Hey there, fellow warriors and allies! I’m Elyn, and I created this space to share the raw, real experience of living with endometriosis. If you’ve ever felt like you’re yelling into the void about your pain, fatigue and frustration – you’re not alone.

On this blog I’ll be opening up about my journey with endo – the good days, the bad days, and the weird in‑between. I’ll also dive into what it’s like to navigate a complex medical condition in a world that often pretends chronic illness doesn’t exist. We’ll talk ableism, accommodations, medical gaslighting and all those unseen battles we fight every day.

But this isn’t just a personal journal. I’m also here to educate and advocate. You’ll find resources for caregivers, family and friends who want to understand what we’re going through. I’ll highlight ways health‑care practitioners can provide better, more compassionate care for endo patients.

Together we’ll challenge myths, advocate for disability awareness and build a community that supports one another. Feel free to share your own stories, tips and questions in the comments.

Thanks for joining me on this journey. Let’s make some noise and change the conversation around endometriosis and disability.

– Elyn (or Ellie, if you prefer)