One of the first documentaries I saw about lipedema was Lorna’s Story. I really related to it. It’s an hour worth watching. Also, does anyone know Lorna and how’s she doing? If you know her, have her update us!
You’re Not Alone: How Support Makes All the Difference with Lipedema
LegsLikeMine
May 12, 2025
Hi friends! When you live with lipedema, people don’t always see the whole picture. They might notice the swelling or the shape of your legs—but
