FIND A DOCTOR: Lipedema-Lipoedema-Lipödem Provider Worldwide Directory

If you are looking for effective strategies to treat lipedema & lymphedema be sure to scroll down.

This Lipedema/Lipoedema Provider Directory has been compiled by the worldwide network of lipedema ladies. Our main goal is to provide resources that can support you in your journey with lipedema. We do not recommend any particular provider. Providers listed were added by someone who has been treated by or knew of them.

We support conservative care inclusive of nutrition, movement, and complete decongestive therapies. While we do not support surgery as a first-line treatment, surgeons are listed for diagnosis only. This list is not intended to be a referral list for surgery.

If you have a provider or are a provider, who is diagnosing, treating, or caring for lipedema patients and would like to be added to the directory, please contact [email protected] with information and we will follow up with you.

American Lymphedema Framework Project (ALFP) provides a search directory to locate trained specialists in lymphedema management. These therapists are generally trained in lipedema as well and can be very helpful for both diagnosis and treatment. DIRECTORY HERE

Special thanks to all the lipedema ladies who ongoingly contribute to this directory. We update this directory regularly.

We are inviting you to our Heart-to-Heart
Virtual Community Event

Learn the formula to living well and use it to:

✨ Insightful Workshops: Engage in thought-provoking workshops led by renowned experts in the fields of Nutrition, Lipedema, and Lymphedema. Gain practical tools to navigate your unique health challenges.

✨ Supporting Materials: Access to a wealth of tools and resources that are curated to help you develop your individualized nutritional plan.

✨ Interactive Q&A Sessions: Connect directly with our speakers during live Q&A sessions. Get answers to your burning questions and gain clarity on your path to joyful nutrition.

✨ Community Support: Join a community of like-minded individuals who understand your journey. Share experiences, exchange tips, and build a support network that lasts beyond the event.

Yes, It Really Is Possible!


CLICK HERE OR IMAGE BELOW

The Lipedema Project Virtual Conferences Heart to Heart Events