteeing access to care, treatment, and palliative care, rather than by establishing a medical aid in dying program.

Furthermore, the law on medical assistance in dying disproportionately affects vulnerable groups, particularly people with disabilities, chronic illnesses, or associated mental health conditions who, in the absence of adequate care and social support, may feel pressured to end their lives prematurely. This constitutes a direct violation of the constitutional right not only to health and life but also to equality, as it creates a situation where certain citizens are effectively encouraged to die because their needs are not being met.

Similarly, the principle of liberty requires that consent be free and informed. However, when a person is experiencing physical or associated psychological distress, is isolated, and lacks support, their ability to make a clear and not coerced decision is compromised. The law’s failure to guarantee truly voluntary consent risks undermining this fundamental constitutional liberty.

Let me tell you a story. Eight years ago, John (a pseudonym), a highly knowledgeable engineer, came to see me for a cough. A chest X-ray suggested lung cancer. He could have given up at that point, since Canadian law allows patients to refuse tests and seek assisted dying prematurely. But I convinced him to undergo further testing. It turned out to be Hodgkin’s lymphoma, It is entirely treatable. Today, John is alive and in good health.

Unfortunately, a recent study revealed that 13% of patients who died by assisted suicide after a diagnosis of lung cancer had never undergone a biopsy to confirm the diagnosis and were less likely to consult oncologists or receive treatment.

Another patient, Rachel (also a pseudonym), in her 50s, was diagnosed with breast cancer. After surgery, tumor cells remained and grew rapidly. At first, frightened and desperate, she refused chemotherapy and immunotherapy, even going so far as to stop eating. Eventually, she agreed to treatment and made a full recovery. Rachel said that cancer can drive a person crazy and cloud their judgment. It was hope that saved her. 

These are not isolated cases. As a physician responsible for reviewing cases of assisted dying, I find that most involve people suffering from medical conditions or disabilities exacerbated by social isolation, feelings of being a burden, loss of autonomy, and psychological distress. Physical pain, which could be relieved, is often the least common reason.

A recent study estimated that making assisted dying available to vulnerable groups in Canada—including, but not limited to, the homeless, people with substance use disorders, retirees, the elderly, and Indigenous communities—could save 1,273 billion CAD (791 billion EUR) by 2047, resulting in 2.6 million deaths. This scenario could easily apply to France if it were to follow the same path.

This raises a frightening question: Are we broadening eligibility criteria to eliminate citizens for financial gain rather than to care for and support them? This approach devalues human life and fosters a dangerous mindset, according to which the easy solution to complex health and social problems is to eliminate vulnerable individuals rather than invest in care. It creates a conflict of interest in which governments profit, directly or indirectly, from the deaths of their citizens. It also raises profound ethical questions for healthcare professionals.

France has the opportunity to prevent this. Do not be fooled by rhetoric about autonomy and dignity when basic needs are not being met. Assisted dying destroys hope. It pushes people to give up before their time. Hope is the greatest strength of quality care—the conviction that every step forward counts. Assisted dying prematurely puts an end to that hope.

I urge you to protect the most vulnerable, to invest in care, and to reject laws that offer shortcuts instead of safety nets and options for extended care. Until every patient has access to the care, support, and dignity they deserve, no law authorizing assisted dying can be considered, much less regarded as an act of compassion.

Respectfully, 
Dr. Paul Saba 
Maître Natalia Manole 

Dr. Paul Saba is a Canadian physician who has practiced medicine around the world. He currently practices family medicine in Montreal. He is a co-founder of the Physicians' Alliance against Euthanasia (https://collectifmedecins.org/en/about/) and author of the book *Made to Live* (madetolive.com) +1 514-886-3447 

Saturday, August 1, 2026

UK Prime Minister seeks to delay assisted suicide debate

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

Prime Minister Andy Burnham
The new UK Prime Minister, Andy Burnham, while speaking with reporters after a speech at a Jewish Care facility about social care reform commented on the upcoming assisted suicide debate. Burnham stated at (11:34):
"I take the view that the debate, and I don't say that there shouldn't be a debate at some point about those issues, personally I think that there is something that needs to happen first and that's the fixing of the funding of palliative care and social care. 
I think it is very challenging to introduce that wider debate in a context of people not receiving that care and having the peace of mind about that care.”
Burnham did not say that he opposes assisted suicide but he did say that improvements to end-of-life care should be dealt with first, before the UK considers assisted suicide.

These comments are important because on June 17, 2026 Labour MP Lauren Edwards introduced a similar version of the Terminally Ill Adults (End of Life) Bill that recently died in the British House of Lords. MPs are scheduled to vote on the Edwards assisted suicide bill at second reading on September 11, 2026.

On November 29, 2024; the UK House of Commons voted 330 to 275 at second reading to support Kim Leadbeater's assisted suicide bill, which was nearly identical to Edwards bill

The Euthanasia Prevention Coalition is convinced that Edwards introduced a nearly identical assisted suicide bill as the Leadbeater bill in order to invoke The Parliament Acts, which allows the House of Commons to forgo approval from the House of Lords when passing two nearly identical bills within consecutive parliamentary sessions.

The Parliament Acts has only been used seven times since 1911 for Government legislation, and it has never been used for a Private Members’ Bill. Edwards assisted suicide is a private members bill.

Prime Minister Burnham's comments along with the fact that he has given members of his Labour party the right to vote with their conscience means that the Edwards assisted suicide bill will more likely be defeated on September 11.

Thursday, July 23, 2026

The British assisted suicide bill is back - And so is Not Dead Yet.

The following message was sent out by Not Dead Yet UK on July 23, 2026.

By now you'll know that the assisted dying bill is back.

On 17 June, Labour MP Lauren Edwards introduced a new version of the Terminally Ill Adults (End of Life) Bill. MPs will vote on whether it should proceed at its second reading on 11 September 2026. That's less than two months away.

So what's new?

Honestly? Not much.

This is the same bill Kim Leadbeater brought forward in 2024 — the one that spent months being picked apart in the House of Lords, generating more than 1,300 amendments before running out of time in April. The bill fell not because it was defeated, but because Parliament was prorogued. Now it's back, with two minor Lords amendments incorporated.

The first is a technical Wales amendment. Because delivering health services is devolved to the Welsh Government, the bill now requires the Senedd to give its approval before Welsh Ministers can set up the regulations for assisted dying in Wales. It's a constitutional housekeeping change. It doesn't alter what the bill actually does.

The second concerns people with eating disorders. This one is more serious. During the Lords debates earlier this year, peers raised concerns that someone with anorexia could potentially stop eating — deliberately — in order to reach the six-month terminal threshold and qualify for an assisted death. A minor amendment was added in the Lords to address this. But experts who work with people with eating disorders say it doesn't go far enough. The loophole, they argue, remains. We agree.

Everything else about the bill — its safeguards, its eligibility criteria, its scope — is unchanged. The concerns we have always raised remain. Disabled people face cuts to their independence, support, and care. Palliative care is under-resourced. In that environment, telling people they have the option to end their lives early is not compassion. It is a profound risk to people who already feel like a burden.

Even the new Prime Minister, Andy Burnham, has acknowledged this. He has said he supports the principle of assisted dying — but only if hospices are "properly funded and sorted out" first. "You can't have this law change with an underfunded hospice movement," he said. We agree. And that underfunding hasn't been fixed.

What we're doing about it.

We are meeting very shortly to put the final touches to our campaign strategy for September. Our main goals are:
  • Persuading MPs to vote against the bill at second reading on 11 September.
  • Organising a demonstration outside the Houses of Parliament on the same day.
We will be in touch with full details as soon as they're confirmed — including how you can write to your MP, join us in person, or support the campaign in other ways.

We know many of you have been with us since the beginning of this fight. Your support matters enormously. We are not done yet.

Friday, July 17, 2026

UK assisted suicide bill will go to a vote on September 11, 2026

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

The UK Leadbeater assisted suicide bill that failed to pass earlier this year in the House of Lords has been revived by Lauren Edwards MP with nearly identical language as the failed Leadbeater bill.

On November 29, 2024; Members of the UK House of Commons voted 330 to 275 at second reading to support Kim Leadbeater's assisted suicide bill.

The Euthanasia Prevention Coalition urges the UK to Kill the bill not the patients.

The Care Not Killing Alliance stated in their July 17 report that:

Yesterday, Lauren Edwards MP published her Private Member’s Bill. We say “her” bill, but it is essentially the same as the one which foundered in the Lords earlier this year: they could have taken this opportunity to reflect and respond to the many concerns of experts and professional groups, but the clear priority is to leave open the door to use of the Parliament Acts, and so you can be sure that there will be strenuous efforts to prevent MPs from seeking amendments to the Bill.

The House of Lords debate exposed serious flaws with the Leadbeater assisted suicide bill and yet Edwards insists on pushing the same flawed bill because, if passed by the House of Commons, it would not be required to be debated by the House of Lords, where strong opposition to assisted suicide exists.

The Parliament Acts have only been used seven times since 1911 for Government legislation, and it has never been used for a Private Members’ Bill. Edwards assisted suicide is a private members bill.

The Euthanasia Prevention Coalition is convinced that Edwards, who is a Labour MP for Rochester and Stroud, has introduced a nearly identical assisted suicide bill as the Leadbeater bill in order to invoke The Parliament Acts, which allows the House of Commons to forgo approval from the House of Lords when passing two essentially identical bills within consecutive parliamentary sessions.

A similar parliamentary tactic was used in France where the National Assembly passed identical euthanasia bills on June 30 and July 15 that enabled them to ignore the opposition to the euthanasia bill in the Senate, even though France's Senate is elected.

California also legalized assisted suicide in 2015 with a similar tactic.

Concerning California, on August 18, 2015 we wrote:

The assisted suicide lobby has renewed their push to legalize assisted suicide in California after their previous assisted suicide bill, SB 128, was stopped in the Health Committee.

The assisted suicide lobby is taking advantage of the special legislative session called by Governor Jerry Brown to address shortfalls in healthcare funding. The new assisted suicide bill AB 15 is nearly identical to SB 128, but AB 15 will not be heard by the Health Committee.
In other words, SB 128 was stopped in California's Health Committee, then Governor Brown opened a "special session" to examine shortfalls in healthcare funding that included Bill AB 15, an identical assisted suicide bill to SB 128, which passed in the special session and became law.
 
Edwards appears to be using the same playbook that was used recently in France and in 2015 in California.
 
Kill the bill, not the patients. 

Thursday, July 9, 2026

Jersey assisted suicide bill receives Royal Assent

The following is a media release from the Care Not Killing Alliance on July 9, 2026.

Care Not Killing deeply disappointed as Jersey’s assisted dying law receives Royal Assent despite ECHR breaches

Campaign group Care Not Killing has expressed deep disappointment following the decision to grant Royal Assent to Jersey’s Assisted Dying (Jersey) Law 2026, making Jersey the first part of the British Isles to legalise assisted dying.

The group believes the legislation breaches the UK’s obligations under the European Convention on Human Rights — including Article 2 (right to life), Article 9 (freedom of conscience), Article 10 (freedom of expression), Article 11 (freedom of association), and Article 14 (freedom from discrimination) — and that this is precisely why Royal Assent had been held up for so long.

In a legal letter sent to the Attorney General of Jersey and the Ministry of Justice on 21 May 2026, Care Not Killing’s solicitors, Conrathe Gardner LLP, set out a series of concerns about the Law’s compliance with the ECHR. The letter warned that the legislation places vulnerable individuals at “severe risk of loss of life in a way that is discriminatory and impermissible under the ECHR.”

It highlighted that the law fails to adequately test for coercion, duress or undue influence — particularly in the case of disabled people — by relying on “an assessing doctor simply asking the individual if anyone has coerced them.”

The letter also noted that individuals with conditions such as bipolar disorder, depression, and autism face significantly higher rates of suicidal ideation, and that the Law makes no provision to protect them.

Care Not Killing pointed to the well-documented expansion of euthanasia regimes in other jurisdictions — noting that in Canada, one in twenty deaths is now by assisted suicide, and in the Netherlands, 5.4 per cent of all registered deaths are by assisted suicide with uptake increasing by 8 per cent every year.

The group also highlighted that even before the Law was passed, a proposition was tabled to extend it to incurable (non-terminal) conditions, and that Health Minister Tom Binet has stated this amendment will be proposed again in future. The Law also introduces so-called “safe access” zones that could criminalise prayer and sermons in places of worship near where assisted dying takes place, interfering with rights under Articles 9, 10 and 11 of the ECHR.

Dr Gordon Macdonald
Dr Gordon Macdonald commented: 
“This legislation will fundamentally alter health and palliative care on Jersey and put the lives of vulnerable people at risk, exactly as we have seen in those places that have introduced assisted suicide or euthanasia. It fails on a number of fronts, including: lack of legal protections for doctors and nurses who do not want to be involved, protections for the elderly and disabled people at risk of being coerced, will see money taken out of palliative care and has been sold to the public as a way to end suffering when we know from places like Oregon, those who take the death row drugs may suffer long and agonising death from a pulmonary oedema - where their lungs slowly fill up with bodily fluid and the drown in their own secretions.

“Importantly, as our lawyers have pointed out, this law does not comply with the European Convention on Human Rights and is not compatible with the UK’s obligations under the Convention on the Rights of Persons with Disabilities. We will be consulting our lawyers to determine our next steps and how and when this dangerous law can be challenged.”
For media inquiries, please call Alistair Thompson or Team Britannia PR on 07970 162225.

Editors Notes

Care Not Killing was founded as a UK-based alliance of human rights and disability rights organisations, health care and palliative care groups, faith-based organisations groups, and is supported by thousands of concerned individuals.

We have three key aims:
  • to promote more and better palliative care;
  • to ensure that existing laws against euthanasia and assisted suicide are not weakened or repealed;
  • to inform public opinion further against any weakening of the law. 

*As this story is dealing with suicide, please could we ask that you include details about organisations that offer help and support to vulnerable people who might be feeling suicidal such as the Samaritans, CALM or similar - Thank you.*