Next Event
A Focus on Lipedema: Bridging Gaps
February 19-20, 2026
Boston Lymphatic Symposium
Who we are
About Us
Lipedema World Alliance
Is a not-for profit association bringing together Healthcare Professionals, Researchers and Patient Associations world-wide to increase understanding of lipedema and appropriate treatments.
Lipedema World Alliance Delphi Consensus
Consensus-Based Position Paper on the Definition and Management of Lipedema: Results from the 2023 Lipedema World Congress in Potsdam
Support
Become a supporter of the LWA
Support scientific dialogue to improve understanding and treatment of people living with lipedema
Join the LWA
Join Lipedema World Alliance today and shape the future of Lipedema care together.
Healthcare Professionals and Researchers
Individual membership is open to registered healthcare professionals and researchers experienced in the field of Lipedema – unite with global experts to drive progress.
Registered Patients Associations and Scientific Associations
Membership is open to both Patient Associations and Scientific Associations, based on their local registrations covering the provision of services to those living with Lipedema or research into Lipedema.
Features
- Global Collaboration: Connect and share with experts worldwide for impactful change.
- Non-Profit Endeavor: Our commitment is for people, not profit.
- Boosted Awareness: Elevate Lipedema understanding among professionals and the public.
- Patient Advocacy: Speak up for better treatment access.
- Disease Management & Treatment: Back evidence-based Lipedema care.
- Knowledge Exchange: Share best practices and the latest research.
Benefits
- Global Network Access: Connect with pros, researchers, and associations globally.
- Involvement: Be a driving force in global Lipedema improvement.
- Patient Resources: Find guidance for those with Lipedema and their supporters.
- Research Synergy: Collaborate for advanced knowledge and treatments.
- Members-only Portal: Exclusive resources and updates await.