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
Working together we can make a change
LWA wants to create an environment where healthcare professionals from different countries and patients’ associations collaboratively explore many unanswered questions around lipedema and promote scientific dialogue in order to accomplish the goal of improving the understanding and care of people living with lipedema.
05 Oct 2023
Membership is open