Chronic illness is hard. Feeling alone shouldn’t be part of it.

Hi, I’m Megan.
I was diagnosed with lupus at 17 and spent the next 25 years pushing through flares, silence, and a healthcare system that didn’t always listen. In 2025, I finally started talking—really talking—about what it’s like to live with multiple autoimmune diseases. And to my surprise—people needed it.

I created Talk Lupus to Meg to offer emotional support, symptom hacks, and healing tools that actually feel doable—even on your worst days. What started as a few social posts turned into digital downloads, community messages, and a tiny-but-mighty brand focused on helping others feel seen, not shamed.

This page highlights a few of the resources I’ve built (and the community they’re already helping).