Uniting for Change: The Power of the Lipedema Community

Hi friends! Living with lipedema can be a challenging and often isolating experience. Many patients struggle for years to get a proper diagnosis, let alone find effective treatments or insurance coverage. But there’s strength in numbers, and it’s time for the lipedema community to come together and make our voices heard! In recent years, we’veContinue reading “Uniting for Change: The Power of the Lipedema Community”

June 11 is World Lipedema Day – Share Your Story. Amplify our Voices

Hi Friends!  Today is World Lipedema Day.  Share your story. Why We Need to Fight for Lipedema Awareness June 11th marks World Lipedema Day, a crucial reminder of the invisible struggle faced by countless individuals worldwide, predominantly women, living with this chronic and debilitating condition. Lipedema, a disorder of the connective tissue, is often misunderstood,Continue reading “June 11 is World Lipedema Day – Share Your Story. Amplify our Voices”

So, I Wrote a 300 Page Book of Lipedema Lady Art in One Day, and It’s Pretty Great!

Hi friends! To get this party started, if you’d like to see the book and even purchase a coffee table version, here’s the link to the book I’m talking about:  https://amzn.to/3Nrm3yC Now we can start.  I’ve been researching an upcoming set of posts about how society can support women with lipedema.  One of the ideasContinue reading “So, I Wrote a 300 Page Book of Lipedema Lady Art in One Day, and It’s Pretty Great!”