East Renfrewshire’s MP has pledged support for the 1.5 million people living with endometriosis in the UK.

Kirsten Oswald has given her backing as new statistics show 75% would not go to the doctor with potential symptoms of the condition.

The data, from a survey of 2,000 UK respondents conducted by Endometriosis UK, is being released to mark Endometriosis Action Month.

Among those who said they would put off going to see a doctor in this situation, 24% said it was because they considered painful periods to be a normal part of life, while 23% said they would think it was “not serious enough to bother a doctor with.”

Ms Oswald told the Barrhead News: “Although Endometriosis affects 1.5million women in the UK, just 49% of the public are aware that endometriosis is a gynaecological health condition – a figure which drops to just 31% of men.

“There has been precious little progress in our understanding and treatment of endometriosis over the last few decades, so I am delighted to see the Scottish government funding research into the first non-hormonal drug for endometriosis with trials underway.

“I am also keen that we grow and understanding that awareness is vital to ensuring everyone recognises the signs and symptoms of endometriosis, and when and how to seek help if they are experiencing symptoms.”

Endometriosis causes cells similar to the ones lining the womb to be elsewhere in the body found elsewhere in the body.

Each month these cells react to the menstrual cycle in the same way to those in the womb, building up and then breaking down and bleeding.

Unlike the cells in the womb that leave the body as a period, this blood has no way to escape.

This leads to inflammation, pain, and the formation of scar tissue (adhesions).

The symptoms can begin at puberty, and in some cases, the impact may last for life, including after the menopause.

Common they include include chronic pelvic pain, painful periods, pain during or after sex, painful bowel movements, pain when urinating, fatigue, and difficulty getting pregnant.

Faye Farthing, head of communications at Endometriosis UK added: “Currently, it takes an average of eight years to get a diagnosis of endometriosis in the UK; without a diagnosis, treatments can’t be accessed and the disease may progress.

“While the taboo around menstrual health, and a lack of awareness of endometriosis, may contribute to this, it’s also essential that the Government takes action to ensure that healthcare practitioners recognise the symptoms, and that pathways and services are improved.

“We’re incredibly grateful to Kirsten Oswald MP for sharing their support during Endometriosis Action Month, and pledging support to ensure all those with endometriosis have access to the right care at the right time.”