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NHS gynaecology backlog reflects ‘grim’ underfunding and gender-biased neglect
Experts in England raise the alarm over the “deprioritisation” of women’s health

The NHS gynaecology backlog reflects “grim” underfunding and gender-biased neglect, experts have said, after new figures revealed that almost 600,000 women in England are waiting for gynaecological treatment.
New data has unveiled that 33,000 women in England are waiting more than a year for gynaecological treatment.
The research, which found that no region in England meets the government’s target for cervical cancer of 80 per cent coverage, has labelled the patchy access to cervical screening and gynaecological treatment as a “postcode lottery”.
Experts and women’s health campaigners, however, said the findings only reconfirm the “deeply worrying ” inequalities women are facing.
“The statistics sadly reinforce that gynaecological health is at the back of the queue,” Athena Lamnisos, CEO of leading gynae cancer charity The Eve Appeal, told Femtech World.
“We know that cervical cancer is a largely preventable disease, but to eliminate it in the UK we need to meet targets. We need to ensure everyone has accessible information about HPV and the benefits of vaccination to enable every young person to get vaccinated when it is offered to them.
“We need to make sure that everyone with a cervix has the information and support they need to access cervical screening, and to reduce the postcode lottery around the UK.”
Kate Muir, women’s health campaigner and author of Everything You Need to Know About the Pill, said: “The gynaecology backlog reflects grim underfunding and gender-biased neglect.
“Why is it acceptable to be left to bleed heavily and incomprehensibly for a year, to have a prolapsed womb, and just accept being incontinent when action can be taken?
“Just because these conditions are largely unseen and silent does not mean we should not be shouting about them and deserve care.”
The “excruciatingly long” wait times, Muir said, reflect a lack of joined up thinking in the NHS, where women are sent for GPs to clinics to specialists and back.
“The new one-stop-shop Women’s Health Hubs could make a huge difference – if only the government would properly fund them.”
Gynaecological conditions on the elective pathway are often perceived as less urgent than their counterparts in other surgical specialties.
However, while waiting, women are left struggling with symptoms, such as extreme pain, heavy menstrual bleeding and incontinence. Long waits can also result in more complex treatment needs or emergency admission to hospital.
The Royal College of Obstetricians and Gynaecologists (RCOG) estimates that nearly nine in ten (89 per cent) healthcare professionals think gynaecology waiting times are impacting patients’ quality of life.
Bridget Little, head of support services at Jo’s Cervical Cancer Trust, said screening and early intervention could save lives.
“Two women are dying every day in the UK from a cancer that is largely preventable, yet the vast disparities in access to cervical screening, and the unmet coverage targets seen across the UK, are deeply concerning.
“We have an incredible opportunity to eliminate cervical cancer in the UK within a generation, but this will only be realised with effective strategies that recognise and rectify the widespread health inequalities across the UK.”
Little said urgent measures must be implemented to ensure that everyone who is eligible has fairer access to cervical screening and that all patients who need treatment for cervical cell changes receive the right treatment at the right time.
“It is vital that the government firmly commits to tackling health inequalities, and to providing appropriately resourced NHS services,” she added.
Venkatesh Subramanian, consultant in obstetrics, gynaecology and reproductive medicine at King’s College Hospital, said: “Currently, the UK has the largest gender health gap in the G20, which is deeply worrying.
“Gender inequalities in healthcare need to be aggressively challenged, with a comprehensive strategy focusing on improved allocation of resources and funding, prioritisation of research and development in the field and an end to the stigma and paternalism that enshrouds women’s healthcare.”
Dr Nitish Narvekar, fertility consultant at King’s Fertility and clinical director gynaecology at King’s College London, acknowledged the “distressing” health inequalities, but argued that the pandemic is also to blame for the long NHS waiting times.
“We know, for example, that some NHS organisations had to allocate resources based on greatest need and which may have disproportionately impacted those who are relatively ‘healthy’ but nevertheless suffer in other ways from waiting longer,” he explained.
“The NHS is responding to the challenges in different ways. For example, care is increasingly being organised and delivered sector-wide rather than just at level of individual organisations.
“However, patients will continue to be affected till all the service-delivery issues are resolved locally and nationally.”
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Endometriosis documentary profiles stars including Marilyn Monroe and Amy Schumer

A non-profit has launched an endometriosis documentary featuring Amy Schumer and Marilyn Monroe as it pushes for changes in how the condition is treated and understood.
The Endometriosis Collective has launched to change how endometriosis is researched, treated and understood, starting with a documentary featuring stories from people including Amy Schumer and Marilyn Monroe.
The feature-length documentary, “End of the Cycle”, will premiere in New York on Tuesday, and The Endometriosis Collective is making the film free to stream online.
Schumer, a comedian, writer and actor, has previously spoken of how endometriosis left her “on the floor in pain, vomiting from the pain, the pain that nobody can see.”
Schumer is one of several celebrities featured in the documentary. Other contributors include dancer Julianne Hough, Olympic medallist Brittany Brown and actors Janel Parrish and Folake Olowofoyeku.
The Endometriosis Collective timed the documentary premiere to coincide with the 100th anniversary of Marilyn Monroe’s birth.
Monroe, who died in 1962, starred in films such as “Some Like It Hot” and “Gentlemen Prefer Blondes.”
According to a biography published in 1985, Monroe’s endometriosis was so severe that it destroyed her marriages, her wish for children, her career and ultimately her life.
The Endometriosis Collective said the documentary shares newly uncovered information about Monroe’s experience with endometriosis.
The non-profit said the information connects Monroe’s story to the experiences of women across generations, highlighting how far awareness, research and care still have to go.
A representative of the Marilyn Monroe Estate said: “By sharing this part of her story through ‘End of the Cycle,’ we hope to honour her legacy in a way that brings visibility to endometriosis, encourages more open dialogue and helps inspire the research needed to create change.”
As part of the premiere, The Endometriosis Collective is holding a panel discussion.
Schumer, Brown and Olowofoyeku, the documentary’s co-directors Sammy Jaye and Soraya Simi, and medical experts are due to be part of the premiere.
AbbVie’s Orilissa and Sumitomo Pharma’s Myfembree are among the approved drugs for endometriosis pain.
Hough, one of the participants in the documentary, starred in an Orilissa campaign in 2017.
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