
Freya’s story: “Every time I would get a period, I couldn't move”
Freya suffered with irregular periods and pelvic pain for years. But after her sister’s diagnosis with endometriosis, Freya pursued her own.
Evie Cogley, the president of the Hula Hooping Society at Nottingham Trent University, tells us why she and the society chose to walk 100,000 kilometres to raise money for Wellbeing of Women research this year
Freya suffered with irregular periods and pelvic pain for years. But after her sister’s diagnosis with endometriosis, Freya pursued her own.
Niamh spent years suffering with debilitating symptoms of endometriosis before her own research provided some answers.
For Emma, a diagnosis of endometriosis came too late. Robbed of her fertility and life-long damage to her organs, she is now an advocate for women’s health working with organisations and workplaces to help raise awareness of this debilitating disease.