by EA Admin | May 15, 2021 | Endo stories
Sally Power shares her experience living with misdiagnosed stage 4 endometriosis; hoping to spread awareness to the general public, and inspire other EndoWarriors to seek help and not tolerate their pain. For 35 year old Sally Power from Darlington Point— a small town...
by EA Admin | May 1, 2021 | Endo stories
Kate Muir was 15 years old when she realised something wasn’t quite right. With heavy periods and clotting, her period pain was so bad, she’d pass out. But when she sought help from the medical system, they told her it was all in her head. “They said my anxieties were...
by EA Admin | Apr 25, 2021 | Endo research and education
My name is Olivia-Jane Gaskell. I am a 41 year-old mum of two daughters, a wife to an amazing and very supportive husband and I am 6 months post-op from having a hysterectomy due to my recent diagnosis of Adenomyosis in September 2020. I have always suffered from...
by EA Admin | Apr 10, 2021 | Endo stories
I’ve seen quite a number of doctors in my time. There was a stage where I seemed to be collecting ‘ologists’ left right and centre. While I’ve been fortunate and privileged enough to have experienced some exceptional care – which I am forever thankful for, I’ve...
by EA Admin | Mar 27, 2021 | Endo research and education, Endo support
Endometriosis now affects approximately 1 in 9 women (1). This amounts to around 200 million women worldwide with diagnosis taking anywhere from 7-12 years (1). Irritable bowel syndrome (IBS) and endometriosis share many common features- low grade inflammation,...
