Lipedema – The Disease They Call FAT:
Overview for Clinicians eBook

PDF Version

Make a donation to the Lipedema Project and we will send you a copy of the PDF version of the ebook.

Donate what you can to the Lipedema Project and we will send you the ebook PDF

Suggested donation is $25 but there are those who can afford more, and those who can afford less. Donate what you can! Whatever you can afford we appreciate your generosity to our work. Thank you!

It will take financial resources to continue the work we are doing. Your donation, however small or large, will help us to continue to educate and raise awareness within the medical community and support lipedema patients.

donate to The Lipedema Project

NOTE: For larger donations, please contact us, your donation will be made to LE&RN 501(c)3 for our partnered projects moving forward.
donations@lipedemaproject.org

 

About The Friedman Center

The Friedman Center for Lymphedema Research & Treatment at The Center for Advanced Medicine at Northwell Health in New York was founded in 2013. Its focus has been on offering solutions for patients with lymphedema, a debilitating condition that occurs in many patients after cancer treatment.

The Friedman Center’s scope of care now includes treatment for lipedema, a condition that can also result in lymphedema. To that end, the Friedman Center has created the Lipedema Project, a comprehensive program to increase awareness and provide education, research and treatment for lipedema. The Friedman Center is proud to sponsor the lipedema documentary, The Disease They Call FAT, the 1st International Symposium on Lipedema, the Lipedema Think Tank, the Lipedema Solutions Forum for women with lipedema in April 2015 and this online CME eduring materials course for physicians.