The Lipedema Foundation aims to define, diagnose and develop treatments for Lipedema, and is the largest funder of Lipedema research. The Lipedema Foundation’s work is currently focused on better understanding and defining the biology of Lipedema, and …

The Lipedema Foundation aims to define, diagnose and develop treatments for Lipedema, and is the largest funder of Lipedema research. The Lipedema Foundation’s work is currently focused on better understanding and defining the biology of Lipedema, and …

Lipedema is a chronic condition that occurs almost exclusively in women and manifests as symmetrical buildup of painful fat and swelling in the limbs, sparing the hands and feet. Women with lipedema have limited therapeutic options.

The Lipedema Foundation funds lipedema research grants for basic and translational research to define, diagnose, and develop treatments for lipedema. The Foundation emphasizes the importance of collaborative research.

Finding the right care for Lipedema can be difficult, but access to informed and compassionate healthcare professionals is critical. The Lipedema Foundation created the Provider Directory to...

Lipedema Foundation, Greenwich, Connecticut. 9,633 likes · 250 talking about this · 2 were here. Research to define, diagnose and treat Lipedema. Not a medical provider; talk to a doctor about care.

The Lipedema Foundation is funding basic and translational research projects at top-tier universities and hospitals in order to define, diagnose and treat lipedema and related conditions.

2021年10月6日 · The Lipedema Foundation is a groundbreaking organization devoted to the lipedema community in meaningful ways. Chief Science Officer Guy Eakin talks about the Foundation’s history, mission, and registry, which is key to the organization’s goal of funding research that can lead to a cure.

The Lipedema Foundation is a 501(c)(3) non-profit and 509a private family foundation with a mission to define, diagnose, and develop treatments for lipedema. We support collaborative research that addresses the basic biology, genetics, and epidemiology of lipedema.

The Lipedema Foundation is a US 501c3 non-profit and 509a private family foundation, with offices in Connecticut and Maryland. The mission of the Lipedema Foundation is to define, diagnose, and develop treatments for lipedema.