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Standard of Care for Lipedema in the United States: best resource for information (upload to your patient portals)

FDRS provides education and resources to patients, physicians, therapists, and researchers. Hosts annual conference for all.

www.fatdisorders.org​

Dr. Karen Herbst is one of the most knowledgeable people re. Lipedema and other loose connective tissue disorders.

​​​​​www.lipomadoc.org

The Lipedema Foundation: supports research that addresses biology, genetics, and epidemiology of Lipedema 

https://www.lipedema.org