Pressing for Better Endometriosis Care in Parliament

Women living with endometriosis have endured pain, stigma and far too many delays in diagnosis for decades. This chronic condition, which affects around one in ten women and those assigned female at birth, can cause debilitating pain, fatigue and fertility challenges – yet many still wait years for a diagnosis and struggle to access the support they need.

In the House of Commons this week, I raised these concerns directly with the Minister, asking whether the Government’s new Women’s Health Strategy will lead to improved training for healthcare professionals and greater awareness of endometriosis. Too often, symptoms are dismissed or misunderstood, leaving women feeling unheard and unsupported. Earlier diagnosis and better understanding are essential to improving outcomes and quality of life.

I was encouraged by the Minister’s response and the recognition that more must be done to prioritise women’s health. The Women’s Health Strategy has the potential to drive meaningful change – from better education and training in primary care, to clearer referral pathways and faster access to specialist treatment. However, warm words must now translate into tangible action.

I will continue to press the Government to deliver real improvements and to make women’s health a genuine priority within our NHS.

Alongside raising this issue in Parliament, I have launched a survey for local residents to share their experiences of endometriosis and what they want in the upcoming Women’s Health Strategy. Hearing directly from those affected will help inform my ongoing work in Westminster and strengthen the case for change.

If you or someone you know has been impacted by endometriosis, I encourage you to take a few minutes to complete the survey and make your voice heard:

Your experiences matter, and together we can push for the improvements women deserve.

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