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Closed Fund mandatory endometriosis training for all NHS staff

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We think every person with endometriosis is being failed.
Endometriosis diagnosis can take 8-10 years not because it is a complex process, but because we feel we are ignored by every medical professional we encounter. Even when diagnosed, we feel professionals do not understand the condition.

My experience with endometriosis has been harrowing, but unfortunately this is typical for many sufferers in the UK.

Nobody wants a life changing diagnosis. Endometriosis is associated with fertility problems, chronic pain, and life-threatening complications. The news was broken to me by being handed a scrap of paper with the word “adenomyosis?” (spelt incorrectly) scrawled at the bottom. Even after diagnosis, the surgery and lack of aftercare I’ve received has been traumatising.

Nobody should have to experience this. I feel that with increased education and awareness of endometriosis, other people might be spared the pain, indignity and trauma I have experienced.

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  • Related activity

    Women’s Health Strategy: Endometriosis and Fibroids - debate in Parliament

    On 5 March, Abena Oppong-Asare MP led an adjournment debate in Parliament entitled 'Women’s Health Strategy: Endometriosis and Fibroids'.

    Minister for Secondary Care Karin Smyth MP responded on behalf of the Government.

    Explainer

    Adjournment debates give an MP the opportunity to debate a topic they choose, and receive a response from the Government.

    They are a way to:

    • raise awareness of an issue
    • seek to influence government policy
    • put the views of the MP and the Government on record.

    They do not involve a vote on a particular action or decision.

    The debates take place at the end of each day in the House of Commons. They last for 30 minutes.

    See our visual explainer on how these debates work.

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    This petition will stay open until 12 December 2025.