by LCC | Sep 8, 2026 | Lipedema on the Internet, Social Media
If you’ve been diagnosed with lipedema—or even suspect you might have it—your first instinct is completely understandable. You go to the internet. You start Googling symptoms, scrolling social media, joining Facebook groups, watching TikToks, and reading blogs...
by LCC | Feb 26, 2026 | Misinformation, Social Media
Facebook groups can be lifelines for women with lipedema. They offer connection, shared experiences, and hope. But there’s a growing problem many women don’t recognize: Anonymous posts and comments are shaping medical and financial decisions — without accountability....
