Titles coming soon!

Other Titles in the Monograph Series

LE: Lymphedema for Healthcare Professionals and Patients
(in partnership with Lymphatic Education & Research Network, LE&RN)

A Faststart Guide: Lipedema, Lymphedema & Keto Way of Eating

The Doctor & Patient Connection: Who is the Healer?

Publications in Process

The Lipedema Sourcebook: Stories, Education, and Tools for the Disease They Call FAT
Amy Thompson, PhD and Catherine Seo, PhD explore what your doctor might not know about your large hips and legs. There is a hidden lipedema epidemic. How can you come to grips with the condition, and what can you do about it.

Weight Loss for Lymphatic Disorders: Breaking the Cycle
This book brings to light the most advantageous method for weight management while focusing on the effects of nutrition on the lymphatic system.  Through her studies and clinical experience, Dr. Leslyn Keith, OTD, CLT-LANA, has come to understand that the lymphatic system needs to be fueled by proper nutrition, including a healthy intake of fat.  Ketogenic nutrition is the optimal way to promote healing, manage weight, and achieve better outcomes in those with lymphatic disorders.

Unstoppable: Lipedema, Fat, and Finding Freedom

published in collaboration with
Lymphatic Education & Research Network (LE&RN)

About The Lipedema Project

The Lipedema Project was founded in 2014 by Dr. Mark L. Smith, MD, FACS and Catherine Seo, PhD to begin the research and treatment for lipedema, a chronic fat disorder. Lipedema is a disease involving abnormal fat deposition that can result in pain, immobility, and lymphatic disturbances. Lipedema progresses over time often developing lymphedema, a chronic condition called lipolymphedema.

With obesity reaching epidemic proportions and anti-fat bias prevalent in healthcare, it becomes critical that patients are correctly diagnosed, that resources are invested in understanding this disease and how it can be treated, and that patients have the support, knowledge, and options to manage these chronic conditions.

Currently, The Lipedema Project, Inc. is a 501(c)3 non-profit organization devoted to increasing awareness and providing education, research, and treatment for lipedema through online and face-to-face programs and building community.

The lipedema documentary is available for viewing on Facebook, Lipedema – The Disease They Call FAT.
The book is available on Amazon, Lipedema – The Disease They Call FAT: An Overview for Clinicians.