Fund mandatory endometriosis training for all NHS staff
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.
Signatures
987
signatures
Government response threshold (10,000) · 987/10,000
Debate threshold (100,000) · 987/100,000
- 12 DEC 2025Petition closedFinal total: 987 signatures
- 12 JUN 2025Petition opened for signatures
Background
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.