Daily Mail

Doctors take a year longer to spot endometrio­sis

- By Shaun Wooller Health Editor

WOMEN must wait almost a year longer to be given an endometrio­sis diagnosis than before the pandemic, a report reveals.

it now takes an average of eight years and ten months for doctors to identify the painful disease, an increase of ten months since 2020.

Most women made at least one visit to A&e and almost half needed ten or more GP appointmen­ts before being diagnosed.

the waits delay access to treatment, when the disease can progress, leading to a risk of permanent organ damage. charity endometrio­sis UK said women were being ‘dismissed, ignored and belittled’. endometrio­sis affects the physical and mental health of one in ten women in the UK from puberty to menopause, though the impact may be felt for life, the charity added.

in sufferers, cells similar to the ones in the lining of the womb are found outside the uterus. each month these cells react in the same way to those in the womb, building up and then breaking down and bleeding.

Unlike the womb cells that leave the body as a period, they have no way to escape.

the new endometrio­sis UK report, based on a survey of 4,371 women with the disease, highlights a rise in diagnosis times in all four UK nations since 2020.

Almost half of all respondent­s (47 per cent) had visited their GP at least ten times with symptoms prior to receiving a diagnosis. Only 10 per cent said that GPs mentioned they suspected endometrio­sis at their first or second appointmen­t.

some 52 per cent had visited A&e at least once, and fewer than a fifth of these (17 per cent) were referred to gynaecolog­y at their first visit. More than quarter (26 per cent) of respondent­s visited A&e three or more times with symptoms prior to diagnosis. And 20 per cent reported seeing a gynaecolog­ist ten or more times before being diagnosed. Remarkably, 78 per cent of those who were later diagnosed were told they were making a ‘fuss about nothing’.

the disease affects 1.5 million women in the UK but endometrio­sis UK says is not allocated sufficient resources.

Women’s health strategy minister Maria caulfield said: ‘We are working to turn dismissed, ignored and belittle into listened to, understood and empowered.’

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