Robert Largan MP is raising awareness for the 1.5 million women living with endometriosis in the UK to mark Endometriosis Action Month (March), as new statistics show that 75% would not go to a doctor with potential endometriosis symptoms. The research also shows that just 49% of the public are aware that endometriosis is a gynaecological health condition – a figure which drops to just 31% of men.
The data, from a survey of 2,000 UK respondents conducted by Endometriosis UK, is being released to mark of 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”.
This common, sometimes debilitating but often-ignored disease affects 1 in 10 women and those assigned female at birth, and can impact all areas of life include mental health, career and relationships.
Common symptoms of Endometriosis include: chronic pelvic pain; painful periods; painful bowel movements; pain when urinating; fatigue; and difficulty getting pregnant. Those with one or more of these symptoms may want to keep a pain and symptoms diary to help them in discussion with their doctor to help diagnosis, Endometriosis UK advises. Getting an earlier diagnosis of endometriosis allows access to treatment and management options; without this, the disease may progress.
The data also shows that half (51%) of women would feel comfortable talking about periods with their parents or guardians. The figures varied when it came to talk to their spouse (73%), friends (67%), colleagues (33%), medical professionals (72%) or ‘someone I have just met’ (15%) - meaning many feel uncomfortable with such discussions.
The symptoms of endometriosis can begin at puberty, and in some cases the impact may last for life, including after the menopause.
Robert Largan, MP for High Peak, commented:
“Endometriosis is a common, long-term condition, affecting 1.5million women in the UK, that can have a significant impact on a woman’s life. I am aware of and sympathise with the hardships faced by women who experience severe symptoms.
“I was pleased to be able to speak in the Westminster Hall Debate on endometriosis and polycystic ovary syndrome in the Westminster Hall Debate on endometriosis and polycystic ovary syndrome in tribute to the late Sir David Amess MP. During the debate I was able to highlight to work of my constituent, Maddy Howarth, who has campaigned tirelessly to raise awareness of endometriosis to ensure that other women do not have to go through the pain that she has endured.
“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. Yet, just 49% of the public are aware that endometriosis is a gynaecological health condition – a figure which drops to just 31% of men.
“I welcome the work of Endometriosis UK to raise awareness of this disease, as well as providing sufferers with further information and access to clinical trials and the latest research.”
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 Robert Largan 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”.
