logo
Trans activists urge doctors to fight NHS data overhaul

Trans activists urge doctors to fight NHS data overhaul

Telegraph01-04-2025

Trans activists are urging NHS staff to campaign against plans to protect women by collecting data on sex and not gender.
They have posted on NHS England's LGBT intranet to implore doctors and nurses to show their 'allyship' by writing to their MP to oppose the proposed changes.
In a report last month, Professor Alice Sullivan said police forces and the NHS should collect data on biological sex rather than a person's self-declared gender identity.
Critics say that allowing public bodies to remove sex from statistical records compromises research into women's issues and makes it difficult for researchers to spot trends in rape cases, medical trials or gender pay gaps.
Professor Sullivan's review found that cancer referrals had been missed and previous convictions overlooked because biological sex was not being recorded.
The report was welcomed by Wes Streeting, the Health Secretary, who said having accurate data on sex was vital for patient safety.
But activists have described it as 'biased, inadequate and potentially harmful'.
'Demonstrate your allyship'
In a post on NHS England's LGBT network, one activist linked to a statement from the group TransActual which rejected the report.
The post said: 'Leading transgender organisation TransActual together with academics from the Feminist Gender Equality Network (FGEN) today rejected the conclusion of a report on data collection by academic Professor Alice Sullivan as biased, inadequate and potentially harmful to all citizens of the UK, whether trans or not.
'For allies within the network, now is the time to take action. Demonstrate your allyship by writing to your local MP and urging them to oppose the recommendations of the report.
'Encourage them to speak out against it within their party and advocate for a more inclusive approach.'
The activist then linked to TransActual's statement on the Sullivan Review, which claimed the idea that there are only two sexes is 'factually incorrect' and an 'incorrect dog-whistle assertion'.
It also said Professor Sullivan was a 'prominent anti-trans activist'.
Its strategy director, Keyne Walker, said: 'These recommendations would do nothing to support the Government's stated objectives regarding equality and diversity, nor on data use. It represents a deviation from the Government's stated position, and would be a U-turn should it be implemented.
'Worse, the experience of those working in the field suggests that far from improving data quality, the measures promoted by this report would make data collected on sex and gender far less reliable.
'The Sullivan Review is rooted in factually incorrect assertions about the binary nature of sex and gender and antipathy towards trans people, despite lip-service towards respect for diverse gender identities.
'The Review's recommendation for both sex and gender characteristics to be collected is presented as in the interest of the welfare of trans people.
'However, the recommendations would effectively mean that trans people have no right to privacy, likely breaching human rights law, as well as codifying the incorrect dog-whistle assertion that sex is binary and immutable.'
She went on: 'Despite its claims of impartiality, it was produced by leading members of an anti-trans campaign group and reflects their arguments.
'As such, it is an unsuitable basis for policymaking and we encourage DSIT to reject its findings entirely.'
Fiona McAnena, director of campaigns at women's rights charity Sex Matters, said the comments showed why Mr Streeting needed to 'get gender ideology out of the health service'.
She said: 'It is shocking to see an NHS England employee amplifying calls from a trans activist group to ignore the recommendations of the Sullivan report.
'This should be a wake-up call to the [Health Secretary] to get gender ideology out of the health service, for everyone's sake.
'Whether a patient is male or female is vital information in healthcare, but this lobby group wants the NHS to record falsehoods instead of facts in people's health records. This is not good for anyone. It's no longer credible to claim that trans activist demands are no threat to anyone else.'
A spokesman for NHS England did not comment on the campaign against the adoption of Prof Sullivan's recommendations.
He said: 'The NHS has written to GPs to ensure that they immediately stop the process of changing NHS numbers and gender markers for children and young people under 18, following the Sullivan review and the Secretary of State for Health and Social Care's direction.'

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Psychological support system opens to infected blood victims
Psychological support system opens to infected blood victims

Rhyl Journal

time31 minutes ago

  • Rhyl Journal

Psychological support system opens to infected blood victims

The nationwide service began a phased rollout in September, and is now open to people infected and affected across the country. The Infected Blood Psychological Service will include talking therapies; peer support and psychosocial support, NHS England said. More than 30,000 people in the UK were infected with HIV and hepatitis C after they were given contaminated blood and blood products between the 1970s and early 1990s. And more than 3,000 people have died as a result, while survivors are living with lifelong health implications. The new service is open to victims of the scandal as well as bereaved partners, parents, children and their extended families. People can self refer by phone or can be referred to the service by their GP. Officials said that a specialist therapist will help create tailored mental health plans for those in need of support. The Infected Blood Inquiry Report is now published on the Inquiry website. Access the Report here: — Infected Blood Inquiry (@bloodinquiry) May 20, 2024 Claire Murdoch, national mental health director at NHS England, said: 'The contaminated blood scandal and the subsequent long fight for answers have had life-altering physical and psychological impacts for thousands across the country and the NHS is determined to ensure that anyone infected or affected can receive evidence-based support and treatment. 'It has been so important that the Infected Blood Psychological Service has been co-designed with members of the infected blood community to ensure the best and most personalised care possible, and we are very grateful to all our partners who have helped establish these vital new services.' Nicola Leahey, from Lancashire, was infected with Hepatitis C following blood transfusions in 1975 and/or 1980, and was part of the expert advisory group to the new service. 'After my diagnosis, I felt that my body had been violated, that I had been physically and mentally abused, stripped of my dignity, my self-esteem diminished, I mourned lost opportunities, I felt betrayed,' she said. 'So many of us have long awaited the opportunity to have professional support to try to cope with the trauma and life-long effects that we've been subjected to. 'I'm thrilled that this much-needed service is now operational for both those infected and affected members of the infected blood community across England.' Professor Meghana Pandit, co-national medical director for secondary care at NHS England, added: 'Following the recommendations of the Inquiry, this new service represents a vital step in ensuring patients and families affected in England can be offered tailored psychological treatment and support, and we are pleased that specialist clinics are now open in all areas of England. 'This bespoke psychological treatment is already making a difference to the lives of the first people to access it, and we now want to ensure everyone eligible is aware of the services provided.'

Psychological support system opens to infected blood victims
Psychological support system opens to infected blood victims

Glasgow Times

time32 minutes ago

  • Glasgow Times

Psychological support system opens to infected blood victims

The nationwide service began a phased rollout in September, and is now open to people infected and affected across the country. The Infected Blood Psychological Service will include talking therapies; peer support and psychosocial support, NHS England said. More than 30,000 people in the UK were infected with HIV and hepatitis C after they were given contaminated blood and blood products between the 1970s and early 1990s. And more than 3,000 people have died as a result, while survivors are living with lifelong health implications. The new service is open to victims of the scandal as well as bereaved partners, parents, children and their extended families. People can self refer by phone or can be referred to the service by their GP. Officials said that a specialist therapist will help create tailored mental health plans for those in need of support. The Infected Blood Inquiry Report is now published on the Inquiry website. Access the Report here: — Infected Blood Inquiry (@bloodinquiry) May 20, 2024 Claire Murdoch, national mental health director at NHS England, said: 'The contaminated blood scandal and the subsequent long fight for answers have had life-altering physical and psychological impacts for thousands across the country and the NHS is determined to ensure that anyone infected or affected can receive evidence-based support and treatment. 'It has been so important that the Infected Blood Psychological Service has been co-designed with members of the infected blood community to ensure the best and most personalised care possible, and we are very grateful to all our partners who have helped establish these vital new services.' Nicola Leahey, from Lancashire, was infected with Hepatitis C following blood transfusions in 1975 and/or 1980, and was part of the expert advisory group to the new service. 'After my diagnosis, I felt that my body had been violated, that I had been physically and mentally abused, stripped of my dignity, my self-esteem diminished, I mourned lost opportunities, I felt betrayed,' she said. 'So many of us have long awaited the opportunity to have professional support to try to cope with the trauma and life-long effects that we've been subjected to. 'I'm thrilled that this much-needed service is now operational for both those infected and affected members of the infected blood community across England.' Professor Meghana Pandit, co-national medical director for secondary care at NHS England, added: 'Following the recommendations of the Inquiry, this new service represents a vital step in ensuring patients and families affected in England can be offered tailored psychological treatment and support, and we are pleased that specialist clinics are now open in all areas of England. 'This bespoke psychological treatment is already making a difference to the lives of the first people to access it, and we now want to ensure everyone eligible is aware of the services provided.'

Women with genetic cancer risk being ‘missed' due to testing gaps
Women with genetic cancer risk being ‘missed' due to testing gaps

Leader Live

timean hour ago

  • Leader Live

Women with genetic cancer risk being ‘missed' due to testing gaps

A lack of testing for Lynch syndrome also means some cancer patients are unaware of their risk of developing other cancers, academics said. Lynch syndrome is a rare condition which runs in families which puts people at a higher risk of developing cancers of the bowel, womb and ovaries. It is caused by a mutation in the gene that fixes mistakes in DNA when it is copied, which can lead to uncontrolled cell growth. Patients with bowel or womb cancer should have their tumours assessed for markers of Lynch syndrome, according to guidance for the NHS. If these markers are identified, patients should be referred for genetic testing so the diagnosis can be confirmed and they can get support and advice about cancer risk for themselves and their family. A new study by academics at the University of Edinburgh found not all womb cancer patients are being sent for genetic testing. Researchers examined data on 2,500 womb cancer patients across the UK and Ireland between 2022 and 2023. We have launched a Guide to #LynchSyndrome to help provide information and support to anyone who thinks they may have it, that it may run in the family, or have found out they have — The Eve Appeal (@eveappeal) February 13, 2023 They found that 91% of tumours were tested for markers of Lynch syndrome, but the test results were not routinely communicated to the wider clinical team. This means that follow-up genetic counselling and blood tests were not always arranged. Of the 181 participants eligible for genetic counselling, just under two-thirds (64%) were referred for appointments, according to the study, which has been published in the journal BMJ Oncology. Researchers said those who were referred faced long waits, resulting in high dropout rates, meaning only 48% of those eligible went on to get the test. Today's #LynchSyndromeAwarenessDay. Our policy team sat down with our supporter, Jane, to share her experience. As well as highlighting what else needs to be done to improve Lynch syndrome care. Read our blog: — Bowel Cancer UK (@bowelcanceruk) March 22, 2025 Experts from the university said gaps in testing mean some womb cancer patients with Lynch syndrome go undetected. Family members are also left vulnerable to cancer risk, unaware they may have the condition. Dr Neil Ryan, from the University of Edinburgh, who leads the UK audit and research collaborative in obstetrics and gynaecology, said: 'Despite clear guidance and excellent rates of tumour testing, too many women with Lynch syndrome are still being missed because they're not referred for definitive blood testing in a timely way. 'This not only denies them the chance to reduce their future cancer risk but also prevents their relatives from being tested and protected. 'Tumour testing is only cost-effective if it leads to diagnosis — we urgently need to make mainstream testing truly mainstream.'

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into the world of global news and events? Download our app today from your preferred app store and start exploring.
app-storeplay-store