For Clinicians
While Lipedema is not rare, a proper diagnosis is often missed.
There are not many trained specialists in the field today, although that is changing. Thanks to growing patient awareness of the condition and recent inroads in scientific research, Lipedema is on its way to becoming a more widely-recognized disease.
Clinician and healthcare resources
Check out the following resources to learn more about diagnosing and treating Lipedema:
How is Lipedema diagnosed? In this video Lipedema Clinical Assessment, Sarah Whitehead, MN, ARNP, walks through a real clinical assessment using a patient model and LF’s Clinician’s Guide. Sarah explains what she looks for, the key signs and symptoms, and how she makes decisions during an exam.
If you’ve ever wondered what you might expect during a Lipedema evaluation, this is a helpful place to start.
About the Lipedema Foundation
The Lipedema Foundation aims to define, diagnose, and develop treatments for Lipedema and is the largest funder of Lipedema research. Our work focuses on understanding the biology of Lipedema and improving diagnosis. We have provided $13.6 million in research funding, supported projects globally, and established the LF patient registry with over 5,550 participants. We also work to increase awareness through educational materials, conferences, social media outreach, and healthcare provider education.