My story began when I first got my period age 11. I was always in pain, missing school, etc. I was taken to the doctor who told me this was part of life.
Katie’s endometriosis experience
I would love to have another child but unfortunately, I don’t see it happening again without more surgery, and I’m not in a position to travel to a country that recognises the disease. As a woman I feel constantly let down by this country.
Michelle – Undiagnosed, symptomatic, worried.
I am one of the lucky ones…well at least that if I have endometriosis at all as I am, as yet, undiagnosed.. when I say I am lucky I mean that I got my period aged 11 and had them perfectly normally like clockwork every 28 days aside from one random agonising one age 24 that had me rolling around in pain.
Endometriosis Association of Ireland General Election Manifesto 2020
General Election 2020 provides an opportunity to request that the next Government (vote on 8th February 2020) will work with the Endometriosis Association of Ireland to help us improve the diagnosis and treatment of those living with endometriosis and adenomyosis in Ireland.
March with us! EndoMarch 2020
eam Ireland are proud to announce our 2020 EndoMarch to coincide with the worldwide events on March 28th 2020Join us in St Anne’s Park, Clontarf, Dublin. Meet up at 1.45pm to begin walk at 2pm. The route is 5km with an option to finish at 2.5km. There is no required distance, you are invited to walk whatever distance you are comfortable with.
