Legs Like Mine the Podcast, Episode 39 Yes it's lipedema, now be careful of vultures trying to sell you something

In this episode, I talk about my experience as a patient who shares online and just some of the crazy things people have tried to sell me. But then I also share several valuable and FREE resources providing everything you need to practice solid conservative care (the cornerstone of lipedema management) on your own, without buying anything! I'm linking to a few resources for you, below: The Lipedema Foundation - a wealth of info for you and your provider, including how to diagnose, treatments, and research: www.Lipedema.orgThe Standard of Care for Lipedema in the US: Get this to your doctor. https://pmc.ncbi.nlm.nih.gov/articles/PMC8652358/pdf/10.1177_02683555211015887.pdfThe Lipedema World Alliance Delphi Consensus-Based Position Paper on the Definition and Management of Lipedema: https://www.nature.com/articles/s41467-025-68232-zAlso, www.AmericanLipedemaAssociation.org, providing education, awareness, advocacy and community for lipedema patients, providers and caregivers.