Increasing Awareness for Lipoedema

Lipoedema is still under-recognized and listed as a rare disease according to the Genetic and Rare Diseases Information Center (GARD)1. Even some healthcare professionals are not aware of lipoedema or mistake it for obesity or lymphoedema. But there is some good news: more and more scientific articles are published about lipoedema. So how does this affect you and your lipoedema?

Increasing Awareness for Lipoedema

The Past and Present

PubMed is the largest database for scientific articles, where you can find almost all internationally published research. When you search for the term "lipoedema" on this database, you'll get 54 results compared to 2.200 for lymphoedema (search date: August 2021). However, the number of published articles about lipoedema has constantly increased within the last few years. Why is this so important?

Diagnosing lipoedema can be a challenge: there are no specific blood tests or tools, and healthcare professionals must rule out other diseases that can cause similar symptoms. Commonly, people with lipoedema visit many different healthcare professionals before getting their diagnosis and starting with their treatment. Maybe you have been in a similar situation where you felt like it was an emotional roller coaster ride?

The more healthcare professionals know about lipoedema, including its causes and symptoms, the sooner it will be recognized and treated. Therefore, it is essential that lipoedema is the focus of current research.

How to Improve Lipoedoema Treatment

A group of authors published an article called "Lipedema: A call to Action" in 2019.2 In this review, the authors highlight the need for more awareness about lipoedema as a chronic disease and state: "Despite the clinical impact on women's health, lipoedema is in fact mostly unknown, underdiagnosed, and too often misdiagnosed with other similarly presenting diseases." 2

Even more important, a group of healthcare professionals from different disciplines and European countries agreed on a consensus document about lipoedema.3 This means that they sat together and developed a best practise document based on scientific evidence and their extensive experience, including all relevant treatment elements  for lipoedema. The authors also cleared up several misunderstandings or "myths" about lipoedema, which is helpful for healthcare professionals.

What You Can Do to Increase Awareness

Talking about your lipoedema also helps to increase awareness. If you are talking to other women about your lipoedema, encourage them to find out more and explore it for themselves using any of the resources listed below. You can also have a look at our article about how to explain your lipoedema to your colleagues and other people here.  



2 Buso G, Depairon M, Tomson D, Raffoul W, Vettor R, Mazzolai L. Lipedema: A Call to Action! Obesity (Silver Spring). 2019 Oct;27(10):1567-1576. doi:10.1002/oby.22597.

3 Bertsch T, Erbacher G, Elwell R. Lipoedema: a paradigm shift and consensus. J Wound Care. 2020 Nov 1;29(Sup11b):1-51. doi: 10.12968/jowc.2020.29.Sup11b.1.

Get Support From Others With Your Condition

It’s important to know you’re not alone. Join our private community and feel empowered by connecting with other lymphoedema or lipoedema patients.

Share stories and tips

with others like you

Find the right expert

for your condition
Discover more helpful tools         
Be Part of the Community and Empower Your Life
Don’t sit around and go through this in silence. Share your story. Doing that was a real eye-opener for me

Claudia Lymphoedema patient