A newborn screening is a routine procedure. Shannah didn't give it much thought as she brought her daughter, Emmalyn, home from the hospital. But a late-night call set her down a road towards advocacy that she couldn't have predicted.
In this episode, we tackle the topic of increasing inclusivity in research. We're talking to three amazing women from the Accelerated Cure Project for MS. We cover the MS Minority Research Engagement Partnership Network.
Maria Thomas joins Lilly in honor of Hyperhidrosis Awareness Month to talk about her “life as a puddle” and inspiring advocacy work.
Matt Cortland joins Aaron to talk about the upcoming midterm election and what's at stake for patients.
Chris Snider, Type 1 diabetes advocate and Community Manager at TidePool joins Lilly on the Patients Have Power podcast.
Clinical research offers hope for many people, because it helps us find better treatments. Clinical trials are the core of all medical breakthroughs, and volunteer participants are the most important part of any study.
In this episode, we speak with Peter Morley, a self-described "accidental advocate" who, despite living with multiple chronic conditions, fights on behalf of all Americans for fairer healthcare access.
