Kate Pecora is an impassioned advocate for rare and chronic disease, disability justice, and healthcare policy. She is diagnosed with Spinal Muscular Atrophy Type III, and is lives in Boston, Massachusetts. Kate is currently (e)traveling across the country in search of the most compelling stories of patient access, affordability, and quality. Want to share your story and join the Patient’s Rising Community? Reach out to Kate for opportunities to join her weekly blog posts and interviews on the Patients Rising Podcast.