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Colleagues thought I was faking endometriosis pain

Caitlin Parr
BBC News
BBC Dee Montague-Coast is looking at the camera smiling. She has short black hair, and is wearing a green cardigan with a sheep pattern on. There is a Christmas tree in the background, in her Newport flat.BBC
Dee Montague-Coast left her job after feeling colleagues didn't believe she had endometriosis

For women living with endometriosis, debilitating pain, fatigue and heavy periods can make it feel almost impossible to sustain a career or social life.

The only way formally to diagnose endometriosis is through invasive surgery, but getting to that stage can take on average eight to 10 years, from a patient's first GP appointment.

For women like Dee Montague-Coast, 41, the lack of evidence of disease during the diagnostic delay can lead to people not believing they are unwell, and even force them to change careers.

Now an evidence-based "symptom reporting tool" has been developed by Cardiff academics aimed at highlighting patterns that will raise healthcare providers' attention.

'Why is my endometriosis treatment not urgent":[]}