When I was diagnosed with endometriosis one year and a half after I was diagnosed with MS, I was surprised to learn that, unlike MS, endometriosis is not a rare disease. Yet there’s less talk about endometriosis, and there is for sure less research into finding a cure or finding ways to improve the lives of millions of women around the world. I was taken aback by how little is currently being done to understand what causes it, why and how it develops and how it can be prevented or managed once it’s settled. It’s like doctors just decide to cut you up to remove the endometriosis tissue, send you home, and do it all again when more unwanted tissue grows. Like we were needle felting pads or something.
Below is the trailer of Endo What, a documentary aiming to raise awareness to some of these issues. And take a look at this insightful Guardian article which lets you know more about it. And then let’s all say “Enough already!”