https://www.podbean.com/media/share/pb-7szd4-1ad5a45

What does it actually look like to walk into a state legislature and fight for rare disease patients? This episode, I share what I learned from two days advocating at the NC Legislature with the Everylife Foundation for Rare Diseases — what surprised me about how state lawmakers think, why the knowledge gap isn’t what I expected, and what a single staffer’s comment about a stack of one-pagers taught me about what advocacy actually requires. Plus: three NC bills that still need your voice.