Women can wait years for an endometriosis diagnosis. New tech could change that

Key developments are emerging from the global stage. Women can wait years for an endometriosis diagnosis. New tech could change that 5 hours ago Share Save Add as preferred on Google Smitha Mundasad Health reporter Getty Images For thousands of women, getting an endometriosis diagnosis can take years. Now, a new scan technique may help spot the condition earlier, a pilot study at Oxford University suggests.

The technique uses CT scans combined with a molecular tracer to detect areas of early endometriosis, which is often missed by conventional scans. If confirmed in larger studies, this could help give women an explanation for their symptoms earlier on, scientists say. Endometriosis affects one in 10 women in the UK and is often a painful condition in which cells similar to those lining the womb grow elsewhere in the body.

The Details

It can take an average of nine years to get a diagnosis. Symptoms can be severe and wide-ranging - from very heavy periods to extreme tiredness and abdominal pain - often mimicking other conditions. People frequently end up undergoing several tests, including ultrasounds and sometimes MRI scans.

But these standard scans do not always pick up on the disease and mainly detect changes that often appear with more advanced diseases, says Dr Tatjana Gibbons, lead researcher on the study. "This means many struggle with symptoms, despite being told they have normal imaging results. "Getting a diagnosis earlier can help people make decisions and plans about their life," Dr Gibbons adds.

'A very long journey' Gabriella Pearson, co-founder of the charity Menstrual Health Project, was diagnosed with endometriosis aged 23, after more than 10 years of worsening symptoms and a number of misdiagnoses. The 33-year-old says that if she had been "listened to and diagnosed earlier she would have been in a very different position now". Gabriella Pearson It took 10 years for Gabriella Pearson, 33, to be diagnosed with endometriosis Endometriosis has affected her bowel, bladder and ovary and left her with lasting damage.

What Experts Say

"Because of the pain and the complications I wasn't able to progress with my career and go to university," says Pearson. "There is a knock-on effect in terms of mental health, finances, work and fertility. So I think if people are diagnosed earlier and have a better chance of prolonged quality of life at a younger age, it could really help.

" Pearson was just 10 when her debilitating periods started, leaving her in agony. Over the years she developed painful stomach issues with everything she ate. She was told it was "part of being a woman", then it was put down to irritable bowel syndrome or stress.

She went back and forth to doctors for six years before finding a GP who said she was likely to have endometriosis. "It has been a very long journey and we definitely need more accuracy when it comes to scans," says Pearson. "We deserve something that is more consistent and reliable for patients and is non-invasive as well.

The development has drawn wide international attention, with diplomatic circles watching closely.