PJ Psych: Assisted suicide is being fast-tracked: what about those of us living with despair?

The British Journal of Psychiatry


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Assisted suicide is being fast-tracked: what about those of us living with despair?

Published online by Cambridge University Press:  09 February 2026

James Downs[Opens in a new window]

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Keywords

Suicidestigma and discriminationassisted dyingpsychiatry and lawhuman rights


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TypeLetterInformation

The British Journal of Psychiatry First View , pp. 1 – 2

DOI: https://doi.org/10.1192/bjp.2026.10535[Opens in a new window]

Copyright

© The Author(s), 2026. Published by Cambridge University Press on behalf of Royal College of Psychiatrists


In writing this letter, I do not intend to debate assisted suicide itself. Rather, as someone who lives with chronic suicidality due to mental illness, I have found the recent discourse around ending one’s life complicated and painful. Although there are fundamental differences between living with chronic suicidality and the process of dying, Reference Friesen1 the policies being considered by legislators bring into focus the persisting disparities in how society understands and responds to mental illness as compared with physical illness.

The UK Parliament’s proposed legislation for assisted suicide, as a legal and clinical service, is framed as a compassionate response to those experiencing refractory end-of-life suffering. Reference Burki2

As the UK moves towards implementing assisted suicide for people with terminal illnesses, the public debate has been shaped by advocates who emphasise dignity, personal autonomy and compassion. Reference Harwood3 These are values we all want to see upheld in healthcare: compassion is a foundational ethical principle across health professions, embedded in medical guidelines internationally. Reference Behan and Kelly4

What does it mean when the desire to die is met with compassion and understanding in one context, but feared, dismissed or punished in another?

Living with chronic suicidality

I have lived with suicidal thoughts stemming from complex mental illness for the most part of two decades. There are times when I want to die more than anything else. There are also times when I desperately want to live but can’t feel any hope. In between, there are long periods where I survive more than I live and have very few days without some kind of ambivalence between wanting (and not wanting) to live (or to die).

Awareness campaigns encourage us to ‘reach out’, Reference Henderson, Robinson, Evans-Lacko and Thornicroft5 but I’ve only ever been able to access clinical care after a crisis. Even then, I have often felt blamed for my symptoms by professionals who have labelled them as ‘attention seeking’ or used the abstract word ‘behavioural’ to explain them. Conversations about suicidality, on the few occasions when they have taken place, have rarely been compassionate.

The right kind of suicidal

The debate around assisted suicide both highlights and reinforces a persisting divide in how society regards physical suffering versus mental suffering. Reference Behan and Kelly4 The person whose body is failing owing to terminal illness has their pain acknowledged as legitimate. They are not seen as irrational; their death is part of the natural order, and their decision is met with empathy. New services for them have been modelled at pace in Parliament, with the promise of all the funding they need.

This lies in stark contrast to the lack of progress in providing understanding and support for those who feel suicidal as a result of mental illness. Many of us wait years for any meaningful response at all. The services we need are under-resourced, or do not exist. The message this sends is clear: there is a ‘right’ kind of suicidal, and ours is not it.

This hierarchy has significant clinical consequences. When mental illness is seen as a form of suffering that is less worthy of attention and support, this reinforces stigma and hopelessness, creating a damaging cycle in which people are discouraged from seeking help or seeing their struggles as valid.

Compassion as a safeguard

Assisted suicide is framed as a compassionate act, preventing the distress of a painful death. But compassion is not always about alleviating suffering, nor it merely a sentiment. Compassion is something that is enacted – through empathy, presence and kindness. Reference Gilbert6 These practices depend on the structures of healthcare, including sufficient training and resources that equip clinicians with the skills and space to offer compassion ate responses sustainably. Reference Harwood3,Reference Baguley, Pavlova and Consedine7

In my own experience, I am grateful for the times when clinicians enacted compassion in ways that were not necessarily ‘soft’ – for being fiercely protective of my life when I have wanted to discard it. I am here today because of professionals who have held a firm line with me, even when I have pushed them away, and have understood that the kind thing to do doesn’t always feel kind for the patient, or for themselves.

If we’re going to talk about assisted dying with the language of compassion, then we need to talk about compassionate responses to mental illness with the same depth and nuance. Reference Malhi8 For someone like me, who isn’t dying but often wants to, I need the law to protect me: from under-resourced systems, from clinicians afraid to talk about suicide and from myself on the days when I am convinced that dying is the answer. That, to me, is compassion.

The same nuance is needed when considering patients’ rights to make decisions. Achieving parity of esteem between mental and physical illness is not about offering the same outcome. Although patients have rights, that doesn’t mean that our views are always right, especially when we are in the grip of suicidality. This is when our right to life must take priority, even if it is not our own priority at the time.

Making space for suicidality

Too often, clinicians have either treated my suicidality as a pathology to be controlled and a risk to be managed, or ignored, trivialised and dismissed it as something I’m not really that serious about. In both cases, the reality of my suffering has been sidestepped, either by being erased or denied. Between these two forms of avoidance has been my unmet need for attention, presence and listening. What I have needed most has been someone to sit with me in my suffering and to listen without trying to change, minimise or deny my experience.

Being alongside those who are suicidal is not about agreeing with their thoughts or actions; it is about embedding listening and presence as central components of compassionate care, especially in the context of systems where these practices can easily be overshadowed by excess pressures and efficiency demands. Reference Gilbert6 Public discourse and clinical practice alike need to make recognise that the suffering of mental illness deserves to be met with just as much resource, respect and compassion as terminal illness.

If dying well matters, so should living

I want people who are dying to have as much support as possible to die well. But I also want people who are suicidal to have the chance to live well. Part of this is being able to speak about wanting to die without being met with fear or avoidance. It also requires clinical environments in which staff have the time, training and support to respond with empathy and presence, so that compassion becomes a lived reality rather than an aspiration.

If our politicians can fast-track services to assist those with terminal illnesses to die, they must also act to improve the healthcare that is offered to those who are choosing, every day, to stay alive.

Funding

This letter received no specific grant from any funding agency, commercial or not-for-profit sectors.

Declaration of interest

None.


References

1

Friesen, P. Medically assisted dying and suicide: how are they different, and how are they similar? Hastings Cent Rep 2020; 50: 32–43.10.1002/hast.1083CrossRefGoogle ScholarPubMed

2

Burki, T. UK House of Commons passes assisted dying bill. Lancet Oncol 2025; 26: 997.10.1016/S1470-2045(25)00405-XCrossRefGoogle Scholar

3

Harwood, RH. We should not fear assisted dying. Age Ageing 2025; 54: afaf029.10.1093/ageing/afaf029CrossRefGoogle Scholar

4

Behan, C, Kelly, B Handbook of Compassion in Healthcare: A Practical Approach. Cambridge University Press, 2025.10.1017/9781009390217CrossRefGoogle Scholar

5

Henderson, C, Robinson, E, Evans-Lacko, S, Thornicroft, G. Relationships between anti-stigma programme awareness, disclosure comfort and intended help-seeking regarding a mental health problem. Br J Psychiatry 2017; 211: 316–22.10.1192/bjp.bp.116.195867CrossRefGoogle ScholarPubMed

6

Gilbert, P. Compassion: from its evolution to a psychotherapy. Front Psychol 2020; 11: 586161.10.3389/fpsyg.2020.586161CrossRefGoogle ScholarPubMed

7

Baguley, SI, Pavlova, A, Consedine, NS. More than a feeling? What does compassion in healthcare ‘look like’ to patients? Health Expect 2022; 25: 1691–702.10.1111/hex.13512CrossRefGoogle ScholarPubMed

8

Malhi, GS. Assisted dying for mental illness: a contemporary concern that requires careful and compassionate consideration. Br J Psychiatry 2024; 225: 259–61.10.1192/bjp.2024.116CrossRefGoogle ScholarPubMed

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About michelleclarke2015

Life event that changes all: Horse riding accident in Zimbabwe in 1993, a fractured skull et al including bipolar anxiety, chronic fatigue …. co-morbidities (Nietzche 'He who has the reason why can deal with any how' details my health history from 1993 to date). 17th 2017 August operation for breast cancer (no indications just an appointment came from BreastCheck through the Post). Trinity College Dublin Business Economics and Social Studies (but no degree) 1997-2003; UCD 1997/1998 night classes) essays, projects, writings. Trinity Horizon Programme 1997/98 (Centre for Women Studies Trinity College Dublin/St. Patrick's Foundation (Professor McKeon) EU Horizon funded: research study of 15 women (I was one of this group and it became the cornerstone of my journey to now 2017) over 9 mth period diagnosed with depression and their reintegration into society, with special emphasis on work, arts, further education; Notes from time at Trinity Horizon Project 1997/98; Articles written for Irishhealth.com 2003/2004; St Patricks Foundation monthly lecture notes for a specific period in time; Selection of Poetry including poems written by people I know; Quotations 1998-2017; other writings mainly with theme of social justice under the heading Citizen Journalism Ireland. Letters written to friends about life in Zimbabwe; Family history including Michael Comyn KC, my grandfather, my grandmother's family, the O'Donnellan ffrench Blake-Forsters; Moral wrong: An acrimonious divorce but the real injustice was the Catholic Church granting an annulment – you can read it and make your own judgment, I have mine. Topics I have written about include annual Brain Awareness week, Mashonaland Irish Associataion in Zimbabwe, Suicide (a life sentence to those left behind); Nostalgia: Tara Hill, Co. Meath.
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