For those who may not know, endometriosis is a chronic condition where tissue similar to the lining of the womb grows in other parts of the body. 1 in 10 people born female are affected worldwide. It can cause extreme pain, fatigue, and fertility struggles, yet it is often dismissed or misdiagnosed for years. By sharing my journey, I hope to shine a light on the reality of living with endometriosis, and bring us one step closer to better care, better treatment, and one day, a cure. 💛

I was diagnosed with endometriosis at just 19 years old. For many, this journey is much longer, on average, it takes 8+ years to finally receive a diagnosis. Endometriosis isn’t just my story, though. It runs in my family, and likely will affect the future generation of our bloodline, as well as millions of women across the world. Sharing this is important to me, because the more we talk about it, the more awareness we build, and the sooner we can get the help we need.

That’s why I’ve organised a charity ball, not only to raise awareness of this invisible illness, but also to raise vital funds for research and support. Endometriosis is still hugely underfunded despite affecting millions worldwide, and change can only happen if we keep pushing the conversation forward.💛