Ms Abena Oppong-Asare

Endometriosis, fibroids and related gynaecological conditions ruin the lives of millions of women, yet these conditions remain undiagnosed, misdiagnosed, dismissed or mistreated within the health system. Women are told to shut up and stop complaining. We are fobbed off. We experience shameful delays. We are left in pain. My argument today is simple. We need the forthcoming women’s health strategy to address these conditions head-on, listen to women, tackle the taboos, and create timely and effective treatment. One in 10 women suffer from endometriosis. It is a painful, debilitating condition, found in every community, workplace and family. That statistic means that at least 20 women Members in this current Parliament could be suffering from endometriosis. Despite being widespread, it remains misunderstood and dismissed, yet it ruins women’s ability to learn, earn, have sex, have children and live a normal, healthy life. It destroys mental health. In recent years, there has been greater awareness and a wider discussion of the impact of the condition, led by public figures such as the BBC’s Emma Barnett, and sparked by this year’s BAFTA-winning short film, “This Is Endometriosis”, which I hope to host a screening of in Parliament soon. In this House, I commend the great work of the chair of the all-party parliamentary group on endometriosis, my hon. Friend the Member for Bathgate and Linlithgow (Kirsteen Sullivan), and the Chair of the Women and Equalities Committee, my hon. Friend the Member for Luton North (Sarah Owen). Millions of women, however, are still being failed by the NHS and wider society. There is still a lack of appreciation of the true nature of the disease, a lack of suitable support throughout the worlds of education and work, and stigma associated with the symptoms, which include heavy bleeding and intense, blinding pain. The average wait for diagnosis is nine years and four months, according to the latest report, launched this week, by the charity Endometriosis UK. The report highlights that diagnosis times are getting worse, not better. March is Endometriosis Action Month. It is vital that we use this opportunity to act now for the benefit of those suffering today, and those who will suffer long into the future. Sadly, even with a diagnosis, there is no cure—just pain management.