Research that matters –
For a better future with lipedema
The European Society for Lipoedema e.V. promotes research, networking, and education—for better care for women with lipedema throughout Europe.
Working together for knowledge, awareness, and better care for lipedema
The European Society for Lipoedema (EuSoLip) was founded in 2017 with the aim of pooling and disseminating scientific knowledge about lipoedema and giving patients across Europe a voice.
Under the leadership of Dr. Dominik von Lukowicz and board members Dr. Katrin Lossagk and Dr. Michael Sauter, the focus is on promoting research, care, and exchange.
Based in Munich, EuSoLip is an independent association that acts as a point of contact for medicine, science, politics, and the public—always serving the interests of affected women.
Helmholtz Munich – Research for a healthier society
The current research focus is on the detailed analysis of pathophysiological mechanisms associated with adipose tissue dysfunction. The study centers on the functional characterization of adipose tissue in lipedema and the identification of circulating biomarkers that contribute to the development and progression of the disease.
Dr. Pamela Nono Nankam
Postdoctoral researcher at the Helmholtz Institute for Metabolism, Obesity and Vascular Research (HI-MAG), Helmholtz Center Munich at Leipzig University and Leipzig University Hospital AöR, Leipzig, Germany
News & Dates
February 19–20, 2026
Boston (USA)
March 6–7, 2026
Online
April 17-19, 2026
Online
September 23–26, 2026
Frankfurt am Main
October 3rd, 2026
Vienna (AT)
October 15-17, 2026
Leipzig (DE)
October 15-19, 2026
Antalya (TUR)
October 23-25, 2026
Niagara Falls (CAN)
Our goal: to conduct research, raise awareness, and make improvements together—for those affected by lipedema.
Strengthen research
We support interdisciplinary studies on the development and treatment of lipedema and actively promote the advancement of medical knowledge.
Enabling knowledge transfer
The association creates spaces for exchange and continuing education—for treating physicians and medical professionals across Europe.
Build networks
We connect patients, professionals, and institutions across borders—for a strong European community.
Dialogue with the healthcare system
As an independent association, we are the point of contact for industry, politics, and science—with the aim of improving supply in a sustainable manner.
Understanding lipedema – for diagnosis, research, and education
Support with diagnosis is provided by the Munich Lipedema Score (MLS). All lipedema symptoms are taken into account in the diagnosis. These include medical history, symptoms, and morphology. A maximum score of 40 can be achieved under these criteria. This results in advanced lipedema.
Dr. Dominik von Lukowicz from LIPOCURA® presented the Munich Lipedema Score for the first time in 2021 at the major annual conference of the German Society of Plastic, Reconstructive, and Aesthetic Surgery (DGPRÄC) in Hamburg. The MLS was developed by experienced plastic surgeons Dr. von Lukowicz, Dr. Lossagk, Dr. Wagner, and Dr. Bauer to improve the verification and classification of lipedema.
We are part of pioneering research projects at universities and clinics in Europe:
A short path to more knowledge, help, and exchange

Contact request or guide – request free of charge
Our current guide provides you with a comprehensive overview of symptoms, diagnostics, treatment options, and current research approaches. Simply fill out the contact form—we will send you the guide either as a PDF download or, if you prefer, as a printed version by mail.