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!
Why Replacing ‘Lipedema’ With ‘Lipalgia’ Misrepresents the Disease
LegsLikeMine
October 27, 2026
Did you know there are two global lipedema organizations and they have a major disconnect? Did you know there’s an
