Hey there, I’m Elyn (or Ellie).

I’m an endo warrior, a word nerd, and an advocate for disability awareness. Living with endometriosis means navigating constant pain, fatigue and a healthcare system that often doesn’t listen. I started this blog to document what daily life is like when your body’s in revolt and to carve out a community where we can talk about it honestly.

When I’m not curled up with a heating pad, you’ll find me writing, dancing badly in my kitchen, or researching the latest medical studies like a detective. I believe in science, hugs, and the power of sharing our stories. My goal here is to blend personal experience with practical resources, connect with fellow chronically ill folks, and offer caregivers and practitioners a window into our reality.

You deserve validation and support, not gaslighting. Together we’ll challenge myths, debunk ableism, celebrate small victories, and hold space for the hard days. Grab a mug of tea, make yourself comfortable, and let’s get to know one another.