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Barratts/S&G Barratts/EMPICS Archive

Column Symphysiotomy was seen as a gateway to childbearing without limits

Chairperson of Survivors of Symphysiotomy, Marie O’Connor explains how women’s pelvises were unhinged to avoid Caesarean section, which was disliked by Catholic hospitals because of its association with “the crime of birth prevention”.

SYMPHYSIOTOMY IS A cruel and dangerous childbirth operation that unhinges the pelvis, severing the symphysis joint or, in the case of pubiotomy, sundering the pubic bones.

Ireland was the only country in the developed world to practise this discarded surgery in the mid to late 20th century.

Caesarean section had been the standard treatment for difficult births in Ireland since the end of the 1930s. However, doctors’ preference for symphysiotomy saw 1,500 of these 18th century operations being performed from 1944 onwards, mostly in Catholic private hospitals. Around 150 women survive today, many of them permanently disabled, incontinent and in pain. One baby in ten died during the process and a number were brain damaged.

Women were occasionally informed their pelvis would be broken, but most were not.

Some believed they were going to have a Caesarean section. Others were symphysiotomised under general anaesthetic during pregnancy, or, as in Olivia Kearney’s case, to ‘deliver’ a baby already born by Caesarean.

The majority, however, were left for many hours in the labour ward before being operated upon, wide awake, without their consent. One woman described the wire saw used to cut her pubic bone as being ‘like broken glass’, tearing into her.

Push through the agony

After the surgery, women were still in labour. Sometimes the baby took hours, or days, to come; then they had to push for as long as it took, through the agony of an unhinged pelvis. In one case, where the baby was in a brow position– incompatible with vaginal birth– it took four hours of ‘maternal effort’ to get the baby out. Those unable to give birth vaginally were eventually given the Caesarean section that had earlier been withheld.

Instead of nursing women as surgical patients, midwives further destabilised the severed bone or joint by forcing women to walk on their broken pelvises, often within a day or two of giving birth. Some fainted from the pain. Discharged from hospital without medical advice or painkillers, women were sent home to sink or swim. Many never recovered.

The surgery was an abuse of power, a pre-emptive surgical strike against the practice of birth control by obstetricians who disliked Caesarean section, on account of its association with what Archbishop McQuaid termed the ‘crime of birth-prevention’. Undergoing four such operations was widely seen as the upper safety limit. Symphysiotomy, in contrast, was viewed as a gateway to childbearing without limitation.

Long shunned by doctors on account of its dangers, symphysiotomy was revived in 1944 at Holles St Hospital as a replacement for Caesarean section in certain cases. Pregnant women were used as guinea pigs there in the 1940s and ’50s and this experimentation reached bizarre heights at the Lourdes Hospital, Drogheda, then under the ownership of the Medical Missionaries of Mary.

False claims of ‘unsafe’ Caesarean sections

Women were also used as clinical material to train staff bound for overseas. One woman reported seeing a camera in the operating theatre at the Lourdes Hospital just before she lost consciousness. The low cost operation was seen as invaluable, especially for trainees from developing countries, in hospitals that aimed to become international training centres.

Regulatory failure allowed the practice of this mutilating surgery for half a century. Hospital reports detailing these operations were ignored.

False claims that Caesarean section was unsafe until the 1960s and that symphysiotomy was performed for medical reasons are still being made.

Official briefs continue to reflect the myths propagated by the Department of Health, which has allowed itself to be captured by the body whose members committed these atrocities, namely, the Institute of Obstetricians and Gynaecologists.

The courts represent survivors’ sole route to truth and justice. But actions that are brought outside the time limit (two years since 2004) cannot succeed. The clock runs from the time that you become aware that your injuries resulted from wrongdoing or negligence. In some cases, the date of that knowledge is unclear. These were covert operations: three or four decades elapsed in most cases before women understood that their pelvises had been broken. Many were having a first baby, and knew nothing about childbirth. All of them, without exception, assumed, or were told, that whatever was done was necessary to save the life of the baby. The medical profession closed ranks, in general. Few admit any connection between women’s ill-health and their symphysiotomies.

The knowledge that this was wrongful surgery came slowly and painfully, in fragments heard in the media or read in a newspaper. Accepting that one has been abused is difficult: denial is easier.

Ms Kearney’s case was initially dismissed in the High Court on the grounds of undue delay. Now that the veil has been rent on these abusive operations, the Oireachtas should lift the statute of limitations for survivors, for a brief period. This was done for victims of sexual abuse, a far more difficult area to legislate for. There are no floodgates, only 130 or so mainly elderly women, standing, waiting, for justice.

Marie O’Connor is the author of Bodily Harm: symphysiotomy and pubiotomy in Ireland 1944-92′ and the chairperson of Survivors of Symphysiotomy, the support group for victims of the practice.

Dáil hears calls for justice for survivors of symphysiotomy>

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63 Comments
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    Mute Elena R
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    Feb 28th 2025, 4:18 PM

    Incredible group of parents, thank you for advocating for our beautiful children

    179
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    Mute Lei tatt
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    Feb 28th 2025, 4:30 PM

    @Elena R: FFG over and over failing Irish children

    109
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    Mute Gerry Kelly
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    Feb 28th 2025, 5:02 PM

    Children start school here at 4 or 5 years of age. We have a census every 5 years, so the statistics are there for how many children need school places, and how many have extra/special needs.
    And yet this issue has been ongoing not for years but decades.
    If you judge a society by how it treats its weakest and most vulnerable then in this regard our republic is a miserable failure, and shame on successive Education ministers and their civil servants

    99
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    Mute Brian Molloy
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    Feb 28th 2025, 5:05 PM

    Would love to know how many of these parents voted for ffg in the recent election

    61
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    Mute James Smith
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    Feb 28th 2025, 5:07 PM

    @Brian Molloy: none of them. When you are knee deep in battling the government every day for your basic rights, you tend not to vote for the incumbent government.

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    Mute Peter Sponge
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    Feb 28th 2025, 5:16 PM

    @James Smith: you’ll get a woeful boot up the hole if the others get in lol

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    Mute sean weir
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    Feb 28th 2025, 5:16 PM

    @Brian Molloy: most of them probably, people in this country don’t like change,good or bad

    29
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    Mute Matt D
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    Feb 28th 2025, 5:20 PM

    @Brian Molloy: parents of children with additional & complex needs are often easy prey to the promises of politicians. As a father of 2 kids with autism I know the struggles & the fears. Politicians simply do not care one bit for us & our children.

    52
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    Mute James Smith
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    Feb 28th 2025, 6:22 PM

    @Peter Sponge: like the boot in the hole parents are currently getting off the incumbents. Your comment just doesn’t make sense.

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    Mute Terence Maxwell
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    Feb 28th 2025, 6:30 PM

    @Brian Molloy: the people of Ireland vote for them,

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    Mute Loulou
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    Mar 1st 2025, 2:08 AM

    @Peter Sponge: another feckin dope is what you are.

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    Mute paul ruddell
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    Feb 28th 2025, 4:42 PM

    Bigger fool, anyone who believes the Irish government care about these kids.
    At the stroke of a pen, a magic money tree appeared for Covid, then Ukraine, then pet projects eg bike shed, children’s hospital and self pay increases. Yes hard work will be involved in correcting these issues for the families, and unfortunately the Gov only put in the hard yards for cover ups.

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    Mute sakk sa
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    Feb 28th 2025, 5:21 PM

    @paul ruddell: The government will never do enough to support children with special needs or speech delays. Schools may be willing to help by hiring specialized teachers or assistants, but only if funding is provided. Meanwhile, the HSE (Health Service Executive) continues to neglect these children, leaving them on waiting lists for months—or even years.

    Time is critical. Every day matters when a child needs speech therapy or a diagnosis. Delays in intervention cause irreversible damage, and once that damage is done, it becomes permanent. This permanence creates lifelong struggles for the child, and parents—along with every family member—are left to shoulder the burden alone. While parents and families fight tirelessly, becoming unsung heroes, the government remains detached, seemingly unaware of the depth of their suffering.

    As a parent, I urge others to remember this: Screens and mobile devices cannot replace genuine human interaction and active engagement. Prioritize real communication and meaningful activities—they make all the difference.
    I agree with your say

    58
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    Mute Jacintha Dumbrell
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    Feb 28th 2025, 5:40 PM

    Every single person who gave Fine Gael and Fianna Fáil a vote, this is on you, and the record homelessness numbers this month.

    36
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    Mute Loulou
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    Mar 1st 2025, 2:05 AM

    @Jacintha Dumbrell: up yours you haven’t a clue with your flippant comments

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    Mute j m m
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    Mar 1st 2025, 9:56 AM

    @James Fields: on at 3.30am with new account…. berating parents with special needs kids? What’s it like being you?

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    Mute Oh Mammy
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    Feb 28th 2025, 5:09 PM

    These parents are so selfish. Don’t they know we need fighter jets?

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    Mute Mary Kelly
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    Feb 28th 2025, 7:22 PM

    A billion spent on aslyum seeker accommodation last year, a hundred thousand euro spent yesterday on deporting 30 people. The money is there but it is being spent on other things to keep the EU happy.
    All in the name of protecting the vulnerable, yet truely vulnerable aslyum seekers are lost in the mass, while money being spent on free accommodation but the most vulnerable of our society, children with additional needs cannot be supported or educated in the country they were born and their tax paying parents cannot get support. This is insane, people say voting for fffg, but the opposition would still spend the money, look at social democrats who came out today denouncing the deportations and lack of aslyum accommodation,

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    Mute Peter Sponge
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    Feb 28th 2025, 4:47 PM

    Loudmouth Barrett, he would be happy to flood the country with Islamists

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    Mute sean weir
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    Feb 28th 2025, 5:14 PM

    @Peter Sponge: that’s it you deflect as much as you can

    36
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    Mute j m m
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    Feb 28th 2025, 5:22 PM

    @Peter Sponge: Reported you but in the meantime, maybe spend 2 mins thinking about this 1 of your million dum comments. You’ve attempted to antagonise and provoke folks about kids with special needs? You lo lyfe sk-um nugget. Get help.

    36
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    Mute j m m
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    Mar 1st 2025, 8:45 AM

    @James Fields: Peter, jim, dave… you awake? If p .Sponge is already deleted, then I’ll just come after “james” and all your accounts. But seriously, are you paid to troll here? If not, then listen to everyone who tells you….. you need help.

    2
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    Mute Rosie Martin
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    Feb 28th 2025, 5:23 PM

    @Peter Sponge: Clearly you know nothing about disability, highly offensive and ignorant comment. Stand with families who have kids with disabilities rather than such ignorance.

    42
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    Mute Tony O'Toole
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    Feb 28th 2025, 4:19 PM

    Does she not know what their concerns are. Typical of her,as usual .

    16
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    Mute sakk sa
    Favourite sakk sa
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    Feb 28th 2025, 5:19 PM

    The government will never do enough to support children with special needs or speech delays. Schools may be willing to help by hiring specialized teachers or assistants, but only if funding is provided. Meanwhile, the HSE (Health Service Executive) continues to neglect these children, leaving them on waiting lists for months—or even years.

    Time is critical. Every day matters when a child needs speech therapy or a diagnosis. Delays in intervention cause irreversible damage, and once that damage is done, it becomes permanent. This permanence creates lifelong struggles for the child, and parents—along with every family member—are left to shoulder the burden alone. While parents and families fight tirelessly, becoming unsung heroes, the government remains detached, seemingly unaware of the depth of their suffering.

    As a parent, I urge others to remember this: Screens and mobile devices cannot replace genuine human interaction and active engagement. Prioritize real communication and meaningful activities—they make all the difference.

    12
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    Mute Tony O'Toole
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    Feb 28th 2025, 4:22 PM

    Does she not know what their concerns are. Typical of her. As usual .

    9
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    Mute Ed Brennan
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    Mar 1st 2025, 10:52 AM

    Lots of money and accommodation for those who don’t like us very much, but not for Irish children.
    Sure we’re a great country.

    7
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    Mute UNA NI MHATHUNA
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    Feb 28th 2025, 10:49 PM

    Sadly this is not new news and each government have been fully aware of this ÿou need a country wide march with families standing together shake the core of them to their utter shame

    6
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    Mute DAN TEDSON
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    Mar 1st 2025, 8:15 AM

    HSE have loads of managers to compile reports and do assessments. But have rarely met any speech or occupational therapy people for my kid. The field is exclusively women and many go on maternity leave and never return. Or take years off for sabbaticals. Work life balance is great, but we need more people in general in these services and we need it to be gender balanced.

    3
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    Mute Pat Redmond
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    Mar 1st 2025, 10:45 PM

    @DAN TEDSON: fathers can take sabbaticals too.

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    Mute Peter Sponge
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    Feb 28th 2025, 10:10 PM

    Badly behaved kids, a good clip round the ear is needed

    4
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    Mute j m m
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    Mar 1st 2025, 1:11 AM

    @Peter Sponge: dear journal, can’t you delete anything that comes from this degenerates ip address?

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    Mute Giulia Fancelli Clifford
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    Mar 1st 2025, 5:45 PM

    Yeah, I totally agree. Tell me about it. I had to apply to 43 schools to secure a secondary school place in an ASD class for my son, balancing this with full-time work. Despite schools offering online applications for neurotypical students, many demand paper applications for ASD places, forcing me to deliver 12 applications personally. My husband even took a day off work for this nonsense. We’ve had to pay for everything—OT, speech therapy, private tuition, educational assessment—you name it. While the NDT shifts responsibility to parents after a one-hour course. The state offers just 40 summer tuition hours, and HSE assessments are inaccessible. Meanwhile, Sensational Kids faced roadblocks in opening a new Kildare assessment centre. The system is failing our kids.

    2
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    Mute DAN TEDSON
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    Mar 1st 2025, 8:15 AM

    T-h-e-r-a-p-i-s-t is a banned word on this platform?

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