Let’s make Lipedema a household word.

For Lipedema Awareness Month, the Lipedema Foundation is offering resources to help get the word out.

Social Shareables

Help us raise awareness about Lipedema! Share our content with your network. This selection of shareable images can be used on Facebook, Instagram, Twitter and Pinterest. Right click on any image, save and share on social media.
Use hashtag: #lipedemaawarenessmonth2022

Check out our resources:

LF Registry

Sign up for the LF Registry! Your participation in our Registry helps support scientific research to improve the life of Lipedema patients. Sign up here.

Clinical Trial Finder

Participate in research studies If you want to learn about clinical research studies that are seeking Lipedema patients, check out our LegWork Clinical Trial Finder.

Legato Library

Looking for Lipedema research? Our digital Legato Library makes it easy to search for Lipedema research by keyword, topics, and more. Find research papers here.

Share our free brochure with friends, family and clinicians

The Lipedema Foundation’s What is Lipedema? brochure answers key questions about the condition. Share copies with friends, family and clinicians! The brochure is available in English, Spanish and German. All three versions can be downloaded here. You can also order free copies that take two to three weeks to be delivered. To order, please fill out this form and include an address and quantity.

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Sign up for our e-newsletter

Subscribe to our newsletter to receive more detailed updates, both for Lipedema Awareness Month and beyond!