Hi friends! As someone who has been living with lipedema for years and advocating for better awareness and understanding of this condition, I can’t stress
Hey there, my dear friends and fellow lipedema warriors! Please share this post far and wide in the community right now. I hope this finds
Hi friends, As I prepare for Lipedema Awareness month, which starts in just a few days now, I continue to put more foundational information out
Hi friends! As I continue to prepare for Lipedema Awareness month, I’m really excited to see what the other ladies in the Lipedema Community have
Hi friends, this post is intended to share with physicians and healthcare providers, whom you’ve worked with to get a lipedema diagnosis, and have been
Hi friends! As you can tell, I’m gearing up for Lipedema Awareness Month, and I encourage you…ask you, to participate using your skills, interests, and
Hi friends, With our condition affecting around 11% of women, the chances are you know someone who has lipedema. It might be your mom, sister,
Hi friends! Can you believe June is just around the corner? You know what that means – it’s time to get ready for Lipedema Awareness
Hi friends! Let’s talk about fibrosis. We don’t talk about it enough and its a pretty big, actually MAJOR issue for women with lipedema. This
Hi friends! I’ll be attending Fat Disorders Resource Society again this year. And for the second year in a row, to celebrate this important event,
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LegsLikeMine supports the 11% of the women in the world, who have lipedema.
