Category Archives: Endometriosis

Ultrasound diagnosis could lead to faster treatment of endometriosis

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New guidelines call for non-invasive test methods to be offered to patients to avoid long waits for surgical diagnosis

People showing symptoms of endometriosis should be offered diagnosis options such as ultrasound so they receive treatment sooner, according to updated guidelines.

Endometriosis can take years to be diagnosed, as it has previously meant waiting for a surgical procedure to make the diagnosis.

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Daily endometriosis pill approved for NHS could help 1,000 women a year

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Linzagolix hailed as a possible ‘gamechanger’ in tackling the painful condition for some patients in England

More than 1,000 women a year in England could benefit from a new pill for endometriosis.

The condition occurs when tissue similar to the womb lining grows elsewhere in the body, such as the pelvis, bladder and bowel. It can cause chronic pain, heavy periods, extreme tiredness and fertility problems.

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People with endometriosis more likely to experience early menopause, study finds

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Surgical menopause occurs on average 19 months earlier, while natural menopause happens five months earlier, new global research shows

Women with endometriosis face a higher risk of premature and early menopause and are seven times more likely to experience surgical menopause, a study has found.

Surgical menopause occurs when a woman has both ovaries removed before reaching natural menopause, and may be done to treat endometriosis if other treatments fail.

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One in four women in England have serious reproductive health issue, survey finds

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Exclusive: Racial disparities highlighted as researchers estimate 10 million women have conditions such as fibroids or endometriosis

More than a quarter of women in England are living with a serious reproductive health issue, according to the largest survey of its kind, and experts say “systemic, operational, structural and cultural issues” prevent women from accessing care.

The survey of 60,000 women across England in 2023, funded by the Department of Health and Social Care and analysed by academics at the London School of Hygiene & Tropical Medicine, found that 28% of respondents were living with a reproductive morbidity, such as pelvic organ prolapse, uterine fibroids, endometriosis, polycystic ovary syndrome, or cervical, uterine, ovarian or breast cancer.

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Women to save thousands of dollars a year as new fertility and endometriosis drugs listed on PBS

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New contraceptives, IVF and endometriosis treatments added to federal subsidy scheme, with Coalition leaders backing the move

New medications related to contraception, endometriosis and IVF will be subsidised on the Pharmaceutical Benefits Scheme (PBS) from 1 May, with some women expected to save thousands of dollars each year.

The announcement from the federal government on Sunday was welcomed by health campaigners, who said women’s health issues have been sidelined for far too long.

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‘Women are suffering unnecessarily’: Australians to get subsidised endometriosis treatment

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Without a subsidy, patients could pay $750 a year to treat the condition which has no cure and can last decades

More than one million Australians living with endometriosis will have access to a treatment subsidised by the federal government for the first time in three decades.

The health minister, Mark Butler, announced on Sunday that a daily tablet will be listed on the Pharmaceutical Benefits Scheme (PBS).

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Canberra Health Services apologises for video that left endometriosis advocates ‘appalled’

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ACT government organisation deletes video that said endometriosis and arthritis were not conditions appropriate for emergency department

Canberra Health Services has removed a video it acknowledged was “not well executed and open to misinterpretation” after “appalled” advocates of endometriosis accused the government organisation of diminishing the acute pain of people living with endometriosis and arthritis.

The video, intended to provide an overview of how emergency departments worked as part of a larger health literacy campaign, has since been deleted from Canberra Health Services’ Instagram account. It is still visible on ABC News.

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A year on, Spain’s ‘historic’ menstrual leave law has hardly been used. Why?

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Women in Spain have the right to time off work with period pain, but limits in the legislation and lack of awareness mean few have taken it

It was hailed as a historic advance – one capable of tackling longstanding workplace taboos around period pain. A year after Spain became the first country in Europe to introduce paid menstrual leave, however, figures suggest that relatively few employees have made use of the policy.

In the 11 months since the law was introduced, menstrual leave was taken 1,559 times, according to data from Spain’s ministry of inclusion, social security and migration.

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Kate has endometriosis – and gastro problems. New research shows she’s not alone

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Genetic links have been revealed between the crippling chronic condition and painful gastrointestinal disorders

After 16 rounds of surgery for endometriosis, Kate Fisher underwent a hysterectomy at age 34.

She thought it would mean an end to the debilitatingly painful periods – instead, she began shedding from her bowel each month.

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Australia news live: Central Land Council executive condemns Jacinta Price’s ‘denial of history’ in press club comments as ‘disgraceful’

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The CLC executive – 90 elected members who represent 75 communities across nine regions – said comments insult survivors of 1927 Coniston massacre. Follow the day’s news live

New report combats ‘inaccurate assertions’ about teaching courses

Almost three-quarters of Australian teachers are satisfied with their training programs, a new report has found, undermining the suggestion poor course content is leading to workforce shortages in the field.

Rather than focusing on the unsubstantiated claim that teachers are generally dissatisfied with ITE programs, we should instead focus on the willingness and capacity of ITE providers to continually improve these programs.

This will require a shift in focus from policymakers - away from the overwhelming emphasis on ITE and towards effective, system-wide [development] that becomes a regular part of teachers’ workload rather than a bolt-on.

Not a preamble. Not a footnote in the Constitution. First Nations people want structural change that can make a practical difference.

A mechanism that can make children’s lives better. Not just something that will feel good - something that will do good.

As the Minister, I will go to the voice and say: ‘this school attendance program isn’t working’. Help me to get the best possible advice to fix it … From every corner of the country – about how we can do better.

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Sufferers of chronic pain have long been told it’s all in their head. We now know that’s wrong

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In the first of a series looking at chronic pain and long Covid, Linda Geddes explores the growing realisation that pain can be a disease in and of itself – and the pandemic could be making it worse

It started with headaches and neck pain, but no sooner had Tricia Kalinowski’s physiotherapist come up with a strategy to tackle these problems, then another area of her body would start to hurt: her lower back, her hip or her jaw.

“The physio was chasing the pain up and down my body,” says Kalinowski, 60, from Minneapolis, US. Eventually, she was referred to an oral surgeon, who believed the root cause of these issues was a problem with one of the joints in her jaw, so she underwent surgery to replace a thumbnail-sized disc.

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‘Disgusting’ study rating attractiveness of women with endometriosis retracted by medical journal

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Fertility and Sterility took seven years to take down Italian study, which was criticised by doctors for ethical concerns and dubious justifications

A widely criticised peer-reviewed study that measured the attractiveness of women with endometriosis has been retracted from the medical journal Fertility and Sterility.

The study, Attractiveness of women with rectovaginal endometriosis: a case-control study, was first published in 2013 and has been defended by the authors and the journal in the intervening years despite heavy criticism from doctors, other researchers and people with endometriosis for its ethical concerns and dubious justifications, with one advocate calling the study “heartbreaking” and “disgusting”.

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