Liz Jarvis

I thank my hon. Friend for his important point. Women should not have to fight to get the treatment they need. I have also heard from Kelly, who told me: “Every month I am in debilitating pain and it is soul destroying. I cannot take days off work every month and there is nothing I can do but suffer. It affects my work, relationships and is ruining my life.” Then there is Lucy, who has worked in the NHS for 20 years and is now a clinical nurse specialist for endometriosis. She told me: “I grew up during a time when endometriosis was never mentioned. I was told that periods are painful, so the monthly debilitating pain and heavy periods I experienced were normalised.” She was finally diagnosed with endometriosis in her mid-30s. Women should not have to put up with the pain of this debilitating disease, and I urge the Government to take urgent action to tackle the postcode lottery for endometriosis care, address gynaecological waiting lists, improve training and awareness among healthcare professionals, and ensure full implementation of NICE guidelines, with clear referral pathways, so that no woman has to suffer for years without answers or support. I am sure the Minister agrees that addressing delays in diagnosis, gaps in care and inequalities in access are of the utmost importance. More broadly, this debate highlights a wider crisis in women’s healthcare—from the scandal of unsafe maternity units to the nearly 750,000 women currently on gynaecology waiting lists, over 30% of whom have waited for more than a year from referral to treatment. It must be addressed, because women are being failed and society suffers as a result. I hope the Minister also agrees that access to mental healthcare should be expanded for women with endometriosis. Dismissed symptoms and diagnosis delays left 98% of respondents to an Endometriosis UK survey reporting an impact on their mental health, and 63% of respondents describing that impact as significant. I hope that the Minister will consider expanding mental healthcare provision to give the countless women dealing with the psychological toll of endometriosis the support that they need. We need a system that is fit for purpose, which validates women, takes their symptoms seriously and provides timely, compassionate and effective care. I do not think that that is too much to ask. Alongside investment in the workforce, improved access to GPs, continuity of care and a step change in research to address painful conditions that women have suffered from for far too long without remedy, are all absolutely essential. Ultimately, this debate is about delivering better outcomes and proper support for those affected by endometriosis. I hope that the Government will tackle this issue, showing clear leadership and transparency, to ensure that every woman with endometriosis has access to the right care at the right time.