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Lipedema awareness

lipedema research and 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! http://blog.wegohealth.com/2014/09/15/the-phases-of-a-lipedema-diagnosis/ Cara Jones from Wales, UK, tells her story about diagnosis and planned surgery in Germany. http://www.newsnorthwales.co.uk/news/138229/wrexham-mum-tells-of-pain-over-tree-trunk-leg-condition.aspx stay tuned for more to come…

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