Lipedema awareness


How You Can Increase Lipedema Awareness

By | Lipedema awareness

Today, I’m going to talk about the International Lymphatic Disease and Lymphedema Patient Registry & Biorepository. It is a crucial vehicle for research and increasing awareness about lymphedema and lipedema. The information I’ll cover in this post has been taken directly from the Lymphatic Education & Research Network (LE&RN) website….

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News about lipedema spreading around the world!

By | lipedema, Lipedema awareness | No Comments

Sara Bramblette, Lipedema and Lymphedema Health Activist, writes about the different stages of being newly diagnosed! Cara Jones from Wales, UK, tells her story about diagnosis and planned surgery in Germany. stay tuned for more to come…

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