Pre-COVID: Recognizing the Value of Clinical Research Jen recognized the power of clinical research long before the COVID-19 pandemic struck. When her son was born, she immediately signed him up to be in the University...
Jamie Koll, famous foodie instagrammer and rare disease patient advocate shares her experience participating in a clinical trial during the COVID pandemic.
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.
Chris Snider, Type 1 diabetes advocate and Community Manager at TidePool joins Lilly on the Patients Have Power podcast.
In this episode, we speak with Arthritis Ashley - a writer, patient advocate, and a powerhouse voice for those who live with chronic conditions, about her journey and ongoing projects.
Molly talks to Lilly about life with rare diseases, getting a hysterectomy in your 20s, and what happens when you heart is in the wrong place.
