Content Hub
Laura's Story
“I've had to explain what endometriosis is and how it affected me to so many people. This has included friends, family and colleagues. Most people think it's just a bad period.”
Endometriosis as a Professional Athlete
Charlotte Henshaw MBE, Paracanoe Paralympic Champion and Endometriosis UK ambassador shares her experience of endometriosis and navigating the disease as a professional athlete.
Endometriosis UK Statement: SMC – Relugolix, estradiol, norethisterone acetate film-coated tablets (Ryeqo®)
Endometriosis UK responds to the Government's response to the recommendations made by the Women and Equalities Committee's inquiry into "women’s reproductive health conditions"
Deepti's Story
"Some days, I have zero mobility. Other days, I’m dancing at a party. I never know what I’ll wake up to. This uncertainty has affected every aspect of my life.
But I refuse to be silent. My journey isn’t just about pain; it’s about resilience, awareness, and demanding better for those who come after me."
Urgent Government action needed to improve education for young people and healthcare practitioners: Launch of Endometriosis Action Month
Leah's Story
"It can be stressful and alienating when friends and family believe I'm exaggerating the agony or that it's "just bad periods.""
Endometriosis at Work: Rachel's Story
Endometriosis UK is pleased that Bank of Ireland pledged to become an Endometriosis Friendly Employer in 2022. Rachel Hughes shares her story of life, work and endometriosis.
Amber's Story
"When I was finally diagnosed with endometriosis, I felt a mix of relief and frustration—relief that I finally had an explanation for everything I had endured, but frustration at how long it had taken and how much I had suffered in the meantime."
