video1.0<iframe src="https://www.loom.com/embed/11c3f8d4b7d44ddd86c005463e679202" frameborder="0" width="1920" height="1440" webkitallowfullscreen mozallowfullscreen allowfullscreen></iframe>14401920Loomhttps://www.loom.com14401920https://cdn.loom.com/sessions/thumbnails/11c3f8d4b7d44ddd86c005463e679202-684c3f180288213a.gif600.767In this video, I share my journey as Delaware's Insurance Commissioner and the importance of improving access to diagnosis and treatment for Lyme disease. I reflect on my daughter Hannah's struggle with severe symptoms and our pursuit of effective treatments, which ultimately led to her finding relief through a therapy administered outside the U.S. I emphasize the need for continued education among healthcare providers regarding Lyme disease and the challenges families face with insurance coverage for non-FDA approved therapies. I encourage all viewers to advocate for better insurance policies and to support ongoing research in this critical area. Together, we can make a difference for families affected by Lyme disease.